Pharmacy Jobs

Why This Role MattersThis Locum Clinical Pharmacist role provides a unique opportunity to support hospital-based patient care while gaining valuable clinical experience. It plays a critical role in ensuring safe medication use, supporting multidisciplinary teams, and improving patient outcomes in a hospital setting.Job DescriptionAussie Locums is hiring Locum Clinical Pharmacists for hospital roles in Tasmania. This opportunity is open to both clinical and community pharmacists, offering hands-on hospital experience with full travel and accommodation support.Key Features of the Role:• Open to both clinical and community pharmacists• Opportunity to gain hospital pharmacy experience• Flexible contract duration (8 / 12 / 26 weeks)• Travel and accommodation fully covered• Competitive locum hourly rates• Work in a scenic and highly desirable locationResponsibilities• Provide clinical pharmacy services in hospital settings• Support medication dispensing and ward-based activities• Assist in patient medication management and counseling• Collaborate with healthcare teams for optimal patient outcomes• Follow hospital protocols and quality standards• Support inpatient, outpatient, and day-care services• Work under guidance of senior pharmacists when requiredRequired QualificationsEducational Requirements:• Bachelor of Pharmacy or equivalentExperience and Skills:• AHPRA registration (mandatory)• Clinical or community pharmacy experience• Strong communication and teamwork skills• Ability to adapt to hospital pharmacy environment• Positive attitude and professional competence• Ability to complete credentialing requirements promptly• Hospital experience (desirable but not mandatory)• Valid working rights in AustraliaSalary Insights• Hourly Rate: $70 – $85 per hour (depending on experience)• Additional Benefits:• Superannuation• Travel (return) fully covered• Accommodation provided• No out-of-pocket expensesCompany OverviewAussie Locums specializes in placing healthcare professionals across Australia. The organization offers flexible locum opportunities with strong support, helping professionals gain diverse clinical exposure across healthcare settings.FAQs• Can community pharmacists apply?Yes, community pharmacists are encouraged to apply for hospital exposure.• What is the contract duration?Flexible – 8, 12, or 26 weeks.• Is travel and accommodation included?Yes, fully covered with no personal expense.• What is the salary range?$70 to $85 per hour plus superannuation.• What registration is required?AHPRA registration is mandatory.Application Tips• Ensure AHPRA registration is active• Prepare credentialing documents in advance• Highlight any clinical or hospital exposure• Be flexible with travel and contract duration• Apply early for preferred dates and locations

Why This Role MattersThe Pharmacist in Charge is a key leadership position responsible for ensuring safe pharmacy operations, delivering high-quality patient care, and driving community health outcomes. This role is critical in maintaining compliance, mentoring teams, and enhancing patient trust in community pharmacy services.Job DescriptionScaffidi Group is hiring a full-time Pharmacist in Charge for Priceline Pharmacy Port Pirie. This role involves overseeing pharmacy operations, delivering professional healthcare services, and leading a customer-focused pharmacy team.Key Features of the Role:• Full-time leadership opportunity in a growing pharmacy group• Suitable for both experienced and newly registered pharmacists• Relocation assistance provided• Strong career growth and development opportunities• Supportive environment with guidance from senior leadership• Exposure to regional community healthcareResponsibilities• Oversee daily pharmacy operations and ensure smooth workflow• Dispense medications accurately and ensure patient safety• Provide expert clinical advice and healthcare services• Maintain compliance with regulatory and professional standards• Build strong relationships with customers and the local community• Lead and support pharmacy staff to ensure high performance• Promote a culture of teamwork and patient-centered careRequired QualificationsEducational Requirements:• Bachelor of PharmacyExperience and Skills:• Current AHPRA registration (mandatory)• Strong communication and interpersonal skills• Leadership ability and team management skills• Customer-focused approach to patient care• Ability to manage pharmacy operations efficiently• Valid working rights in AustraliaSalary Insights• Competitive hourly rate (based on experience)• Additional benefits include relocation assistance, training, and career developmentCompany OverviewScaffidi Group is a rapidly expanding pharmacy network across Australia. Through brands like Priceline Pharmacy, the group delivers high-quality healthcare and retail services, focusing on innovation, patient care, and community engagement.FAQs• Is this role suitable for freshers?Yes, newly registered pharmacists are encouraged to apply.• What is the job location?Port Pirie, South Australia.• Is relocation support available?Yes, relocation assistance is provided.• What registration is required?AHPRA registration is mandatory.• What type of role is this?Full-time Pharmacist in Charge position.Application Tips• Highlight leadership or team management experience• Ensure your AHPRA registration is active• Emphasize customer service and patient care skills• Be prepared for scenario-based and operational questions• Apply early to secure this opportunity

Why This Role MattersPharmacists in community settings play a crucial role in improving public health by ensuring safe medication use, providing clinical advice, and supporting preventive healthcare services. This role directly impacts patient well-being by delivering accessible and trusted healthcare within the community.Job DescriptionStar Pharmacy Group is hiring Pharmacists for part-time or casual roles within its Star Discount Chemist network in the Eastern Suburbs. The role focuses on delivering patient-centered pharmacy services, medication management, and clinical support in a community pharmacy setting.Key Features of the Role:• Flexible part-time or casual working hours (up to 30 hours/week)• Opportunity to work in a community-focused pharmacy environment• Access to ongoing training, mentoring, and development programs• Employee benefits including discounts and wellbeing initiatives• Clear career progression within a large pharmacy networkResponsibilities• Dispense medications accurately and efficiently• Provide patient counseling and clinical advice• Deliver healthcare services such as vaccinations and medication reviews• Conduct basic health checks and patient assessments• Collaborate with pharmacists, assistants, and healthcare teams• Maintain compliance with pharmacy regulations and standards• Build strong relationships with patients and the local communityRequired QualificationsEducational Requirements:• Bachelor of PharmacyExperience and Skills:• Current AHPRA registration (mandatory)• Strong communication and interpersonal skills• Attention to detail and accuracy in dispensing• Customer-focused approach to patient care• Vaccination accreditation (preferred)• First Aid and CPR certification (preferred)• Ability to work weekends and evening shiftsSalary Insights• Competitive pay based on experience• Additional benefits include staff discounts, wellbeing programs, and career development opportunitiesCompany OverviewStar Pharmacy Group has been serving communities since 2003, operating over 65 pharmacies across Australia. Through brands like Star Discount Chemist and Priceline, the group focuses on delivering accessible healthcare and improving community well-being.FAQs• What type of role is offered?Part-time or casual (up to 30 hours per week).• What registration is required?AHPRA registration is mandatory.• Are additional certifications required?Vaccination accreditation is preferred; First Aid/CPR is an advantage.• What is the work schedule?Includes weekends and Thursday nights.• What benefits are provided?Competitive salary, staff discounts, training, and career growth opportunities.Application Tips• Ensure your AHPRA registration is active• Highlight experience in community pharmacy and patient counseling• Mention certifications like vaccination, First Aid, and CPR• Demonstrate strong communication and customer service skills• Apply early to secure your opportunity

