Ahmedabad Healthcare Jobs

Why This Role MattersPharmacovigilance systems play a vital role in ensuring that drug safety information is properly collected, managed, and reported to regulatory authorities. A Pharmacovigilance System Specialist helps maintain the integrity of safety databases and supports compliance with global pharmacovigilance regulations. This role ensures that adverse event data is handled accurately and efficiently, allowing pharmaceutical companies to monitor product safety and protect patient health.At Amneal Pharmaceuticals, professionals in this role contribute to maintaining strong pharmacovigilance operations by supporting safety database management, ensuring regulatory compliance, and facilitating effective reporting processes.Job DescriptionThe Pharmacovigilance System Specialist is responsible for managing pharmacovigilance systems, particularly the Oracle Argus Safety database. The role involves system configuration, workflow setup, user access management, compliance monitoring, and reporting activities.The professional works closely with pharmacovigilance teams, regulatory departments, and IT support teams to ensure that drug safety databases operate smoothly and comply with global pharmacovigilance guidelines such as ICH and GVP. The position also includes system validation, documentation, troubleshooting, and providing training or support to team members who use the pharmacovigilance system.Key Features of the RoleThis role provides exposure to advanced pharmacovigilance systems and global safety regulations. Professionals in this position gain experience in database administration, safety data management, and compliance monitoring.The role also offers opportunities to collaborate with multiple departments, including drug safety operations, regulatory affairs, and quality assurance teams. It is ideal for candidates interested in combining pharmacovigilance knowledge with technical system management.Responsibilities• Configure and maintain pharmacovigilance systems such as Oracle Argus Safety.• Manage user access, roles, and permissions within safety databases.• Set up workflows and system configurations according to pharmacovigilance requirements.• Monitor compliance with global pharmacovigilance regulations including ICH and GVP guidelines.• Generate safety reports and maintain system documentation.• Support system validation and ensure regulatory compliance of pharmacovigilance databases.• Provide troubleshooting support for pharmacovigilance system issues.• Ensure accuracy and quality of pharmacovigilance data entry.• Maintain documentation and ensure adherence to Standard Operating Procedures (SOPs).• Conduct training sessions and provide support to pharmacovigilance team members.Required QualificationsEducational RequirementsCandidates should possess one of the following qualifications:• Bachelor’s degree in Life Sciences• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)• Master’s degree in Life Sciences or related healthcare fieldExperience and SkillsCandidates should have knowledge or experience related to pharmacovigilance systems and drug safety processes.• Strong knowledge of pharmacovigilance processes• Experience with Oracle Argus Safety system• Understanding of ICH and GVP pharmacovigilance regulations• Database administration and configuration skills• Analytical and troubleshooting abilities• Attention to detail and accuracy in safety data management• Ability to follow SOPs and maintain proper documentation• Strong communication and training skills• Organizational and time management abilitiesSalary InsightsThe salary for a Pharmacovigilance System Specialist in India varies based on experience, organization size, and technical expertise.• Salary rang: ₹ 4.5 -₹ 8 LPA (estimated)Additional benefits may include health insurance, professional development programs, performance incentives, and career growth opportunities.Company OverviewAmneal Pharmaceuticals is a global pharmaceutical company focused on developing, manufacturing, and distributing high-quality generic and specialty medicines. The company operates across several international markets and is known for its commitment to affordable healthcare solutions and regulatory compliance. With advanced research, manufacturing, and pharmacovigilance systems, Amneal continues to expand its presence in the global pharmaceutical industry while maintaining strong standards for product safety and quality.FAQs1. What does a Pharmacovigilance System Specialist do?A Pharmacovigilance System Specialist manages drug safety databases, supports regulatory compliance, and ensures accurate handling of adverse event data.2. What is Oracle Argus Safety?Oracle Argus Safety is a widely used pharmacovigilance database designed for managing adverse event reporting, safety case processing, and regulatory submissions.3. Is pharmacovigilance system experience necessary?Experience with safety databases such as Argus Safety is highly preferred for this role, especially for system configuration and administration tasks.4. What career opportunities are available after this role?Professionals can advance to roles such as Senior PV Systems Specialist, Pharmacovigilance Operations Manager, Drug Safety Manager, or Global Safety Systems Lead.Application Tips• Highlight experience with pharmacovigilance databases like Oracle Argus Safety.• Demonstrate knowledge of ICH and GVP safety regulations.• Emphasize technical skills related to database administration and system configuration.• Mention experience with SOP compliance, documentation, and system validation.• Showcase communication skills and the ability to train or support pharmacovigilance teams.

Why This Role MattersMedical Advisors play a critical role in bridging scientific knowledge with strategic business decisions in the pharmaceutical industry. This role ensures that medical strategies, product communication, and clinical insights are aligned with patient needs and evidence-based practices. By collaborating with healthcare professionals (HCPs), key opinion leaders (KOLs), and internal teams, Medical Advisors help shape responsible product positioning, support new product launches, and strengthen scientific credibility within therapeutic areas such as cardiology, diabetes, neurology, gastroenterology, gynaecology, and orthopaedics.Job DescriptionA growing Medical Affairs team is hiring Executive – Medical Affairs and Assistant Manager – Medical Affairs roles based in Ahmedabad. The position focuses on medico-marketing strategy, clinical research coordination, scientific communication, and collaboration with cross-functional teams to support pharmaceutical brands and patient-focused healthcare initiatives.Key Features of the Role• Job Title Options: Medical Advisor / Executive – Medical Affairs / Assistant Manager – Medical Affairs• Work Location: Ahmedabad• Department: Medical Affairs / Medico-Marketing• Experience Required: 1–3 years (Executive) | 4–6 years (Assistant Manager)• Qualification: Pharm.D or M.Pharm• Industry: Pharmaceutical / Healthcare• Travel Requirement: 30–40% for meetings and field interactionsResponsibilities• Provide medical and scientific input for product strategies and brand development.• Gather insights from Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs).• Collaborate with marketing and sales teams to develop patient-focused strategic plans.• Support new product launches through scientific materials such as monographs, FAQs, and presentation slides.• Review and validate visual aids (VA) and leave-behind literature (LBLs).• Organize and participate in advisory board meetings and KOL interactions.• Manage medical information requests and provide scientific responses.• Lead non-interventional studies (NIS) and clinical research projects from conceptualization to publication.• Prepare study documents, coordinate ethics committee approvals, and oversee investigator meetings.• Ensure accurate documentation and publication management related to pharmaceutical brands.• Work with cross-functional teams to ensure alignment between scientific evidence and commercial strategy.Required Qualifications• Doctor of Pharmacy (Pharm.D) or Master of Pharmacy (M.Pharm).• Strong understanding of medico-marketing and pharmaceutical product strategy.• Experience interacting with healthcare professionals and key opinion leaders.Educational RequirementsCandidates must hold one of the following degrees from a recognized institution:• Pharm.D (Doctor of Pharmacy)• M.Pharm (Master of Pharmacy)These qualifications provide the scientific foundation required for handling clinical data, medical communications, and pharmaceutical research initiatives.Experience and Skills• 1–3 years of medico-marketing experience for Executive role.• 4–6 years of experience managing medical strategy for Assistant Manager role.• Knowledge of therapeutic areas such as cardiology, diabetes, neurology, gastroenterology, gynaecology, and orthopaedics.• Strong communication and presentation skills.• Ability to work with cross-functional teams in a fast-paced environment.• Experience managing clinical studies, investigator meetings, and scientific publications.• Strong analytical and problem-solving abilities.• Ability to prioritize tasks and manage multiple projects simultaneously.Salary InsightsThe compensation for Medical Affairs roles typically varies based on experience and expertise. Industry standards for similar roles in India range from mid-level to senior-level salary packages depending on the position (Executive or Assistant Manager), therapeutic expertise, and previous industry experience.Company OverviewThe hiring organization is expanding its Medical Affairs team to strengthen scientific engagement and research-driven strategies in the pharmaceutical sector. The company focuses on evidence-based product development, medical education, and collaborative engagement with healthcare professionals to improve patient outcomes.FAQsQ1. What qualifications are required for this role?Candidates must have a Pharm.D or M.Pharm degree.Q2. Is prior medico-marketing experience required?Yes. Executive roles require 1–3 years of experience, while Assistant Manager roles require 4–6 years.Q3. Which therapeutic areas are relevant for this role?Cardiology, diabetes, neurology, gastroenterology, gynaecology, and orthopaedics.Q4. Does the role involve travel?Yes, approximately 30–40% travel may be required for meetings and professional interactions.Q5. Where is the job location?The role is based in Ahmedabad.Application Tips• Highlight medico-marketing and clinical research experience in your resume.• Mention therapeutic area expertise if applicable.• Include examples of working with KOLs or conducting medical education programs.• Demonstrate experience in preparing scientific documents and product launch materials.• Emphasize communication skills and ability to collaborate with marketing, sales, and research teams.

Why This Role MattersThe Quality Control Executive – Ayurvedic Division plays a vital role in ensuring the safety, purity, and consistency of Ayurvedic and herbal products. This position ensures that raw materials, in-process samples, and finished goods meet regulatory and quality standards before release.By maintaining laboratory accuracy, ensuring compliance with AYUSH and GMP regulations, and supporting audit readiness, the role directly contributes to product integrity and consumer trust in herbal healthcare solutions.Job DescriptionSunrise Remedies Pvt. Ltd. is hiring a Quality Control Executive – Ayurvedic for its Santej, Ahmedabad facility. The selected candidate will be responsible for routine testing, laboratory instrument handling, documentation control, and regulatory compliance within the Ayurvedic manufacturing unit.The role requires hands-on experience in quality testing of herbal products, microbiological analysis, stability studies, and collaboration with Production and QA teams for quality investigations.Key Features of the Role• Position: Quality Control Executive – Ayurvedic• Department: Quality Control – Ayurvedic• Location: Santej, Ahmedabad (Gujarat)• Experience Required: 1–2 years (Ayurvedic / Herbal QC)• Qualification: B.Sc | M.Sc | B.Pharm (Ayu) | M.Pharm (Ayu) (Preferred)• Industry: Ayurvedic / Herbal Pharmaceutical ManufacturingAdditional Benefits:• Transportation facility (as per company route coverage)• Mediclaim facility• Company-provided food facilityKey Responsibilities• Conduct routine quality checks of Raw Materials (RM), Packaging Materials (PM), in-process samples, and Finished Goods (FG)• Ensure compliance with AYUSH regulations, GMP, ISO standards, and applicable guidelines• Operate and calibrate laboratory instruments such as HPTLC, UV-Vis Spectrophotometer, and pH meters• Prepare and maintain SOPs, test reports, Certificates of Analysis (COAs), and product specifications• Conduct microbiological testing and stability studies• Collaborate with Production and QA teams for troubleshooting and quality investigations• Handle Non-Conformance Reports (NCRs) and support CAPA implementation• Review Batch Manufacturing Records (BMRs) for compliance• Support regulatory audits (AYUSH, FSSAI, WHO-GMP) and third-party inspectionsRequired QualificationsEducational Background:• B.Sc• M.Sc• B.Pharm (Ayu)• M.Pharm (Ayu) (Preferred)Experience:• 1–2 years of experience in Quality Control within Ayurvedic or herbal manufacturingTechnical Skills:• Knowledge of herbal quality testing procedures• Familiarity with AYUSH and GMP compliance requirements• Experience in handling laboratory analytical instruments• Understanding of microbiological testing and stability studies• Knowledge of documentation practices and regulatory auditsSoft Skills:• Strong analytical and documentation skills• High attention to detail• Problem-solving ability• Team coordination and communication skillsCompany OverviewSunrise Remedies Pvt. Ltd. is a Gujarat-based pharmaceutical manufacturing company known for maintaining high-quality standards across conventional and Ayurvedic product segments. The company continues to expand its operations while adhering to strong regulatory and quality frameworks.FAQsQ1. Is Ayurvedic qualification mandatory?Ayurvedic qualification is preferred, but relevant QC experience in herbal manufacturing is essential.Q2. Is microbiological testing experience required?Yes, basic knowledge or exposure to microbiological testing is required.Q3. Are freshers eligible?No, 1–2 years of relevant QC experience is required.Q4. Does the role involve audit participation?Yes, the role includes supporting AYUSH and other regulatory audits.Q5. Is instrument handling experience necessary?Yes, experience with HPTLC, UV-Vis, and related instruments is expected.Application Tip• Highlight experience with herbal product testing• Mention instrument handling expertise clearly• Include exposure to AYUSH/GMP audits• Specify stability study and microbiology experience• Showcase documentation and CAPA handling experience

Why This Role MattersThe Quality Assurance Executive – Ayurvedic Division plays a critical role in ensuring that Ayurvedic and herbal products are manufactured, tested, and released in compliance with regulatory standards and Good Manufacturing Practices (GMP). This position safeguards product quality, safety, and consistency while maintaining adherence to traditional Ayurvedic principles and modern quality systems.By implementing quality policies, conducting audits, and driving continuous improvement initiatives, the role directly contributes to regulatory compliance and customer trust in herbal healthcare products.Job DescriptionSunrise Remedies Pvt. Ltd. is seeking a Quality Assurance Executive for its Ayurvedic division at the Santej, Ahmedabad facility. The selected candidate will oversee quality systems, ensure compliance with regulatory requirements, and coordinate cross-functional quality improvement initiatives within the manufacturing environment. The role requires hands-on knowledge of Ayurvedic product quality standards, documentation practices, auditing procedures, and GMP compliance.Key Features of the Role• Position: Quality Assurance Executive – Ayurvedic• Department: Quality Assurance – Ayurvedic• Location: Santej, Ahmedabad (Gujarat)• Experience Required: 1–2 years (Ayurvedic / Herbal QA)• Qualification: B.Pharm (Ayu) | M.Pharm (Ayu) (Preferred)• Industry: Ayurvedic / Herbal Pharmaceutical ManufacturingAdditional Benefits:• Transportation facility (as per company route coverage)• Mediclaim facility• Company-provided food facilityKey Responsibilities• Develop and implement quality assurance policies and procedures• Ensure compliance with industry standards and regulatory requirements• Conduct internal audits and quality assessments• Establish quality metrics and performance indicators• Collaborate with Production, QC, and other departments to maintain quality standards• Implement continuous improvement initiatives• Ensure adherence to GMP and regulatory compliance guidelines• Participate in inspections and audit readiness activities• Oversee product testing coordination in a manufacturing environment• Perform PM (Packaging Material), RM (Raw Material), and FG (Finished Goods) quality checksRequired QualificationsEducational Background:• B.Pharm (Ayurveda)• M.Pharm (Ayurveda) – PreferredExperience:• 1–2 years of experience in Quality Assurance within Ayurvedic or herbal manufacturingTechnical Skills:• Knowledge of QA systems and documentation• Understanding of GMP for Ayurvedic products• Experience in auditing and inspection processes• Familiarity with product testing procedures• Knowledge of PM, RM, and FG quality verificationSoft Skills:• Strong documentation and analytical skills• Attention to detail• Team coordination ability• Proactive approach toward quality improvementsCompany OverviewSunrise Remedies Pvt. Ltd. is a Gujarat-based pharmaceutical company committed to delivering high-quality healthcare products across various therapeutic segments, including Ayurvedic formulations. The company maintains strong quality systems and continues to expand its manufacturing capabilities while ensuring regulatory compliance and operational excellence.FAQsQ1. Is Ayurvedic qualification mandatory?Yes, B.Pharm (Ayu) or M.Pharm (Ayu) qualification is required.Q2. Is prior QA experience in herbal manufacturing necessary?Yes, 1–2 years of relevant experience is required.Q3. Are freshers eligible?No, prior QA exposure in Ayurvedic or herbal manufacturing is required.Q4. Is transportation available?Yes, transportation is provided based on company route coverage.Q5. Does the role involve audit participation?Yes, audit and inspection readiness is a key responsibility.Application Tip• Highlight Ayurvedic QA experience clearly• Mention GMP compliance exposure• Include audit and inspection experience• Specify knowledge of PM, RM, and FG quality checks• Showcase documentation and continuous improvement initiatives