Why This Role MattersThe Clinical Research Coordinator (CRC) plays a vital role in ensuring the successful execution of clinical trials. This position bridges investigators, patients, and sponsors, ensuring studies are conducted ethically, efficiently, and in compliance with regulatory standards. It directly contributes to advancing healthcare innovation and evidence-based medicine.Job DescriptionMetta Clinical is hiring a Clinical Research Coordinator (CRC) for its Raipur location. The role involves managing clinical trial operations, coordinating with investigators, and ensuring accurate documentation and compliance with ICH-GCP guidelines.Key Features of the Role:• Opportunity to work in live clinical trial environments• Hands-on experience in trial coordination and site management• Exposure to regulatory documentation and audits• Career growth in Clinical Research, CRA, CDM, and Pharmacovigilance• Work closely with investigators and healthcare professionalsResponsibilities• Coordinate clinical trials as per protocol and regulatory guidelines• Assist investigators in study initiation, execution, and closure• Maintain accurate documentation (ICF, CRF, source data)• Manage patient recruitment, screening, and follow-ups• Ensure compliance with ICH-GCP, SOPs, and regulatory standards• Handle monitoring visits and ensure audit readiness• Collect, verify, and report clinical data accurately• Coordinate with cross-functional teams and stakeholdersRequired QualificationsEducational Requirements:• B.Pharm or Science Graduate (Life Sciences preferred)Experience and Skills:• 1–2 years of experience in clinical trials• Strong understanding of ICH-GCP guidelines• Knowledge of clinical trial processes and documentation• Good communication and coordination skills• Ability to manage multiple tasks in a fast-paced environment• Preference for candidates based in or near RaipurSalary Insights• Estimated Salary: ₹2.4 LPA – ₹4.0 LPA• Additional benefits include learning exposure and career growth opportunitiesCompany OverviewMetta Clinical is a clinical research organization focused on delivering high-quality clinical trial services. The company works closely with investigators and healthcare institutions to support research that improves patient outcomes and advances medical science.FAQs• What is the job location?Raipur, Chhattisgarh (On-site role)• What experience is required?1–2 years in clinical trials• What qualifications are needed?B.Pharm or Life Sciences graduate• What is the salary range?₹2.4 LPA – ₹4.0 LPA• What is the last date to apply?01 April 2026Application Tips• Highlight clinical trial experience and GCP knowledge in your resume• Mention hands-on experience with CRFs, ICFs, and patient handling• Prepare for questions on trial processes and regulatory guidelines• Keep all documents ready (certificates, ID proof)• Apply before the deadline to secure your opportunityImportant Date• Application Closing Date: 01-04-2026

Why This Role MattersThe Clinical Research Coordinator (CRC) plays a crucial role in ensuring the smooth execution of clinical trials by bridging the gap between investigators, patients, and research teams. This position is essential for maintaining data integrity, patient safety, and regulatory compliance throughout the clinical study lifecycle. Working at a reputed institution like AIIMS Rishikesh offers valuable exposure to clinical research operations and contributes directly to advancements in healthcare and evidence-based medicine.Job DescriptionThe Clinical Research Coordinator will be responsible for supporting and managing clinical trial activities in accordance with study protocols, regulatory guidelines, and institutional policies. The role involves coordinating with investigators, managing study documentation, ensuring accurate data collection, and facilitating communication among stakeholders. The candidate will also play an important role in patient recruitment, informed consent processes, and maintaining compliance with Good Clinical Practice (GCP) standards.Key Features of the Role• Opportunity to work in a premier government medical institute• Direct involvement in clinical research and patient-centered studies• Exposure to regulatory compliance and ethical research practices• Hands-on experience with clinical trial documentation and coordination• Stable role with scope for learning and professional developmentResponsibilities• Coordinate and manage day-to-day clinical trial activities as per protocol• Assist investigators in patient recruitment, screening, and enrollment• Ensure proper informed consent is obtained and documented• Maintain accurate and up-to-date study records and case report forms (CRFs)• Monitor patient visits, follow-ups, and study timelines• Ensure compliance with GCP, ICH guidelines, and institutional policies• Handle regulatory documentation and assist during audits or inspections• Communicate effectively with sponsors, CROs, and internal teams• Maintain confidentiality and ensure data integrity throughout the study• Support reporting and documentation of adverse events and study outcomesRequired Qualifications• Any Degree, M.Pharm, or M.Sc Nursing from a recognized institution• Basic understanding of clinical research processes and regulations• Knowledge of GCP guidelines and ethical practices is preferredEducational Requirements• Bachelor’s Degree in Life Sciences / Pharmacy / Nursing or related field• Postgraduate qualification (M.Pharm / M.Sc Nursing) preferredExperience and Skills• Freshers or candidates with relevant clinical research exposure can apply• Strong organizational and documentation skills• Good communication and interpersonal abilities• Ability to coordinate with cross-functional teams• Attention to detail and ability to manage multiple tasks• Basic computer knowledge for documentation and reportingAge Eligibility• Minimum Age: 21 Years• Maximum Age: 45 Years• Age relaxation applicable as per government normsSalary Insights• Basic Pay: ₹27,000 per month• Opportunity to gain experience in a reputed government healthcare institution• Valuable exposure to clinical trials and research methodologiesCompany OverviewAIIMS Rishikesh is one of India’s leading medical institutions, known for excellence in healthcare, medical education, and research. The institute plays a significant role in advancing clinical research and providing high-quality patient care. Working here offers a structured environment with strong academic and clinical exposure.FAQs• Who can apply for this role?Candidates with a degree in Life Sciences, Pharmacy, or Nursing can apply.• Is prior experience mandatory?No, freshers with relevant knowledge or interest in clinical research can apply.• What is the key responsibility in this role?Managing and coordinating clinical trial activities while ensuring compliance.• What is the salary offered?The position offers a salary of ₹27,000 per month.• Is this a permanent role?This depends on the project or contractual terms defined by the institute.Application Tips• Highlight any clinical research, internship, or hospital experience• Mention knowledge of GCP, ICH guidelines, or clinical trials• Keep your resume focused on coordination, documentation, and patient handling skills• Ensure all academic and certification documents are updated• Apply before the deadline (25 March 2026) to avoid missing the opportunityApplication Deadline: 25-03-2026Official Notification Click Here

Why This Role MattersThe Young Professional role offers an excellent opportunity for early-career candidates to contribute to cutting-edge research, technical projects, and innovation-driven initiatives. This position is ideal for individuals looking to build a strong foundation in engineering, pharmaceutical sciences, or technology-driven domains while working in a structured and research-oriented environment. It plays a key role in supporting project execution, innovation, and scientific advancement within the organization.Job DescriptionThe Young Professional will be responsible for assisting in technical, research, and project-based activities across relevant departments. The role involves contributing to ongoing projects, supporting data analysis, preparing reports, and ensuring that all assigned tasks are executed efficiently within defined timelines. Candidates will work closely with cross-functional teams and gain exposure to real-world applications in engineering, pharmaceutical, or research domains.Key Features of the Role:• Opportunity to work in a research-driven and innovation-focused environment• Exposure to interdisciplinary projects in engineering and pharmaceutical sciences• Hands-on experience in technical execution and project support• Learning and development opportunities through real-time project involvement• Collaborative work culture with cross-functional team engagementResponsibilities• Assist in execution of technical and research projects as per organizational requirements• Support data collection, analysis, and interpretation for ongoing studies or projects• Prepare technical reports, presentations, and documentation• Coordinate with internal teams to ensure smooth project workflow• Maintain compliance with organizational standards and project guidelines• Contribute to innovation, problem-solving, and process improvement initiatives• Ensure timely completion of assigned tasks and deliverablesRequired Qualifications• Basic understanding of engineering principles, pharmaceutical sciences, or related technical fields• Ability to analyze data and interpret results effectively• Strong organizational and problem-solving skills• Good communication and teamwork abilities• Willingness to learn and adapt in a dynamic work environmentEducational Requirements:• B.E./B.Tech, M.E./M.Tech or B.Pharm from a recognized institutionExperience and Skills:• Freshers or candidates with limited experience can apply• Strong analytical and technical aptitude• Good knowledge of project execution and documentation practices• Proficiency in basic computer applications (MS Office, reporting tools, etc.)• Ability to work independently as well as in a teamAge Eligibility:• Minimum Age: 21 years• Maximum Age: 45 years• Age relaxation applicable as per organizational normsSalary Insights• Salary will be as per organizational standards and experience level• Additional benefits may include learning opportunities, project exposure, and professional development supportCompany OverviewThe hiring organization is a reputed research and development institute committed to scientific innovation and technological advancement. It provides a platform for young professionals to contribute to impactful projects while building strong technical expertise in their respective domains.FAQs• Who can apply for this role?Candidates with B.E./B.Tech, M.E./M.Tech or B.Pharm qualifications are eligible.• Is prior experience required?Freshers and candidates with minimal experience can apply.• Is there any application fee?• General/OBC: ₹200• SC/ST: No fee• What is the application timeline?• Start Date: 20 March 2026• Last Date: 09 April 2026• What kind of work will I be doing?You will support research, technical execution, documentation, and project coordination activities.Application Tips• Highlight your academic projects and technical skills clearly in your resume• Focus on analytical abilities and problem-solving experience• Keep all educational and identity documents ready before applying• Apply well before the deadline to avoid last-minute issues• Prepare for basic technical and aptitude-based interview questionsImportant Dates:Starting date: 20-03-2026Closing date: 09-04-2026Official Notification and Application Form Click Here

Why This Role MattersThe Assistant Sub Inspector (ASI) position under the SSB Notification 2026 is a critical role that supports operational efficiency, healthcare services, and administrative coordination within the organization. This role ensures smooth execution of duties across healthcare and support functions, contributing to both workforce well-being and institutional effectiveness. It offers a stable government career with structured growth, making it an attractive opportunity for candidates from healthcare and allied backgrounds.Job DescriptionThe Assistant Sub Inspector will be responsible for supporting healthcare services, administrative duties, and operational coordination as per departmental requirements. Depending on the assigned role, candidates may be involved in clinical assistance, pharmacy-related tasks, or general support functions within the organization. The position requires discipline, adaptability, and the ability to work in a structured environment aligned with government protocols.Key Features of the Role:• Government job with structured pay scale and long-term stability• Opportunities for candidates from healthcare and allied backgrounds• Multi-functional role involving healthcare, administrative, and support duties• Exposure to organized systems, compliance standards, and operational workflows• Career progression as per government norms and internal promotionsResponsibilities• Assist in healthcare or support services based on assigned department• Perform pharmacy-related, dental assistance, or basic clinical tasks where applicable• Maintain accurate records, documentation, and reports• Ensure compliance with organizational policies and operational guidelines• Support senior officers in administrative and operational duties• Coordinate with internal teams for smooth workflow and task execution• Maintain discipline, efficiency, and professionalism in all assigned activitiesRequired Qualifications• Candidates must possess one of the following qualifications:• Bachelor of Dental Surgery (BDS)• Diploma in relevant field• Diploma in Pharmacy (D. Pharm)• 12th Pass (for specific support roles)Educational Requirements:• Recognized qualification from a valid board or university• Relevant technical or healthcare background preferred for specialized rolesExperience and Skills:• Basic understanding of healthcare, pharmacy, or administrative functions• Good communication and interpersonal skills• Ability to work in a disciplined and structured environment• Strong organizational and record-keeping skills• Adaptability and willingness to handle multiple responsibilities• Teamwork and coordination abilitiesAge Eligibility:• Minimum Age: 18 Years• Maximum Age: 45 Years• Age relaxation applicable as per government normsSalary Insights• Pay Scale: ₹29,200 – ₹92,300 per month• Additional government allowances and benefits as applicable• Long-term financial stability with structured incrementsCompany OverviewThe Sashastra Seema Bal (SSB) is a government organization responsible for maintaining border security and supporting internal operations. Known for its disciplined structure and commitment to national service, SSB provides excellent career opportunities with stability, growth, and benefits aligned with government standards. Working with SSB offers individuals a chance to contribute to national service while building a secure professional future.FAQsQ1. Who can apply for the ASI role?Candidates with BDS, Diploma, D. Pharm, or 12th qualification (as per role requirement) can apply.Q2. What is the application fee?• General/OBC: ₹100• SC/ST/Female: No feeQ3. What is the salary range?The salary ranges from ₹29,200 to ₹92,300 per month.Q4. What is the age limit?Candidates must be between 18 to 45 years, with relaxation as per norms.Q5. Is this a permanent government job?Yes, it offers a stable government career with benefits and growth opportunities.Application Tips• Ensure eligibility criteria are met before applying• Keep all educational and identity documents ready• Fill out the application form accurately without errors• Apply before the deadline to avoid last-minute issues• Prepare for selection stages as per official guidelinesImportant Dates• Application Start Date: 21-03-2026• Application Closing Date: 20-04-2026Official Notification Click Here