Why This Role MattersThe Production Executive – Liquid Packing plays an important role in ensuring efficient, accurate, and GMP-compliant packaging operations within pharmaceutical manufacturing. This position directly impacts product quality, packaging integrity, and timely batch release by overseeing liquid filling and packing processes.By monitoring production lines, maintaining hygiene standards, and ensuring correct product volume and sealing integrity, the role contributes to regulatory compliance and customer safety. Maintaining production efficiency while minimizing downtime and waste is critical to overall operational excellence.Job DescriptionSunrise Remedies Pvt. Ltd. is hiring a Production Executive – Liquid Packing for its Santej, Ahmedabad facility. The selected candidate will be responsible for supervising liquid packing operations, maintaining GMP standards, and ensuring proper documentation of production activities.The role requires hands-on knowledge of filling, sealing, capping, and labeling machines, along with strong coordination with maintenance and quality teams to ensure uninterrupted operations.Key Features of the Role• Position: Production Executive – Liquid Packing• Department: Liquid Packing• Location: Santej, Ahmedabad (Gujarat)• Experience Required: 1–2 years (OSD background preferred)• Qualification: B.Sc | M.Sc | B.Pharm | M.Pharm (Preferred)• CTC: Up to ₹3 LPA• Industry: Pharmaceutical ManufacturingAdditional Benefits:• Transportation facility (as per company route coverage)• Mediclaim facility• Company-provided food facilityKey Responsibilities• Operate and monitor liquid filling, sealing, capping, and labeling machines• Ensure correct product volume and packaging specifications• Monitor production lines to minimize downtime and material waste• Inspect finished products for quality, leakage, and proper sealing• Maintain cleanliness and hygiene standards in the packing area• Follow Good Manufacturing Practices (GMP) and safety regulations• Record production data and maintain batch manufacturing records• Report machine faults and coordinate with maintenance teams• Ensure proper storage and handling of packaging materialsRequired QualificationsEducational Background:• B.Sc• M.Sc• B.Pharm• M.Pharm (Preferred)Experience:• 1–2 years of relevant production experience• Experience in OSD manufacturing preferredTechnical Skills:• Knowledge of liquid packing machinery operations• Understanding of GMP compliance• Familiarity with batch documentation practices• Awareness of safety and hygiene standardsSoft Skills:• Strong observation and monitoring skills• Attention to detail• Ability to work in a team-based manufacturing environment• Problem-solving ability in handling machine-related issuesCompany OverviewSunrise Remedies Pvt. Ltd. is a Gujarat-based pharmaceutical company known for its quality-driven manufacturing standards and commitment to healthcare excellence. The organization continues to expand its operations and offers career growth opportunities in production and quality functions.FAQsQ1. Is liquid packing experience mandatory?Yes, hands-on experience with liquid packing operations is required.Q2. Is OSD experience compulsory?OSD experience is preferred but not mandatory.Q3. Are freshers eligible?No, minimum 1 year of production experience is required.Q4. Is transportation provided?Yes, transportation is provided as per company route coverage.Q5. What is the salary range?CTC is up to ₹3 LPA depending on experience.Application Tip• Clearly mention experience with liquid filling and packing machines• Highlight GMP compliance exposure• Include production line monitoring experience• Specify batch record handling knowledge• Showcase coordination experience with maintenance teams

Why This Role MattersThe Senior Executive – Quality Control (QC) plays a vital role in ensuring pharmaceutical products meet defined quality standards before release. This position is responsible for maintaining analytical accuracy, regulatory compliance, and laboratory readiness in alignment with GMP requirements.By overseeing raw material, packaging material, and finished product analysis, the role directly contributes to product safety, regulatory compliance, and overall manufacturing excellence.Job DescriptionSunrise Remedies Pvt. Ltd. is seeking an experienced Senior QC Executive to join its Quality Control team at its Santej, Ahmedabad location.The selected candidate will be responsible for laboratory data review, analytical instrument handling (including HPLC), validation protocol review, audit preparedness, and cross-functional coordination with Production and QA teams.Key Features of the Role• Position: Senior Executive – Quality Control• Department: QC• Location: Santej, Ahmedabad (Gujarat)• Experience Required: 3–5 Years• Qualification: M.Sc | B.Pharm | M.Pharm (Preferred)• CTC: Up to ₹4.20 LPA• Industry: Pharmaceutical ManufacturingAdditional Benefits:• Transportation facility (as per company route coverage)• Mediclaim facility• Company-provided food facilityKey Responsibilities• Review analysis data for Raw Materials (RM), Packaging Materials (PM), and Finished Products (FP)• Verify calibration records and ensure compliance with standards• Review validation protocols and associated documentation• Handle and operate analytical instruments such as HPLC• Ensure adherence to quality standards in product analysis• Maintain cleanliness and discipline within the QC laboratory• Ensure audit readiness of QC lab and documentation• Maintain QC data and records on Pharmacloud• Coordinate with Production and QA teams for continuous quality improvementRequired QualificationsEducational Background:• M.Sc (Chemistry or relevant specialization)• B.Pharm• M.Pharm (Preferred)Experience:• 3–5 years of experience in pharmaceutical Quality ControlTechnical Skills:• Strong knowledge of HPLC operation and troubleshooting• Understanding of GMP documentation practices• Experience in validation protocol review• Knowledge of calibration and laboratory compliance standards• Familiarity with QC data management systems (e.g., Pharmacloud)Soft Skills:• Strong analytical and documentation skills• Detail-oriented approach• Team coordination ability• Audit readiness mindsetCompany OverviewSunrise Remedies Pvt. Ltd. is a Gujarat-based pharmaceutical manufacturing company known for its commitment to healthcare excellence and high-quality production standards. The company continues to expand its operations and offers structured growth opportunities within the pharmaceutical sector.FAQsQ1. Is HPLC experience mandatory?Yes, hands-on experience in handling HPLC instruments is required.Q2. Is M.Pharm compulsory?M.Pharm is preferred but not mandatory. M.Sc or B.Pharm candidates with relevant experience can apply.Q3. Is transportation provided?Yes, transportation is available based on company route coverage.Q4. Is this role open to freshers?No, minimum 3 years of QC experience in pharma is required.Q5. What type of products will be handled?Raw materials, packaging materials, and finished pharmaceutical products.Application Tip• Highlight HPLC experience clearly in your CV• Mention validation protocol review exposure• Include audit participation experience• Specify calibration documentation knowledge• Showcase GMP compliance experience

Why This Role MattersThe Contracts & Proposals Executive plays a key role in supporting global sales and project teams by developing accurate budgets and contract documents for clinical research projects. In the clinical research industry, well-structured contracts and clearly defined budgets are critical for project execution, financial transparency, and client satisfaction.This role ensures alignment between client requirements, operational feasibility, and commercial terms. By maintaining contract accuracy and database integrity, the position directly supports timely project initiation and revenue realization.At IQVIA, professionals in commercial and proposal functions contribute to accelerating clinical development by enabling seamless collaboration between sponsors and operational teams.Job DescriptionThe Contracts & Proposals Executive will be responsible for developing and preparing contracts and budgets for assigned customers to support the global sales team. The role involves close collaboration with project teams, internal stakeholders, and external clients to ensure proposals and agreements are aligned with customer needs and organizational standards. Under supervision, the candidate will prepare proposal documents, update contract databases, support negotiations, and ensure timely execution of new awards. The role requires strong coordination skills, attention to detail, and the ability to manage multiple deliverables within defined timelines.Key Features of the Role:• Position: Contracts & Proposals Executive• Industry: Clinical Research / Healthcare Intelligence• Qualification: Bachelor’s Degree (Life Science / Business Management or related field)• Focus Area: Budget preparation, contract development, proposal management• Client Interaction: Internal and external stakeholder coordination• Strong exposure to global sales support functions• Opportunity to work within a leading CRO environmentResponsibilities• Work closely with project teams to determine appropriate contract terms and conditions under supervision• Support preparation, review, and sign-off of budgets• Develop and prepare contract and proposal documents• Act as secondary customer interface on small projects• Support preparation, finalization, and distribution of budgets and contracts• Update and maintain proposal documents, contract databases, and tracking files• Prepare and update client-facing budget grids• Engage internal stakeholders to finalize budgets for work orders or change orders• Lead internal discussions to clarify customer requirements and resolve discrepancies• Ensure contracts align with client needs and master service agreements• Perform quality control checks on documents before distribution• Maintain accurate information in corporate databases and tracking reports• Act as primary interface for budget and proposal development on assigned projects• Develop execution plans for new award contracts to ensure timely completion• Perform additional duties as assigned by the managerRequired QualificationsCandidates should demonstrate strong communication, coordination, and analytical skills along with a structured approach to documentation and client interaction.Educational Requirements:• Bachelor’s Degree in Life Sciences, Business Management, or related field (Required)Experience and Skills:• Demonstrated project management skills• Ability to build and maintain strong customer relationships• Strong written and verbal communication skills• Good listening and negotiation abilities• Problem-solving and analytical skills• Attention to detail and document quality control expertise• Proficiency in Microsoft Office tools (Word, Excel, PowerPoint)• Ability to manage multiple deliverables under tight timelinesSalary InsightsCompensation will be aligned with industry standards for contracts and proposal professionals within the clinical research and CRO sector. Salary may vary based on prior experience in budget development, contract management, and client coordination.Company OverviewIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to life sciences and healthcare industries. The company supports pharmaceutical and biotechnology organizations in accelerating clinical development, improving commercialization strategies, and enhancing healthcare outcomes through data-driven solutions. With a strong global presence, IQVIA offers professionals opportunities to work in a collaborative, technology-driven, and growth-oriented environment.FAQsQ1. Is prior contract management experience required?While not mandatory, experience in proposals, budgets, or contract preparation is beneficial.Q2. Does this role involve client interaction?Yes, the role includes internal and external stakeholder coordination.Q3. Is this role technical or commercial?It is primarily a commercial and operational support role within clinical research.Q4. What tools are required for this role?Proficiency in Microsoft Office tools is required.Q5. Is project management experience important?Yes, demonstrated project management skills are highly valued.Application Tip• Highlight experience in budget preparation or contract documentation• Mention any exposure to CRO or clinical research environments• Showcase strong Excel and documentation skills• Demonstrate stakeholder coordination experience• Emphasize attention to detail and quality control abilities