Why This Role MattersThis role is essential in delivering safe and effective pharmaceutical care to ex-servicemen and their families under the ECHS healthcare system. As a Pharmacist, you will ensure proper medication dispensing, patient counseling, and adherence to treatment protocols, directly contributing to improved patient outcomes and healthcare quality.Job DescriptionEx-Servicemen Contributory Health Scheme (ECHS) is inviting applications for the position of Pharmacist in Mumbai. This role offers an opportunity to work in a structured government healthcare setup focused on delivering quality medical services to veterans and their dependents.Key Features of the Role:• Government healthcare job with stable work environment• Direct involvement in patient care and medication management• Opportunity to serve ex-servicemen and their families• Fixed salary structure with defined responsibilities• Professional exposure to clinical and retail pharmacy practicesResponsibilities• Dispense medications accurately as per prescriptions• Ensure proper labeling, storage, and handling of medicines• Provide patient counseling on dosage, usage, and side effects• Maintain inventory and ensure availability of essential medicines• Follow standard pharmacy practices and regulatory guidelines• Maintain records of dispensed medications and stock levels• Coordinate with doctors and healthcare staff for patient care• Ensure compliance with safety and hygiene standardsRequired Qualifications• Knowledge of pharmaceutical drugs and dispensing practices• Understanding of basic clinical pharmacy and patient counseling• Familiarity with inventory and stock management• Attention to detail and accuracy in dispensingEducational Requirements:• Diploma in Pharmacy (D. Pharm)Experience and Skills:• Freshers or candidates with relevant pharmacy experience can apply• Good communication and interpersonal skills• Ability to work in a healthcare team environment• Basic knowledge of pharmacy regulations and practices• Responsible and patient-focused approachAge Eligibility:• Minimum Age: 18 years• Maximum Age: 45 yearsSalary Insights• Monthly Salary: ₹36,500 (Fixed)Company OverviewEx-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative under the Ministry of Defence, designed to provide comprehensive healthcare services to ex-servicemen and their dependents through a network of polyclinics, empanelled hospitals, and medical facilities across the country.FAQs• What is the last date to apply?10 April 2026• What qualification is required?Diploma in Pharmacy (D. Pharm)• Is experience mandatory?Not strictly required; freshers may apply• What is the salary offered?₹36,500 per month (fixed)• What type of job is this?Government healthcare pharmacist roleApplication Tips• Ensure your D. Pharm certificate and registration are valid• Prepare documents including resume, ID proof, and certificates• Revise basics of drug dispensing and patient counseling• Highlight any prior pharmacy or hospital experience• Apply before the deadline to avoid last-minute issuesApplication Deadline: 10-04-2026Official Notification Click Here

Why This Role MattersThis opportunity plays a vital role in advancing biologics and plasma-derived therapies, which are essential for treating complex and life-threatening conditions. By working in production, quality, and microbiology functions, you contribute directly to ensuring the safety, efficacy, and quality of critical biopharmaceutical products.Job DescriptionICHOR Biologics Pvt. Ltd. is conducting a mega walk-in drive to hire professionals across multiple departments at its Genome Valley facility in Hyderabad. This role offers hands-on exposure to biologics manufacturing, quality control, formulation, and microbiology within a GMP-regulated environment.Key Features of the Role:• Opportunity to work in the fast-growing biologics and plasma-derived therapies sector• Exposure to advanced plasma fractionation and biopharma manufacturing technologies• Multiple openings across Production, QC, Formulation, and Microbiology• Strong career growth in high-demand biopharmaceutical roles• Collaborative and innovation-driven work environmentResponsibilities• Perform production activities in biologics manufacturing processes• Conduct quality control testing and maintain accurate documentation• Support formulation development and process optimization activities• Carry out microbiological analysis and ensure sterile environment compliance• Ensure adherence to GMP and regulatory guidelines across all operations• Maintain batch records, reports, and technical documentation• Coordinate with cross-functional teams for smooth workflow execution• Support IT systems and data handling activities where applicableRequired Qualifications• Basic understanding of biologics manufacturing or pharmaceutical processes• Knowledge of GMP and regulatory compliance standards• Familiarity with laboratory practices, documentation, and quality systemsEducational Requirements:• B.Sc / M.Sc• B.Pharm / M.Pharm• DiplomaExperience and Skills:• 1 to 8 years of experience in pharma or biologics industry• Freshers with relevant qualifications may be considered for junior roles• Strong analytical and problem-solving skills• Good communication and teamwork abilities• Ability to work in a regulated manufacturing or laboratory environment• Attention to detail and documentation accuracySalary Insights• Estimated salary range: ₹2.5 LPA – ₹6.5 LPA (based on role and experience)Company OverviewICHOR Biologics Pvt. Ltd. is a rapidly growing player in the plasma-derived biopharmaceutical segment. The company focuses on developing life-saving therapies through an integrated platform that includes plasma collection, fractionation, and product development aligned with global standards.FAQs• What departments are hiring?Production, Quality Control (Biologics), Formulation, and Microbiology.• Who can apply for this role?Candidates with, B.Pharm, M B.Sc, M.Sc, .Pharm or Diploma qualifications.• Is prior biologics experience required?Preferred, but candidates with relevant pharma experience may also apply.• What is the hiring mode?Direct walk-in interview process.• What is the career growth path?Operator/Executive → Senior Executive → Team Lead → Manager in Biopharma OperationsApplication Tips• Carry updated resume, educational certificates, and ID proof for the walk-in• Highlight any experience in biologics, QC, microbiology, or production• Revise GMP guidelines, aseptic practices, and basic biopharma concepts• Be prepared to discuss your role in previous manufacturing or lab work• Reach early to avoid long queues during the walk-in drive

Why This Role MattersThis role is critical in ensuring timely regulatory approvals for pharmaceutical products across international markets. By managing submissions, lifecycle activities, and compliance requirements, you directly contribute to product availability, regulatory success, and global expansion of medicines.Job DescriptionSun Pharma is hiring an Executive – Regulatory Affairs for its R&D1 Regulatory Affairs division in Baroda. This role focuses on handling regulatory submissions, dossier preparation, lifecycle management, and compliance for MENA markets, ensuring smooth approvals and adherence to global regulatory standards.Key Features of the Role:• Exposure to international regulatory markets (MENA, South Africa)• Hands-on experience in CMC dossier preparation and submissions• Involvement in lifecycle management and regulatory strategy• Cross-functional collaboration with R&D, QA, and manufacturing teams• Strong foundation for global regulatory affairs careerResponsibilities• Prepare and review CMC (Chemistry, Manufacturing and Controls) dossiers for new submissions and renewals• Review development reports, scale-up reports, specifications, stability protocols, and artworks before exhibit batch initiation• Draft and submit responses to regulatory deficiencies and queries for timely product approvals• Manage lifecycle activities including variations for API changes, manufacturing site changes, and product harmonization• Ensure compliance with country-specific regulatory requirements for MENA and South Africa markets• Prepare and circulate approval packages along with product history sheets to stakeholders• Maintain accurate regulatory documentation in centralized repositories• Assess regulatory impact of change controls, variations, and updatesRequired Qualifications• Strong understanding of regulatory submission processes and lifecycle management• Knowledge of CMC documentation and global regulatory guidelines• Familiarity with dossier preparation and compliance requirementsEducational Requirements:• M.Sc or M.PharmExperience and Skills:• 1 to 4 years of experience in Regulatory Affairs• Experience in handling submissions for international markets preferred• Good understanding of pharmaceutical development documentation• Strong attention to detail and documentation skills• Effective communication and stakeholder coordination abilities• Ability to manage multiple regulatory projects and timelinesSalary Insights• Estimated salary range: ₹4 LPA – ₹8 LPA (based on experience and skills)Company OverviewSun Pharma is one of the largest pharmaceutical companies in India and a global leader in specialty generics. The company operates across multiple international markets, delivering high-quality, affordable medicines while maintaining strong regulatory and compliance standards.FAQs• What markets will I work on?Primarily MENA regions and South Africa regulatory markets.• What type of regulatory work is involved?CMC dossier preparation, submissions, query responses, and lifecycle management.• Is prior international regulatory experience required?Preferred but not mandatory for candidates with strong regulatory fundamentals.• What is the career path?Executive RA → Senior Executive → Assistant Manager → Regulatory Affairs ManagerApplication Tips• Highlight your experience in CMC dossier preparation and submissions• Mention any exposure to international markets (MENA, US, EU, etc.)• Showcase your role in handling regulatory queries and lifecycle management• Emphasize documentation accuracy and compliance knowledge• Include examples of cross-functional collaboration with R&D or QA teams

Why This Role MattersThis role plays a vital part in ensuring smooth execution of clinical trials by managing legally compliant agreements between sponsors, CROs, and research sites. By handling global clinical contracts and regulatory documentation, you contribute directly to accelerating clinical research timelines and ensuring compliance with international standards.Job DescriptionClario is hiring a Contract Specialist for its Bangalore or remote setup. This role focuses on managing end-to-end clinical and commercial contracting processes, supporting global clinical trial operations, and ensuring compliance with regulatory and legal frameworks.Key Features of the Role:• Exposure to global clinical trial agreements and legal frameworks• Opportunity to work in a remote or hybrid environment• Involvement in high-impact clinical research projects• Strong cross-functional collaboration with legal, clinical, and operations teams• Career growth in clinical legal and contract management domainResponsibilities• Draft, review, and negotiate contracts including CDAs, Work Orders (WOs), Start-Up Agreements (SUAs), and Letters of Intent (LOIs)• Support negotiation of Master Service Agreements (MSAs), Stand-Alone Agreements (SAAs), Data Privacy Agreements (DPAs), and Quality Agreements• Conduct legal review of Change Orders (COs) and ensure compliance with contractual terms• Manage end-to-end contract lifecycle using Salesforce or contract management systems• Track escalations for non-standard contract clauses and coordinate with subject matter experts (SMEs)• Maintain accurate, compliant, and audit-ready documentation• Handle electronic signatures and contract execution workflows• Support audits, regulatory inspections, and SOP compliance processes• Collaborate with cross-functional teams including legal, clinical operations, and project managementRequired Qualifications• Strong understanding of contract lifecycle management• Knowledge of clinical trial agreements and regulatory frameworks• Familiarity with global compliance and documentation standardsEducational Requirements:• Bachelor’s degree (Law, Life Sciences, Pharmacy, or related field preferred)Experience and Skills:• Minimum 3+ years of experience in commercial or clinical contracting• Experience in Pharma, CRO, or Clinical Research industry• Hands-on experience with agreements such as MSA, CDA, and DPA• Proficiency in Microsoft Word (advanced drafting) and Excel (tracking/reporting)• Experience with Salesforce or contract lifecycle management systems• Strong attention to detail and ability to manage deadlines• Excellent communication and stakeholder management skillsSalary Insights• Estimated salary range: ₹8 LPA – ₹14 LPA (based on experience and expertise)Company OverviewClario is a global leader in clinical trial technology and evidence generation. The company supports pharmaceutical and biotech organizations by providing data-driven solutions that enhance clinical development and accelerate the delivery of life-saving therapies worldwide.FAQs• What types of contracts will I handle?You will manage clinical agreements such as CDAs, MSAs, DPAs, and study-related contracts.• Is prior CRO experience required?Preferred but not mandatory if you have strong contracting experience in pharma or related domains.• What tools are commonly used in this role?Salesforce and other contract lifecycle management systems are widely used.• What is the career growth path?Contract Specialist → Senior Contract Specialist → Contract Manager → Legal/Clinical Operations LeadApplication Tips• Highlight your experience with clinical contracts (CDA, MSA, DPA)• Showcase your role in contract negotiation and lifecycle management• Mention tools like Salesforce or any contract management software• Emphasize compliance knowledge and audit readiness experience• Provide examples of working with cross-functional or global teams

Why This Role MattersThis role is critical in ensuring that pharmaceutical products meet stringent regulatory requirements for the US market. By managing ANDA submissions, post-approval changes, and compliance activities, you directly support timely product approvals, lifecycle management, and patient access to safe and effective medicines.Job DescriptionLupin is hiring an Executive – Regulatory Affairs (US ANDA) for its Airoli (Mumbai) location. This role focuses on handling regulatory submissions for Oral Solid Dosage (OSD) products in the US market, ensuring compliance with USFDA requirements, and supporting lifecycle management activities.Key Features of the Role:• Exposure to US regulatory framework (USFDA)• Hands-on experience with ANDA submissions and lifecycle management• Involvement in labeling updates and regulatory strategy• Opportunity to work on global pharmaceutical products• Cross-functional collaboration with R&D, manufacturing, and QA teamsResponsibilities• Lead regulatory submissions for Oral Solid Dosage (OSD) products for the US market• Prepare and submit ANDA dossiers in compliance with regulatory guidelines• Respond to product deficiencies and queries raised by USFDA• Manage post-approval submissions and annual reports for approved products• Drive labeling updates in alignment with Reference Listed Drug (RLD) changes• Provide regulatory support for PADER (Periodic Adverse Drug Experience Reports)• Review documentation across product development, scale-up, and commercialization stages• Ensure regulatory compliance for externally manufactured products• Collaborate with cross-functional teams for submission readiness and complianceRequired Qualifications• Strong understanding of US regulatory requirements (ANDA, USFDA guidelines)• Knowledge of lifecycle management and post-approval changes• Familiarity with labeling requirements and pharmacovigilance reportingEducational Requirements:• Bachelor’s Degree in Pharmacy (B.Pharm)Experience and Skills:• 2–3 years of experience in regulatory submissions for OSD (US market)• Hands-on experience in ANDA filing and deficiency response handling• Strong documentation and technical writing skills• Good understanding of pharmaceutical development lifecycle• Effective communication and stakeholder management skills• Ability to work in cross-functional teams• Problem-solving mindset with attention to detailSalary Insights• Estimated salary range: ₹4 LPA – ₹8 LPA (based on experience and company standards)Company OverviewLupin is one of India’s leading pharmaceutical companies with a strong global presence. Known for its expertise in generics and complex formulations, Lupin operates in multiple international markets including the US, offering employees exposure to global regulatory environments and advanced pharmaceutical development practices.FAQs• What is ANDA in this role?ANDA (Abbreviated New Drug Application) is required for approval of generic drugs in the US market.• Is USFDA experience mandatory?Yes, experience with US regulatory submissions (especially ANDA) is essential.• What is RLD?Reference Listed Drug (RLD) is the innovator drug used as a reference for generic drug approval.• What is the career growth path?Executive → Senior Executive → Assistant Manager → Manager (Regulatory Affairs)Application Tips• Highlight your experience with ANDA submissions and USFDA interactions• Mention specific involvement in deficiency responses or labeling updates• Showcase your understanding of OSD formulations and lifecycle management• Emphasize documentation and regulatory writing skills• Prepare examples of cross-functional collaboration and compliance handling