Why This Role MattersSignal Management is a critical function within pharmacovigilance that ensures emerging safety information is proactively identified, assessed, and communicated. Effective signal detection and evaluation directly impact patient safety, product labeling, and overall benefit-risk assessment of medicinal products.At Amneal Pharmaceuticals, the Drug Safety Officer – Signal Management plays an essential role in safeguarding public health by ensuring compliance with global pharmacovigilance regulations and maintaining the integrity of safety surveillance systems. This role contributes to structured signal detection processes, regulatory reporting accuracy, and cross-functional pharmacovigilance enhancements.Job DescriptionWe are seeking a qualified and detail-oriented Drug Safety Officer to support Signal Management activities within the Pharmacovigilance function. The selected candidate will be responsible for identifying, analyzing, and evaluating potential safety signals arising from multiple data sources, and authoring structured safety documents in compliance with Standard Operating Procedures (SOPs) and regulatory guidelines.The role requires strong analytical skills, regulatory awareness, and the ability to synthesize complex safety data into clear and compliant documentation.Key Features of the Role• Exposure to global signal detection and signal evaluation processes• Involvement in benefit-risk assessment and labeling impact analysis• Opportunity to author Drug Safety Reports (DSRs)• Participation in cross-functional pharmacovigilance initiatives• Engagement in regulatory compliance and SOP development• Training and knowledge-sharing responsibilities within the PV teamResponsibilities• Prepare and maintain the Signal Schedule as per approved Standard Operating Procedures• Identify, analyze, and evaluate safety signals from various data sources• Assess risks that may result in labeling changes or updates to the product’s benefit-risk profile• Evaluate safety information and prepare product-specific ADR (Adverse Drug Reaction) Sheets• Author Drug Safety Reports (DSRs) for validated signals in compliance with SOPs• Communicate findings from routine and ad hoc signal detection activities to stakeholders• Contribute to cross-functional initiatives aimed at strengthening signal detection capabilities• Stay updated on new or revised regulatory requirements related to Signal Management• Ensure compliance with quality standards, regulatory timelines, and procedural consistency• Assist in preparation and revision of SOPs, work instructions, templates, and training materials• Deliver training sessions related to Signal Management activities as requiredRequired QualificationsEducational Requirements:• Pharm D. / Doctor of PharmacyExperience and Skills:• Experience in Pharmacovigilance with exposure to Signal Management activities preferred• Strong understanding of signal detection methodologies and benefit-risk assessment• Knowledge of global pharmacovigilance regulations and reporting requirements• Experience in authoring safety documents such as DSRs or ADR summaries• Strong analytical and critical thinking skills• Excellent written and verbal communication skills• High attention to detail and regulatory compliance awareness• Ability to work effectively in cross-functional environmentsSalary InsightsCompensation is aligned with industry standards for Pharmacovigilance professionals specializing in Signal Management. The final salary package depends on prior experience, technical expertise, and regulatory exposure. Industry-standard benefits, performance incentives, and professional development opportunities are typically included.Company OverviewAmneal Pharmaceuticals is a global pharmaceutical organization committed to delivering high-quality, affordable medicines. The company emphasizes regulatory compliance, operational excellence, and a culture of diversity and inclusion.The Human Resources team partners closely with business functions to support organizational effectiveness, compliance with employment regulations, talent development, and strategic workforce planning.FAQs• Is prior signal management experience mandatory?While not strictly mandatory, prior exposure to signal detection and evaluation processes is strongly preferred.• Does the role involve regulatory documentation?Yes, the role includes authoring Drug Safety Reports and preparing ADR documentation in line with regulatory standards.• Will training responsibilities be part of the job?Yes, candidates may be required to conduct training sessions related to Signal Management processes.• What type of regulatory knowledge is required?A strong understanding of global pharmacovigilance regulations and compliance requirements is essential.Application Tips• Highlight experience in signal detection, case processing, or aggregate reporting• Mention familiarity with global pharmacovigilance guidelines• Showcase documentation skills, especially safety report writing• Demonstrate examples of cross-functional collaboration• Emphasize compliance awareness and SOP adherence

Why This Role MattersAnalytical Development plays a critical role in ensuring the safety, efficacy, and quality of pharmaceutical products before they reach patients. In a regulated environment where precision and compliance are non-negotiable, robust analytical method development and validation form the backbone of successful product approvals and commercial manufacturing.At Corona Remedies Limited, this role directly supports product innovation across women’s healthcare, cardio-diabeto, pain management, urology, and other therapeutic segments. By developing and validating reliable analytical methods, the Analytical Development Scientist ensures regulatory compliance, smooth technology transfer, and consistent product quality throughout the lifecycle.Working at the Bhayla manufacturing facility in Gujarat provides exposure to a high-performance, cGMP-compliant environment focused on operational excellence and scientific rigor.Job DescriptionWe are seeking an experienced and detail-oriented Analytical Development Scientist to join the Analytical Development Lab (ADL) at the Bhayla Plant, Gujarat. The selected candidate will be responsible for developing, validating, and transferring analytical methods in line with ICH, cGMP, and GLP requirements.The role requires strong technical expertise in chromatographic and spectroscopic techniques, structured documentation practices, and cross-functional collaboration with Formulation R&D and Quality Control teams. The candidate must demonstrate strong analytical thinking, regulatory awareness, and problem-solving skills in a commercial pharmaceutical environment.Key Features of the Role• Hands-on exposure to analytical method development and validation• Work with advanced analytical instrumentation (HPLC, UPLC, GC, UV, FTIR)• Involvement in CTD/DMF documentation and regulatory submissions• Collaboration with R&D and QC for technology transfer• Opportunity to contribute to product scale-up and commercial manufacturing• Work in a cGMP-compliant manufacturing environmentResponsibilities• Develop, validate, and verify analytical methods for assay, dissolution, and related substances as per ICH guidelines• Operate analytical instruments including HPLC, UPLC, GC, UV, FTIR, and Dissolution Apparatus• Prepare and review analytical protocols, validation reports, and routine documentation• Generate Certificates of Analysis (COA) and support CTD/DMF compilation• Ensure compliance with cGMP and GLP documentation standards• Collaborate with Formulation R&D for method development during product development• Transfer validated analytical methods to Quality Control for scale-up and commercial production• Investigate and resolve analytical deviations, OOS, and OOT results• Maintain data integrity and adherence to regulatory standards• Participate in internal audits and regulatory inspections as requiredRequired QualificationsEducational Requirements:• M.Sc / M.Pharm / B.Pharm in relevant scientific disciplinesExperience and Skills:• 2 to 8 years of experience in Analytical Development within the pharmaceutical industry• Hands-on experience in method development and validation• Strong working knowledge of ICH guidelines and regulatory expectations• Practical exposure to chromatographic and spectroscopic instruments• Experience in a regulated manufacturing environment• Strong documentation, analytical reasoning, and problem-solving skills• Ability to work cross-functionally with R&D and QC teamsSalary InsightsThe compensation package is competitive and aligned with industry benchmarks for analytical development professionals in Gujarat. The expected salary range is approximately ₹4,00,000 to ₹12,00,000 per annum (CTC), depending on experience, technical proficiency, and regulatory exposure.Benefits typically include health insurance, performance incentives, structured career progression pathways, and opportunities for professional growth within a quality-driven pharmaceutical organization.Company OverviewCorona Remedies Limited is a leading pharmaceutical organization known for its focus on women’s healthcare, cardio-diabeto, pain management, and urology segments. The company operates advanced manufacturing facilities in Gujarat (including the Bhayla plant) and Himachal Pradesh.With a strong emphasis on cGMP compliance, innovation in formulations, and quality excellence, the organization continues to expand its capabilities in research, development, and commercial production.FAQs• Is prior ADL experience mandatory?Yes, relevant experience in analytical development within a pharmaceutical setup is required.• What type of products will I work on?Primarily pharmaceutical formulations across key therapeutic areas handled by the company.• Is regulatory documentation exposure important?Yes, familiarity with CTD/DMF documentation and compliance standards is highly preferred.• Where is the job located?Bhayla Plant, Gujarat.Application Tips• Highlight hands-on experience with HPLC, UPLC, and method validation projects• Emphasize regulatory compliance knowledge (ICH, cGMP, GLP)• Include examples of analytical issue resolution or method transfer experience• Demonstrate documentation accuracy and audit readiness• Showcase collaboration with R&D or QC teams