Why This Role MattersThis role plays a vital part in maintaining quality systems and regulatory compliance within pharmaceutical manufacturing. By managing LIMS and driving QC training initiatives, you ensure data integrity, audit readiness, and adherence to global standards like USFDA and GMP—directly contributing to product quality and patient safety.Job DescriptionOxalis Labs is hiring for the position of Quality Control Officer/Senior Officer in the Training/LIMS section. This role focuses on managing laboratory systems, conducting training programs, and ensuring compliance with global regulatory standards in a USFDA-approved manufacturing environment.Key Features of the Role:• Opportunity to work in a USFDA-approved pharmaceutical facility• Hands-on experience with LIMS (Laboratory Information Management System)• Involvement in QC training and capability development• Exposure to audits and global regulatory standards• Strong career growth in Quality Control and compliance functionsResponsibilities• Manage and maintain Laboratory Information Management System (LIMS)• Conduct training programs for QC team members and track training effectiveness• Ensure compliance with USFDA, GMP, and other regulatory guidelines• Handle documentation related to QC processes and training records• Support internal and external audits, including regulatory inspections• Maintain data integrity and accuracy within QC systems• Coordinate with cross-functional teams for continuous quality improvement• Monitor adherence to SOPs and quality standardsRequired Qualifications• Strong understanding of QC processes and regulatory compliance• Knowledge of LIMS and training systems preferred• Familiarity with GMP and data integrity principlesEducational Requirements:• B.Pharm• M.Pharm• M.Sc (relevant specialization)Experience and Skills:• 3–6 years of experience in Quality Control• Hands-on experience in LIMS and/or QC training activities preferred• Strong documentation and audit handling skills• Good communication and training delivery capability• Attention to detail and problem-solving mindset• Ability to work in cross-functional teams• Understanding of regulatory inspections and compliance frameworksSalary Insights• Estimated salary range: ₹3.5 LPA – ₹6.5 LPA (based on experience)Company OverviewOxalis Labs is a USFDA-approved pharmaceutical manufacturing organization known for its adherence to global quality standards. The company offers a strong platform for professionals to gain exposure to regulatory environments, advanced quality systems, and continuous learning opportunities in the pharma industry.FAQs• Is LIMS experience mandatory?It is preferred, especially for candidates applying for senior roles.• What kind of audits will I be exposed to?You may work on USFDA audits and other regulatory inspections.• Is this a pure QC role?It is a specialized QC role focusing on LIMS management and training functions.• What is the career growth path?QC Officer → Senior Officer → QC Manager → Quality Systems/Compliance LeadApplication Tips• Highlight your experience with LIMS and QC documentation• Mention any involvement in audits or regulatory inspections• Showcase training or mentoring experience if applicable• Emphasize knowledge of GMP and data integrity• Prepare examples of process improvements or quality initiatives

Why This Role MattersThis walk-in opportunity is significant for candidates aiming to build a strong career in API (Active Pharmaceutical Ingredient) manufacturing. Roles in Production and Quality Control are essential to ensure drug quality, regulatory compliance, and efficient manufacturing—directly impacting patient safety and pharmaceutical excellence.Job DescriptionSekhmet Pharmaventures is conducting a walk-in drive for Production and Quality Control roles in API manufacturing. The hiring process is direct and fast-tracked, offering both freshers and experienced professionals a chance to join a GMP-regulated pharmaceutical environment.Key Features of the Role:• Direct walk-in opportunity with faster selection process• Openings for both freshers and experienced candidates• Exposure to API manufacturing and GMP practices• Opportunity to work in Production and Quality Control departments• Career growth in core pharmaceutical manufacturingResponsibilitiesProduction Department• Handle API manufacturing processes and batch operations• Monitor production equipment and ensure smooth functioning• Maintain batch records and production documentation• Ensure compliance with GMP and safety guidelines• Coordinate with QA/QC teams for quality assuranceQuality Control (QC)• Perform analytical testing of raw materials and finished products• Maintain laboratory instruments and documentation• Follow SOPs and regulatory guidelines• Support validation and quality-related activities• Ensure compliance with quality and regulatory standardsRequired Qualifications• Knowledge of GMP and pharmaceutical processes• Basic understanding of analytical testing (for QC roles)• Ability to work in a manufacturing environmentEducational Requirements:• M.Sc in Chemistry• B.PharmExperience and Skills:• Production: 4–5 years of experience in API manufacturing• Quality Control: Freshers eligible• Strong documentation and compliance understanding• Attention to detail and quality-focused mindset• Good communication and teamwork skills• Ability to follow SOPs and regulatory standardsSalary Insights• QC Freshers: ₹2.5 LPA – ₹3.5 LPA• Production (Experienced): ₹4 LPA – ₹6 LPACompany OverviewSekhmet Pharmaventures is an emerging pharmaceutical organization focused on API manufacturing and development. The company offers opportunities to work in GMP-compliant environments, providing hands-on exposure to core pharmaceutical production and quality processes.FAQs• Is this a walk-in interview?Yes, candidates can directly attend the interview without prior application.• Are freshers eligible?Yes, freshers can apply for Quality Control roles.• What documents should I carry?Updated resume, educational certificates, and valid ID proof.• Is prior API experience mandatory?Yes, for Production roles (4–5 years required), but not for QC roles.Application Tips• Carry multiple copies of your updated resume• Revise basic GMP, SOPs, and analytical concepts before attending• Be prepared to discuss your academic or work experience clearly• Dress professionally and arrive early to avoid delays• Highlight any hands-on lab or production exposureWalk-In Interview Details• Date: 23 March 2026• Time: 10:00 AM to 4:00 PM• Venue: Anjan Drug Private Limited, Plot No. 109, 110, 115 & 116, SIDCO Pharmaceutical Industrial Estate, OMR, Alathur – 603110Important Notes• Opportunity is open only for male candidates as per company requirement• Carry all required documents for verification• Early arrival is recommended for smooth interview process