Why This Role MattersThe Senior Physiotherapist (MPT) at Physiocares – Rapid Recovery Team plays a crucial role in delivering high-quality patient-centered rehabilitation services. This position ensures effective treatment planning, smooth clinic operations, and compassionate care for patients in Nikol, Ahmedabad.Job DescriptionPhysiocares is hiring a Senior Physiotherapist with a minimum of 3 years of professional experience to manage patient consultations, develop treatment plans, and oversee daily clinic operations. This is a freelance / contractual role requiring independent clinic management and strong patient-handling skills.Key Features of the Role• Position: Senior Physiotherapist (MPT)• Company: Physiocares – Rapid Recovery Team• Location: Nikol, Ahmedabad, Gujarat• Employment Type: Freelance | Contractual / Temporary• Salary: ₹10,000 – ₹40,000 per month• Work Environment: Clinic-based (In-person)• Experience Required: Minimum 3 years• Eligibility: MPT preferredResponsibilities• Conduct detailed patient consultations and assessments• Develop accurate and personalized treatment plans• Provide compassionate and professional patient care• Manage OPD and maintain proper case records• Monitor patient progress and provide follow-up guidance• Oversee day-to-day clinic operations• Coordinate appointments, reports, and patient support activities• Maintain a positive, empathetic clinic environmentRequired Qualification• Master of Physiotherapy (MPT) preferred• (As mentioned in the job post: BHMS degree from a recognized institution)Educational Requirement• Relevant degree from a recognized institutionImportant Remarks• Minimum 3 years of professional experience required• Ability to independently manage clinic activities• Freelance engagement model• In-person roleExperience and Skills• Strong physiotherapy and rehabilitation knowledge• Good understanding of medical terminology and physiology• Excellent communication and patient-handling skills• Strong decision-making and problem-solving abilities• Professional, friendly, and empathetic attitude• Capability to manage clinic operations independentlySalary Insights• ₹10,000 – ₹40,000 per month• Salary may vary based on experience, patient load, and skill levelCompany OverviewPhysiocares – Rapid Recovery Team is a rehabilitation-focused clinic located in Nikol, Ahmedabad, Gujarat. The clinic emphasizes rapid recovery programs, compassionate care, and efficient clinic management to provide quality physiotherapy services.FAQsWho can apply?Candidates with relevant physiotherapy qualifications and minimum 3 years of experience.What is the salary range?₹10,000 – ₹40,000 per month.What type of job is this?Freelance / Contractual role.Is prior experience mandatory?Yes, minimum 3 years of professional experience is required.Where is the job located?Nikol, Ahmedabad, Gujarat.Application Tips• Highlight your 3+ years of clinical experience clearly at the top of your resume.• Mention your experience in OPD management and clinic operations.• Emphasize independent decision-making and patient care experience.• Clearly state your qualification (BPT/MPT) and current location.

Why This Role MattersThe Physiotherapist (MPT – Cardio) at Physiocares – Rapid Recovery Team plays a key role in delivering personalized physiotherapy care to patients with physical challenges. This position focuses on home-visit rehabilitation services, ensuring patients receive quality treatment and support in the comfort of their homes in the Bopal area of Ahmedabad.Job DescriptionPhysiocares – Rapid Recovery Team is urgently hiring a qualified MPT Physiotherapist for home-visit services. The role involves assessing patients, facilitating treatment and therapy sessions, and supporting rehabilitation plans. This is a full-time, in-person position suitable for candidates with 0–1 year of experience.Key Features of the Role• Position: Physiotherapist (MPT – Cardio)• Company: Physiocares – Rapid Recovery Team• Location: Nikol, Ahmedabad, Gujarat (Home Visit – Bopal Area)• Employment Type: Full-Time• Salary: Up to ₹20,000 per month• Work Environment: Home Visit (In-person)• Experience Required: 0–1 year• Eligibility: MPT requiredResponsibilities• Conduct patient assessments during home visits• Facilitate treatment and therapy sessions for physical rehabilitation• Develop and implement appropriate therapy plans• Build and maintain rapport with patients• Monitor patient progress and provide necessary guidance• Maintain proper documentation and administrative records• Coordinate with team members for effective patient careRequired Qualification• Master of Physiotherapy (MPT) – MandatoryEducational Requirement• MPT from a recognized institutionImportant Remarks• Home visit role (Bopal Area)• Suitable for freshers and candidates with up to 1 year of experience• Good physical fitness required• Immediate joining preferredExperience and Skills• Basic physiotherapy and rehabilitation knowledge• Strong interpersonal and communication skills• Ability to build patient rapport• Teamwork and coordination skills• Basic administrative and documentation skills• Patience, tolerance, and professional attitudeSalary Insights• Up to ₹20,000 per month• Salary may vary based on experience and performanceCompany OverviewPhysiocares – Rapid Recovery Team is a rehabilitation-focused clinic based in Nikol, Ahmedabad, Gujarat. The clinic provides physiotherapy services including home-visit care, focusing on rapid recovery programs and patient-centered rehabilitation support.FAQsWho can apply?Candidates with MPT qualification (0–1 year experience).What is the salary offered?Up to ₹20,000 per month.Is prior experience mandatory?No, freshers with MPT can apply.What type of job is this?Full-time, home-visit role.Where is the service area?Bopal Area, Ahmedabad (Clinic based in Nikol).Application Tips• Clearly mention your MPT qualification at the top of your resume.• Highlight any internship or clinical exposure during your studies.• Mention your willingness to perform home visits.• Include your current location and immediate availability.

Why This Role MattersThe IPQA Officer is a key position within the production floor that ensures all processes, products, and systems comply with stringent quality standards and regulatory requirements. By monitoring in-process activities, maintaining GMP practices, and ensuring cleanliness and hygiene, this role directly impacts product quality, operational efficiency, and customer satisfaction at HCP Wellness Private Limited.Job DescriptionHCP Wellness Private Limited is seeking a motivated IPQA Officer to join the In Process Quality Assurance (IPQA) department. The role involves overseeing day-to-day production quality activities, monitoring machines and processes, conducting audits, and ensuring compliance with standard operating procedures (SOPs) and regulatory guidelines. This position is ideal for freshers or candidates with limited experience in production quality assurance who are eager to grow in a GMP-compliant environment.Key Features of the Role• Monitor production floor activities for quality compliance daily• Train supervisors and production staff on quality procedures• Ensure contamination control by inspecting doors and controlled areas• Check and record air conditioning temperatures consistently• Monitor hygiene and cleaning standards across production areas• Verify proper utilization of floor space for smooth operations• Coordinate with Maintenance team to resolve infrastructure-related issues• Maintain records of rejected materials such as tubes, bottles, and other packaging components• Track machine breakdown time, running time, and operational parameters• Ensure all status labels and THM formats are updated regularly• Conduct line clearance and filling activity checks, including crimping and weight verification• Confirm proper cleaning of vessels and maintain documentation• Monitor finished goods quality control (FGQC) in the dispatch areaResponsibilities• Perform daily quality checks on production floor activities• Train production staff and supervisors on IPQA practices and SOP adherence• Inspect and maintain contamination-free production environments• Monitor and record temperature, cleanliness, and hygiene standards• Maintain proper documentation of rejected materials, vessel cleaning, and line clearance• Record operational parameters of machines, including downtime and running time• Conduct periodic checks on filling activities, crimping, and weights• Verify THM formats and update status labels consistently• Coordinate with QA/QC Manager for compliance and reporting• Support smooth production operations while ensuring quality standards are metRequired Qualifications• Diploma / B.Sc / B.Pharm / M.Pharm in Pharmacy, Life Sciences, Chemistry, or relevant fields• Freshers welcome; candidates with prior exposure to production or QA processes are preferred• Knowledge of GMP, hygiene standards, and basic quality monitoring practices• Strong attention to detail and adherence to SOPsEducational Requirements• Diploma / B.Sc / B.Pharm / M.Pharm in relevant fields• Training in GMP, hygiene, or quality practices is advantageousExperience and Skills• Freshers or 0–2 years of experience in pharmaceutical, personal care, or cosmetic production• Understanding of in-process quality checks and documentation• Ability to follow standard operating procedures (SOPs) and GMP guidelines• Strong observation and problem-solving skills• Teamwork and effective communication on the production floorSalary Insights• ₹15,000 – ₹20,000 per month, depending on qualifications and experience• Additional benefits include health insurance and provident fundCompany OverviewHCP Wellness Private Limited is a WHO-GMP certified manufacturer of personal care, cosmetic, and oral care products. The company emphasizes quality, innovation, and customer satisfaction. Employees are encouraged to collaborate, learn, and grow within a structured, GMP-compliant work environment.FAQsQ: Is prior experience required?Freshers are welcome. Any prior exposure to production or QA processes is beneficial.Q: Will training be provided?Yes, hands-on training on in-process quality assurance and GMP practices will be provided.Q: Are health and safety measures part of the role?Yes, adherence to GMP, hygiene standards, and safety protocols is mandatory.Application Tips• Highlight any experience or coursework related to quality assurance, GMP, or production monitoring• Emphasize attention to detail and ability to maintain accurate records• Showcase teamwork and communication skills for working on the production floor• Include relevant educational qualifications in Pharmacy, Life Sciences, or Chemistry

Why This Role MattersThe Tube Filling Operator plays a critical role in the production process of personal care and cosmetic products. Accurate and efficient tube filling ensures that products meet the company’s quality standards, maintain brand integrity, and satisfy customer expectations. By operating and monitoring filling equipment, this role contributes directly to production efficiency, product consistency, and overall operational excellence at HCP Wellness Private Limited.Job DescriptionHCP Wellness Private Limited is seeking motivated Tube Filling Operators to join its production team. The role involves operating automatic or semi-automatic tube filling machinery, monitoring production processes, and ensuring adherence to quality and safety standards. This hands-on position provides exposure to modern manufacturing equipment and techniques in a compliant and dynamic environment.Key Features of the Role• Operate and monitor automatic and semi-automatic tube filling machinery• Ensure consistent filling volumes, sealing quality, and product aesthetics• Set up, calibrate, and troubleshoot machinery as required• Maintain accurate production and batch documentation• Monitor production workflow and escalate issues as needed• Follow GMP and internal SOPs to maintain quality standards• Collaborate with QA and production teams to ensure seamless operationsResponsibilities• Operate tube filling equipment according to production schedules and SOPs• Inspect tubes for correct fill levels, sealing integrity, and visual appearance• Perform routine equipment maintenance, cleaning, and calibration• Record production data and maintain batch documentation for compliance purposes• Identify and report operational or quality deviations promptly• Support continuous improvement initiatives to enhance production efficiency• Ensure adherence to workplace safety standards and GMP requirementsRequired Qualifications• 0–3 years of experience in pharmaceutical, personal care, or cosmetic production (freshers may be considered)• Hands-on experience with tube filling or similar packaging machinery preferred• Knowledge of GMP, ISO standards, and basic production processes• Strong attention to detail and commitment to qualityEducational Requirements• Diploma / B.Sc / B.Pharm / M.Pharm in Pharmacy, Chemistry, Life Sciences, or relevant fields• ITI certifications in production or mechanical operations may be advantageousExperience and Skills• Familiarity with operating automatic or semi-automatic production machinery• Basic troubleshooting and calibration skills for filling equipment• Good documentation and record-keeping practices• Ability to work in a fast-paced production environment• Teamwork and communication skills for collaboration with production and QA teamsSalary Insights• Competitive salary based on experience and skill level• Opportunities for performance incentives and career growth within production and manufacturing functionsCompany OverviewHCP Wellness Private Limited is a WHO-GMP certified private label manufacturer specializing in personal care, cosmetics, and oral care products. Committed to quality, innovation, and customer satisfaction, the company serves global clients with customizable formulations. Employees are encouraged to grow, innovate, and contribute to a collaborative and high-performing work environment.FAQsQ: Do I need prior experience to apply?Freshers are welcome; prior experience in production or packaging machinery is advantageous.Q: Is training provided?Yes, hands-on training on tube filling machinery and production processes will be provided.Q: Are safety protocols part of the role?Absolutely. Following GMP and internal safety standards is essential.Application Tips• Highlight any hands-on experience with tube filling or packaging machinery• Emphasize familiarity with GMP, SOPs, and production documentation• Showcase attention to detail and ability to work in a production team• Mention any relevant educational qualifications or certifications in production, pharmacy, or life sciences

Why This Role MattersAnalytical Development plays a decisive role in ensuring pharmaceutical products meet regulatory, quality, and stability standards before reaching patients. Robust method development and validation directly support formulation innovation, regulatory submissions, and commercial manufacturing.At Corona Remedies Limited, the Analytical Development team supports product innovation across women’s healthcare, cardio-diabeto, pain management, and urology segments while maintaining strict cGMP and GLP compliance.Job DescriptionCorona Remedies Limited is expanding its Analytical Development Laboratory (ADL) team for its Gujarat manufacturing operations (including Bhayla plant). The role involves method development, validation, and transfer of analytical procedures for pharmaceutical formulations in a regulated environment.The selected candidate will collaborate closely with Formulation R&D and Quality Control teams to ensure accurate analytical support during development, scale-up, and commercial production stages.Key Features of the Role• Exposure to advanced analytical instrumentation• Involvement in method development and validation as per ICH guidelines• Participation in regulatory documentation (CTD/DMF support)• Cross-functional collaboration with R&D and QC• Opportunity to work in a growing formulation-focused organizationResponsibilities• Develop, validate, and verify analytical methods for assay, dissolution, and related substances• Operate instruments such as HPLC, UPLC, GC, UV, FTIR, and Dissolution Apparatus• Prepare and review analytical protocols and reports• Maintain COA, CTD, DMF, and related documentation• Ensure compliance with cGMP, GLP, and ICH guidelines• Support analytical method transfer to QC for commercial production• Investigate and resolve analytical deviations and issues• Perform stability sample analysis• Assist during audits and regulatory inspections• Ensure data integrity and proper documentation practicesRequired Qualifications• 2–8 years of experience in Analytical Development• Hands-on experience in method development and validation• Strong exposure to chromatographic techniques• Experience in regulated pharmaceutical environmentsEducational Requirements• M.Sc• Master of Pharmacy• Bachelor of PharmacyExperience and Skills• Strong knowledge of ICH guidelines• Expertise in HPLC/UPLC/GC method development• Experience in dissolution method optimization• Familiarity with regulatory documentation (CTD/DMF)• Good problem-solving and analytical skills• Strong documentation and compliance mindset• Ability to collaborate with cross-functional teamsSalary Insights• ₹4,00,000 to ₹12,00,000 per annum (CTC), depending on experience• Industry-standard benefits including health insurance and incentives• Growth opportunities within Analytical Development and Regulatory functionsCompany OverviewCorona Remedies Limited is a leading pharmaceutical company with a strong presence in women’s healthcare, cardio-diabeto, pain management, and urology segments. With advanced manufacturing facilities in Gujarat and Himachal Pradesh, the company emphasizes innovation, regulatory compliance, and high-quality formulation development.FAQsQ: Is method development experience mandatory?Yes, hands-on experience in method development and validation is preferred.Q: Will the role involve regulatory documentation?Yes, preparation and review of CTD/DMF-related analytical documents are part of the responsibility.Q: Is experience in a regulated environment required?Yes, exposure to cGMP/GLP-regulated setups is important.Application Tips• Mention instruments handled and methods developed• Highlight experience with ICH-compliant validation• Include exposure to CTD/DMF documentation• Quantify number of methods validated or transferred

Why This Role MattersPackaging and labeling are critical final steps in pharmaceutical manufacturing. Proper packaging ensures product protection, accurate labeling guarantees regulatory compliance, and efficient dispatch supports market availability. Errors at this stage can impact both patient safety and brand reputation.At Forever Lifescience Pvt. Ltd., the Packing Department plays a key role in ensuring that antifungal creams, ointments, gels, and other dermatological products are packed accurately and dispatched efficiently while maintaining WHO-GMP standards.Job DescriptionForever Lifescience Pvt. Ltd. is hiring for its Packing Department at Moraiya, Ahmedabad. The role involves handling packaging line operations, labeling activities, and coordinating dispatch processes to meet production targets and quality norms.Freshers and candidates with up to 3 years of experience in pharmaceutical or skincare manufacturing are encouraged to apply. This position offers hands-on exposure to packaging operations in a regulated manufacturing environment.Key Features of the Role• Opportunity for freshers and early-career professionals• Exposure to pharmaceutical packaging operations• Work in a WHO-GMP certified facility• Career growth in manufacturing and supply operations• Involvement in expanding production setupResponsibilities• Operate and monitor packaging machinery• Perform labeling activities as per approved artwork• Ensure line clearance before and after batch operations• Maintain packaging batch records and documentation• Coordinate with QA for in-process checks• Ensure compliance with GMP and safety standards• Support dispatch and material handling activities• Maintain cleanliness and 5S practices in packing area• Report deviations or discrepancies during packaging• Work in shifts as per production schedulesRequired Qualifications• Freshers or 0–3 years of experience in pharmaceutical/skincare packing• Basic understanding of GMP practices• Willingness to work in shifts• Strong attention to detail and teamwork skillsEducational Requirements• B.Sc• B.Pharm• M.PharmExperience and Skills• Basic knowledge of packaging line operations• Understanding of labeling compliance• Familiarity with documentation and batch record practices• Good communication skills• Ability to follow SOPs and safety guidelines• Commitment to quality and production targetsSalary Insights• Competitive CTC (no bar for the right candidate)• Learning and career growth opportunities• Exposure to regulated pharmaceutical packaging• Stable career path in manufacturing operationsCompany OverviewForever Lifescience Pvt. Ltd. is a WHO-GMP certified pharmaceutical manufacturer specializing in dermatological and external preparation products. With a modern facility in Moraiya, Ahmedabad, the company is expanding operations to support growing demand in skincare formulations.FAQsQ: Are freshers eligible?Yes, freshers are welcome to apply.Q: Is prior packing experience mandatory?Not mandatory, but preferred for experienced candidates.Q: Will shift work be required?Yes, based on production schedules.Application Tips• Mention packaging machines or lines handled (if any)• Highlight GMP knowledge and documentation exposure• Include internship or training experience (for freshers)• Emphasize attention to detail and shift flexibility