Why This Role MattersThis role is critical in ensuring the smooth execution of clinical research by managing and qualifying GxP-compliant vendors. By supporting vendor selection, onboarding, and governance, you directly contribute to the quality, compliance, and efficiency of clinical trials—ultimately impacting the successful delivery of innovative therapies to patients worldwide.Job DescriptionThe Global Partnering Associate supports vendor management and partnering activities within clinical research programs. Working closely with the Global Partnering Manager and cross-functional teams, you will be responsible for vendor qualification, compliance tracking, and coordination across internal stakeholders and external partners during pre-award and post-award stages of clinical studies.Key Features of the Role:• Exposure to global clinical research and vendor management processes• Opportunity to work with international stakeholders and GxP vendors• Involvement in RFP processes and study start-up activities• Hands-on experience in compliance, audits, and risk management• Cross-functional collaboration across QA, Contracts, and Project Management teamsResponsibilities• Assist in identification, selection, qualification, and onboarding of GxP vendors• Maintain and update the approved vendor database and documentation• Coordinate with Contracts team for NDA execution with vendors• Collaborate with Quality Assurance (QA) to manage vendor audits and compliance status• Ensure vendor processes comply with global regulations (e.g., GDPR, UK Bribery Act)• Support RFP processes and vendor evaluation during study start-up phases• Coordinate with Project Managers for issue tracking and escalation management• Organize vendor governance calls, document meeting minutes, and track action items• Conduct internal surveys and gather feedback for continuous improvement• Participate in strategic initiatives within the Global Partnering functionRequired Qualifications• Strong understanding of vendor management and clinical research processes• Knowledge of GxP compliance and regulatory frameworks• Ability to manage multiple stakeholders and projects simultaneouslyEducational Requirements:• Bachelor’s degree in Science, Pharmacy, or related field• Master of Pharmacy (M.Pharm) or MBA preferred• PMP (Project Management Professional) certification is an added advantageExperience and Skills:• Minimum 4 years of experience in Vendor Management, Clinical Operations, or Project Management• Experience in Pharma, Biotech, or Clinical Research Organization (CRO) preferred• Strong analytical, organizational, and problem-solving skills• Excellent verbal and written communication skills• Proficiency in Microsoft Office tools (Word, Excel, PowerPoint, Teams)• Ability to work cross-functionally with global teams• Strong attention to detail and risk assessment capability• Passion for clinical research and continuous learningSalary Insights• Estimated salary range: ₹8 LPA – ₹14 LPA (depending on experience and organization)Company OverviewEmmes Group is a globally recognized clinical research organization with over four decades of experience in advancing medical research. The company specializes in areas such as cell and gene therapy, vaccines, infectious diseases, rare diseases, and neuroscience. With a strong focus on innovation and collaboration, Emmes partners with government bodies, biopharma companies, and research institutions to accelerate clinical development and improve patient outcomes worldwide.FAQs• Is this role technical or management-focused?It is a hybrid role combining operational, compliance, and project coordination responsibilities.• Do I need prior CRO experience?It is preferred but not mandatory if you have relevant vendor management or project experience.• What is GxP in this role?GxP refers to Good Practice guidelines (like GMP, GCP) ensuring quality and compliance in clinical research.• What career growth can I expect?Global Partnering Associate → Vendor Manager → Clinical Project Manager → Program ManagerApplication Tips• Highlight experience in vendor management, audits, or clinical operations• Showcase your knowledge of GxP and regulatory compliance• Emphasize stakeholder management and communication skills• Include examples of handling escalations or cross-functional coordination• Demonstrate familiarity with clinical trial processes and documentation

Why This Role MattersThis role is essential in safeguarding patient health by ensuring the continuous evaluation of drug safety throughout its lifecycle. As a Safety Physician, you play a vital role in pharmacovigilance, contributing to benefit-risk assessments, clinical development strategies, and regulatory compliance. Your expertise directly influences how safely medicines are developed, monitored, and used in real-world settings.Job DescriptionThe Safety Physician is responsible for overseeing pharmacovigilance activities, risk management planning, and clinical safety evaluations for assigned products. The role involves close collaboration with cross-functional teams to ensure accurate safety data interpretation, regulatory compliance, and implementation of risk minimization strategies.Key Features of the Role:• Involvement in global pharmacovigilance and risk management strategies• Exposure to clinical development and regulatory safety processes• Opportunity to contribute to benefit-risk assessments of drugs• Cross-functional collaboration with clinical, regulatory, and safety teams• Participation in high-impact safety decision-making processesResponsibilities• Conduct and support pharmacovigilance and risk management planning for assigned products• Contribute to benefit-risk assessments and preparation of Risk Management Plans (RMPs)• Provide clinical safety input into clinical development and study planning• Review and approve key clinical documents including protocols, investigator brochures, and informed consent forms• Participate in cross-functional teams addressing urgent safety concerns• Support establishment and functioning of Safety Review Teams• Analyze safety data and contribute to interpretation and risk evaluation• Ensure implementation of risk minimization strategies in study protocols and product labeling• Identify potential post-authorization safety studies (PASS) and notify leadership• Present safety findings in clinical and investigator meetings• Collaborate with product scientists and regulatory teams for safety decision-makingRequired Qualifications• Strong understanding of pharmacovigilance and clinical safety principles• Knowledge of regulatory requirements and drug development processes• Ability to analyze clinical and safety data effectively• Excellent communication and cross-functional collaboration skillsEducational Requirements:• MBBS / MD (Mandatory)Experience and Skills:• 1–2 years of experience in pharmacovigilance, clinical safety, or related domain• Understanding of benefit-risk assessment and risk management planning• Familiarity with clinical trial protocols and safety documentation• Strong analytical and medical review skills• Ability to work in cross-functional and global teams• Effective presentation and communication skills• Attention to detail and decision-making ability in safety-critical scenariosSalary Insights• Expected salary range: ₹10 LPA – ₹18 LPA (approx., depending on qualifications and experience)Company OverviewTata Consultancy Services (TCS) is a leading global IT services, consulting, and business solutions organization. Through its life sciences and healthcare division, TCS supports pharmacovigilance, clinical research, and regulatory services for global pharmaceutical companies, enabling safe and effective healthcare delivery.FAQs• Is clinical experience mandatory for this role?Clinical knowledge is essential, but prior pharmacovigilance experience is also valuable.• What is the difference between Safety Physician and Drug Safety Associate?A Safety Physician focuses on medical review and risk assessment, while associates handle case processing and data entry.• Does this role involve patient interaction?No, this is a non-clinical role focused on drug safety evaluation and regulatory activities.• What is the career progression?Safety Physician → Senior Safety Physician → Medical Safety Lead → Pharmacovigilance HeadApplication Tips• Highlight clinical knowledge and pharmacovigilance exposure in your CV• Emphasize experience with clinical protocols and safety data review• Showcase analytical thinking and decision-making skills• Mention any involvement in risk management or regulatory activities• Prepare for interviews on drug safety concepts and benefit-risk evaluation