Why This Role MattersQuality Assurance ensures that pharmaceutical products are manufactured, tested, and released in full compliance with regulatory and GMP standards. In dermatological and external preparations, strong QA systems are essential to maintain product safety, documentation accuracy, and audit readiness.At Forever Lifescience Pvt. Ltd., the QA team safeguards quality systems and supports the company’s expansion in antifungal creams, ointments, gels, and other skincare formulations.Job DescriptionForever Lifescience Pvt. Ltd. is hiring for its Quality Assurance Department at Moraiya, Ahmedabad. The role focuses on ensuring regulatory compliance, documentation control, audit coordination, and adherence to quality systems across manufacturing operations.Freshers and candidates with up to 3 years of pharmaceutical experience are encouraged to apply. This position offers exposure to QA systems in a WHO-GMP certified manufacturing environment.Key Features of the Role• Opportunity for freshers and early-career professionals• Exposure to GMP documentation and audit processes• Work in a WHO-GMP certified facility• Career growth in Quality Assurance functions• Involvement in expanding pharmaceutical operationsResponsibilities• Review and maintain GMP documentation and SOPs• Perform line clearance and in-process QA checks• Support batch record review and approval processes• Assist in handling deviations, CAPA, and change controls• Participate in internal audits and regulatory inspections• Ensure compliance with WHO-GMP standards• Maintain document control systems• Coordinate with Production and QC teams• Support training activities related to GMP compliance• Follow shift schedules as requiredRequired Qualifications• Freshers or 0–3 years of experience in pharmaceutical QA• Basic knowledge of GMP and quality systems• Willingness to work in shifts• Strong documentation and attention to detailEducational Requirements• B.Sc• B.Pharm• M.PharmExperience and Skills• Understanding of GMP documentation practices• Knowledge of deviation and CAPA concepts• Good communication and teamwork skills• Strong analytical and compliance mindset• Ability to follow SOPs and regulatory guidelines• Commitment to quality and data integritySalary Insights• Competitive CTC (no bar for deserving candidates)• Learning and development opportunities• Exposure to audit and compliance processes• Growth prospects within Quality AssuranceCompany OverviewForever Lifescience Pvt. Ltd. is a WHO-GMP certified pharmaceutical manufacturer specializing in dermatological and external preparation products. Operating from Moraiya, Ahmedabad, the company is expanding its production and quality operations to meet growing market demand.FAQsQ: Are freshers eligible?Yes, freshers with relevant educational background are welcome.Q: Is prior QA experience mandatory?Not mandatory, but preferred for experienced candidates.Q: Will the role involve audits?Yes, support during internal and external audits is part of the role.Application Tips• Highlight GMP and documentation knowledge• Mention any internship or industrial training experience• Include exposure to audits or deviation handling (if any)• Emphasize attention to detail and compliance focus

Why This Role MattersQuality Control is the backbone of pharmaceutical manufacturing. In dermatological and external preparations, rigorous testing of raw materials, in-process samples, and finished products ensures purity, safety, stability, and therapeutic effectiveness.At Forever Lifescience Pvt. Ltd., the QC team plays a critical role in maintaining WHO-GMP standards while supporting the company’s expansion in antifungal creams, ointments, gels, and other skincare formulations.Job DescriptionForever Lifescience Pvt. Ltd. is hiring for its Quality Control Department at Moraiya, Ahmedabad. The role involves testing raw materials, monitoring in-process samples, and analyzing finished dermatological products to ensure compliance with quality specifications and regulatory standards.Freshers as well as candidates with up to 3 years of pharmaceutical experience are encouraged to apply. The position offers hands-on exposure to QC operations in a GMP-compliant manufacturing environment.Key Features of the Role• Opportunity for freshers and early-career professionals• Exposure to analytical testing in dermatology manufacturing• Work in a WHO-GMP certified facility• Career growth in Quality Control operations• Involvement in expanding production environmentResponsibilities• Test raw materials, packaging materials, and finished products• Perform in-process quality checks during manufacturing• Conduct routine analytical testing as per specifications• Maintain laboratory documentation and records• Ensure compliance with GMP and safety guidelines• Support stability studies and sample analysis• Report out-of-specification (OOS) results• Maintain laboratory instruments and calibration records• Coordinate with Production and QA teams• Follow SOPs and shift schedules as requiredRequired Qualifications• Freshers or 0–3 years of experience in pharmaceutical QC• Basic understanding of GMP practices• Willingness to work in shifts• Strong attention to detail and analytical mindsetEducational Requirements• B.Sc (Science stream)• B.Pharm• M.PharmExperience and Skills• Basic knowledge of analytical testing techniques• Familiarity with laboratory documentation practices• Good communication and teamwork skills• Understanding of quality standards and compliance• Ability to follow SOPs and testing protocols• Commitment to accuracy and data integritySalary Insights• Competitive CTC (no bar for deserving candidates)• Learning and development opportunities• Exposure to regulated skincare manufacturing• Growth prospects in Quality Control functionsCompany OverviewForever Lifescience Pvt. Ltd. is a WHO-GMP certified pharmaceutical manufacturer specializing in high-quality dermatological and external preparation products. With a modern facility in Moraiya, Ahmedabad, the company is expanding operations to support growing demand in skincare formulations.FAQsQ: Are freshers eligible for this role?Yes, freshers with relevant educational background can apply.Q: Is prior QC experience mandatory?Not mandatory, but preferred for experienced candidates.Q: Will shift work be required?Yes, depending on production and laboratory schedules.Application Tips• Mention laboratory instruments handled (if any)• Highlight GMP knowledge and documentation exposure• Include internship or training experience (for freshers)• Emphasize accuracy and attention to detail

Why This Role MattersExternal preparations such as antifungal creams, ointments, and gels require precision in formulation, homogenization, filling, and packaging to ensure product stability, safety, and therapeutic effectiveness. Production teams are the backbone of consistent quality and compliance in dermatological manufacturing.At Forever Lifescience Pvt. Ltd., this role supports the company’s expansion in high-quality skincare and external preparations, contributing directly to efficient production operations at its Moraiya, Ahmedabad facility.Job DescriptionForever Lifescience Pvt. Ltd., a WHO-GMP certified pharmaceutical manufacturer, is hiring for its Production Department at Moraiya, Ahmedabad. The role involves operating manufacturing equipment, handling formulation processes, and ensuring smooth production of creams, ointments, gels, and other dermatological products.Both freshers and candidates with up to 3 years of experience are encouraged to apply. Selected candidates will gain hands-on exposure to external preparation manufacturing in a regulated environment.Key Features of the Role• Opportunity for freshers and early-career professionals• Hands-on exposure to cream and ointment manufacturing• Work in a WHO-GMP certified facility• Career growth in dermatology-focused pharma manufacturing• Involvement in a fast-growing production setupResponsibilities• Operate manufacturing and mixing equipment for creams, ointments, and gels• Assist in formulation and batch processing activities• Monitor production parameters and record batch data• Ensure adherence to GMP and safety guidelines• Maintain cleanliness and hygiene standards in production areas• Perform line clearance and equipment checks• Coordinate with QA/QC teams for in-process approvals• Support documentation and batch record maintenance• Troubleshoot minor operational issues• Follow shift schedules as assignedRequired Qualifications• Freshers or 0–3 years of experience in pharmaceutical/skincare manufacturing• Basic knowledge of GMP practices• Willingness to work in shifts• Strong attention to detail and teamwork skillsEducational Requirements• B.Sc• B.Pharm• M.Pharm Experience and Skills• Understanding of cream/ointment manufacturing processes (preferred)• Basic knowledge of pharmaceutical documentation• Good communication skills• Ability to follow SOPs and safety protocols• Commitment to quality and compliance• Adaptability in a growing manufacturing environmentSalary Insights• Competitive CTC (no bar for the right candidate)• Learning and development opportunities• Exposure to large-scale dermatological manufacturing• Growth prospects within expanding production operationsCompany OverviewForever Lifescience Pvt. Ltd. is a WHO-GMP certified pharmaceutical manufacturer specializing in high-quality skincare and dermatological formulations, including antifungal creams, ointments, and gels. The company operates a modern production facility in Moraiya, Ahmedabad, and is currently expanding operations to meet increasing market demand.FAQsQ: Are freshers eligible to apply?Yes, freshers are welcome.Q: Is prior skincare manufacturing experience mandatory?Not mandatory, but preferred for experienced candidates.Q: Will shift work be required?Yes, depending on production schedules.Application Tips• Mention any hands-on experience with cream/ointment manufacturing• Highlight GMP knowledge and documentation exposure• Include internship or industrial training details (for freshers)• Emphasize willingness to work in shifts and relocate to Moraiya

Why This Role MattersIn botanical and herbal manufacturing, maintaining contamination-free production and regulatory compliance is essential for ensuring product safety and market credibility. This role plays a crucial part in strengthening the Quality Management System (QMS), ensuring vendor reliability, and maintaining documentation accuracy across operations.As a Quality Assurance Executive, you will directly contribute to maintaining GMP compliance, supporting audits, and ensuring that products meet the highest quality standards required in pharmaceutical, nutraceutical, and cosmetic markets. This is an excellent opportunity for early-career QA professionals to grow in a regulated and expanding manufacturing environment.Job DescriptionPhyto Life Sciences Pvt. Ltd. is seeking a Quality Assurance Executive to join its manufacturing facility in Santej, Gujarat. The selected candidate will be responsible for supporting Quality Management System activities, vendor qualification processes, regulatory compliance, and documentation control.This role is ideal for candidates with 1 to 4 years of experience in pharmaceutical, herbal, ayurvedic, nutraceutical, or life sciences industries who are detail-oriented and compliance-focused.Key Features of the Role• Opportunity to work in botanical and herbal product manufacturing• Exposure to pharmaceutical and nutraceutical quality systems• Involvement in vendor qualification and compliance processes• Hands-on experience with QMS and documentation management• Participation in audits and regulatory inspections• Career growth within a contamination-controlled manufacturing environmentResponsibilities• Perform vendor qualification and vendor assessment activities• Maintain and manage Quality Management System documentation• Handle SOP preparation, review, and control processes• Ensure accurate record-keeping and documentation integrity• Support internal and external audits and inspections• Assist in deviation handling and CAPA implementation• Ensure compliance with GMP and internal quality protocols• Coordinate with cross-functional teams to maintain quality standards• Monitor adherence to regulatory guidelines and company policiesRequired Qualifications• 1 to 4 years of experience in Quality Assurance• Experience in pharmaceutical, herbal, ayurvedic, nutraceutical, or life sciences sectors preferred• Working knowledge of GMP and regulatory compliance• Understanding of documentation control and QMS processes• Immediate availability to joinEducational Requirements• B.Pharm, M.Pharm, BSc/MSc in Chemistry, Microbiology, Life Sciences, or related field (preferred)• Additional certifications in GMP or Quality Systems are advantageousExperience and Skills• Strong attention to detail and documentation accuracy• Analytical and problem-solving abilities• Basic understanding of regulatory requirements• Ability to work effectively within a team• Good written and verbal communication skills• Organized and compliance-focused mindsetSalary Insights• Expected salary range: ₹3.5–6.5 LPA depending on experience and negotiation• Performance-based incentives (as per company policy)• Health insurance benefits• Professional development opportunities• Standard industry benefits as applicableCompany OverviewPhyto Life Sciences Pvt. Ltd. specializes in high-quality botanical and herbal products serving pharmaceutical, nutraceutical, and cosmetic markets. With manufacturing facilities in Gujarat, including Santej, the company emphasizes contamination-free production processes and advanced extraction techniques.The organization is focused on maintaining strong regulatory compliance and quality systems to support domestic and international markets.FAQsQ: Is herbal industry experience mandatory?A: Not mandatory, but experience in pharmaceutical or regulated manufacturing environments is preferred.Q: Will this role involve audit participation?A: Yes, candidates will support internal and external audits.Q: Is immediate joining compulsory?A: Immediate availability is highly preferred for this role.Q: What kind of QMS exposure is expected?A: Documentation control, SOP management, vendor qualification, and compliance monitoring.Application Tips• Highlight vendor qualification or audit experience clearly• Mention GMP and QMS knowledge in your CV• Quantify documentation handling or compliance contributions• Demonstrate attention to detail and regulatory understanding• Keep your resume structured and compliance-focused

Why This Role MattersIn the pharmaceutical industry, regulatory approval is the gateway to market access. Without a well-prepared, technically accurate, and guideline-compliant dossier, even the most effective formulation cannot reach patients. The Regulatory Affairs Executive plays a central role in compiling and reviewing regulatory submissions in alignment with international standards such as the Common Technical Document (CTD) and ASEAN Common Technical Dossier (ACTD) formats.This role directly supports global product registrations across ROW (Rest of World), LATAM, and African markets. Each region has unique regulatory expectations, documentation standards, and technical review procedures. A well-prepared dossier ensures faster approvals, reduced queries, and successful product launches.By preparing high-quality technical documents, validating analytical data in line with International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use guidelines, and responding to regulatory authority queries, this position contributes significantly to the company’s international expansion and regulatory credibility.Job DescriptionThe Regulatory Affairs Executive is responsible for preparation, compilation, review, and submission of pharmaceutical dossiers as per CTD/ACTD formats and country-specific requirements. The role involves coordination with manufacturing, quality assurance, analytical development, and R&D teams to gather technical data for regulatory submissions.The candidate will handle documentation for multiple dosage forms including oral solids, liquids, injectables, ophthalmic, and topical formulations. Additionally, this role involves responding to regulatory authority queries, reviewing Drug Master Files (DMFs), and supporting product development documentation aligned with global regulatory standards.The position requires strong technical writing skills, attention to detail, regulatory knowledge, and the ability to manage multiple submissions simultaneously.Key Features of the Role• Preparation of CTD and ACTD dossiers for global markets• Exposure to ROW, LATAM, and African regulatory frameworks• Handling diverse dosage forms• Interaction with cross-functional technical teams• Direct involvement in regulatory query managementResponsibilities• Prepare and compile dossiers in CTD and ACTD formats (Modules I, II, III, IV, and V) as per country-specific regulatory requirements.• Draft and review technical documents including raw material specifications and finished product specifications.• Document manufacturing processes and product development reports.• Compile and review stability study reports and process validation documents.• Review analytical method validation documents in compliance with ICH guidelines.• Conduct Drug Master File (DMF) review to ensure completeness and regulatory compliance.• Prepare and submit Product Dossiers (PD) for product registration in international markets.• Respond to technical queries raised by regulatory authorities.• Coordinate with Quality Assurance, R&D, Production, and Analytical teams for data collection.• Ensure accuracy, consistency, and completeness of regulatory submissions.• Maintain regulatory documentation archives and version control systems.• Monitor updates in global regulatory requirements and adapt documentation accordingly.Dosage Forms Handled• Oral Solid Dosage Forms (Tablets, Capsules)• Liquid Formulations• Injectable Products• Ophthalmic Preparations• Topical Dosage FormsMarket Exposure• ROW (Rest of World) Markets• Latin American (LATAM) Countries• African Regulatory MarketsRequired Qualifications• Bachelor’s degree in Pharmacy (B.Pharm) or Master’s degree in Pharmacy (M.Pharm).• 1–5 years of experience in pharmaceutical regulatory affairs or dossier preparation.• Strong understanding of CTD and ACTD formats.• Knowledge of ICH guidelines for analytical validation and stability studies.Educational Requirements• B.Pharm / M.Pharm (Regulatory Affairs, Pharmaceutics, Pharmaceutical Analysis preferred).• Additional training in international regulatory documentation is advantageous.Experience and Skills• Hands-on experience in dossier preparation for international markets.• Strong knowledge of CTD Modules I–V.• Familiarity with ACTD requirements for ASEAN and other regions.• Experience reviewing analytical method validation reports.• Understanding of stability study requirements and process validation documentation.• Ability to draft high-quality technical responses to regulatory authority queries.• Strong documentation and technical writing skills.• Excellent coordination skills for cross-functional collaboration.• Ability to handle multiple submissions with strict deadlines.• High level of accuracy and attention to detail.Salary InsightsThe offered salary range of ₹18,000 to ₹60,000 per month depends on:• Years of regulatory experience• Exposure to global markets (LATAM, Africa, ROW)• Technical expertise in CTD/ACTD preparation• Experience handling regulatory queries independentlyIn addition to base salary, the company provides Provident Fund benefits as per statutory requirements.Company OverviewThe organization operates within the pharmaceutical manufacturing and export sector, focusing on regulatory-compliant product registration across international markets. With a growing footprint in LATAM, African, and ROW markets, the company emphasizes technical excellence and adherence to global regulatory standards.The regulatory affairs team plays a crucial role in ensuring that all submissions meet international guidelines and local regulatory authority expectations. Through accurate documentation and efficient query resolution, the team supports timely product approvals and global business expansion.FAQsWhat formats will the candidate work with?CTD and ACTD formats covering Modules I to V.Is experience in multiple dosage forms required?Yes, experience handling oral, liquid, injectable, ophthalmic, and topical dosage forms is preferred.Does the role involve query response handling?Yes, preparing and submitting technical responses to regulatory authorities is a key responsibility.Which markets will be handled?ROW, LATAM, and African countries.Is ICH knowledge mandatory?Yes, knowledge of ICH guidelines for method validation and stability studies is essential.Application Tips• Highlight direct experience with CTD/ACTD dossier preparation.• Mention specific markets handled (LATAM, Africa, ROW).• Provide examples of technical query responses you have prepared.• Emphasize experience with stability data and process validation documentation.• Showcase strong documentation and regulatory coordination skills.