Why This Role MattersThis role plays a critical part in ensuring patient safety by monitoring, evaluating, and reporting adverse drug reactions. As part of global pharmacovigilance operations, you contribute to maintaining the safe use of medicines and compliance with international regulatory standards. Your work directly impacts healthcare decisions, risk management, and overall drug safety surveillance.Job DescriptionThe Associate Safety Data Management Specialist is responsible for handling Individual Case Safety Reports (ICSRs), evaluating adverse event data, and ensuring accurate documentation and regulatory compliance. The role involves working in a structured pharmacovigilance environment, collaborating with cross-functional teams, and supporting global safety and regulatory strategies.Key Features of the Role:• Exposure to global pharmacovigilance systems and regulatory frameworks• Hands-on experience with ICSR processing and safety databases like ARGUS• Opportunity to work on clinical trial and post-marketing safety data• Involvement in medical review, data analysis, and regulatory submissions• Collaborative work environment with medical, regulatory, and safety teamsResponsibilities• Monitor drug, biologics, and medical device safety surveillance programs• Intake, evaluate, and process adverse event reports from various sources• Perform ICSR case processing including data entry, coding, and validation• Assess case validity, seriousness, causality, and listedness• Conduct duplicate checks and ensure accurate case prioritization• Draft and review case narratives for regulatory submissions• Determine appropriate workflows for case handling and processing• Perform follow-ups for missing or additional safety information• Review processed cases to ensure accuracy, completeness, and compliance• Support regulatory submissions by ensuring adherence to global guidelines• Analyze post-marketing safety data and medical literature• Collaborate with internal teams for data reconciliation and reporting• Maintain compliance with company SOPs and global pharmacovigilance regulationsRequired Qualifications• Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm / Pharm.D)• Basic understanding of pharmacovigilance and drug safety processes• Knowledge of medical terminology and adverse event reporting• Familiarity with global safety regulations and compliance standardsEducational Requirements:• B.Pharm / M.Pharm / Pharm.D (Mandatory)Experience and Skills:• 0–2 years of experience in pharmacovigilance or drug safety• Knowledge of ICSR processing and case handling workflows• Familiarity with ARGUS safety database (preferred)• Understanding of XML formats (E2B R2/R3) is an added advantage• Strong attention to detail and data accuracy skills• Good communication and documentation abilities• Ability to work in a structured, process-driven environment• Team collaboration and problem-solving skillsSalary Insights• Expected salary range: ₹3 LPA – ₹6 LPA (approx., based on experience and company standards)Company OverviewPfizer is a leading global pharmaceutical organization focused on innovation, drug safety, and improving patient outcomes. With a strong presence in medical and safety operations, the company plays a key role in advancing healthcare through evidence-based medicine and regulatory excellence.FAQs• Is prior pharmacovigilance experience mandatory?No, freshers with relevant knowledge can apply, though experience is preferred.• What tools are commonly used in this role?ARGUS safety database, XML-based reporting systems, and medical literature databases.• Is this a clinical or non-clinical role?This is a non-clinical role focused on drug safety and regulatory processes.• What is the career growth path?Drug Safety Associate → Senior PV Associate → Drug Safety Scientist → PV ManagerApplication Tips• Highlight knowledge of pharmacovigilance and ICSR processing in your CV• Mention any experience with ARGUS or safety databases• Emphasize attention to detail and documentation skills• Include certifications or training in drug safety (if any)• Prepare for interview questions on adverse event reporting and case processing

Why This Role MattersThe role of Associate Safety Data Management Specialist at Pfizer plays a critical part in ensuring patient safety and regulatory compliance across global pharmacovigilance systems. By processing and evaluating safety data, this position directly contributes to the safe and effective use of medicines worldwide. It supports evidence-based medical decisions and helps identify potential risks, ultimately protecting patient health and improving therapeutic outcomes.Job DescriptionThis position focuses on pharmacovigilance and drug safety operations, particularly Individual Case Safety Report (ICSR) processing. The candidate will be responsible for reviewing, validating, documenting, and managing safety data in compliance with global regulatory standards. The role also involves working with internal stakeholders and global teams to ensure high-quality data handling and timely reporting of safety information.Key Features of the Role:• Global exposure to pharmacovigilance and drug safety operations• Hands-on experience with ICSR case processing and safety databases• Opportunity to work in a hybrid work environment• Strong focus on regulatory compliance and data accuracy• Collaborative role involving cross-functional teamsResponsibilities• Review, assess, and process Individual Case Safety Reports (ICSRs) for accuracy and completeness• Evaluate case details including seriousness, validity, and special scenarios• Perform case triaging and determine appropriate workflows• Write and edit detailed case narratives• Conduct follow-ups for missing or incomplete safety information• Ensure compliance with global regulatory timelines and reporting standards• Review processed cases to verify consistency and accuracy• Identify complex cases and escalate as required• Collaborate with internal teams and stakeholders for safety data reconciliation• Maintain updated knowledge of pharmacovigilance regulations, SOPs, and safety databases• Ensure proper documentation and adherence to Pfizer policiesRequired Qualifications• Bachelor’s or Master’s degree in Pharmacy (B.Pharm, M.Pharm) or Pharm.D• Basic understanding of pharmacovigilance and drug safety processes• Knowledge of medical terminology and clinical conceptsEducational Requirements:• B.Pharm / M.Pharm / Pharm.D (Mandatory)Experience and Skills:• 1–2 years of experience in pharmacovigilance or ICSR processing• Knowledge of global drug safety regulations and reporting requirements• Familiarity with safety databases such as Argus (preferred)• Understanding of E2B formats (R2/R3) and XML-based safety data• Strong attention to detail and analytical thinking• Good written and verbal communication skills• Ability to work in a team-oriented and deadline-driven environment• Problem-solving skills with ability to handle complex safety casesSalary Insights• Competitive industry-standard salary (typically ₹3–6 LPA for this experience range in India)• Additional benefits may include performance bonuses, health insurance, and hybrid work flexibilityCompany OverviewPfizer is a globally recognized biopharmaceutical leader focused on discovering, developing, and delivering innovative medicines and vaccines. With a strong emphasis on patient safety, research excellence, and regulatory compliance, Pfizer continues to play a vital role in advancing healthcare outcomes worldwide. The company’s Worldwide Medical and Safety division is central to ensuring that all products meet the highest standards of safety and efficacy.FAQs• Is prior pharmacovigilance experience mandatory?Yes, 1–2 years of experience in ICSR processing or drug safety is required.• What tools are commonly used in this role?Safety databases like Argus and XML-based reporting systems (E2B formats).• Is this a remote role?This is a hybrid role, requiring a mix of remote and office-based work.• What is the career growth path?Roles such as Drug Safety Associate, Senior PV Specialist, and Medical Reviewer.• Is knowledge of regulations important?Yes, strong understanding of global pharmacovigilance regulations is essential.Application Tips• Highlight your experience in ICSR processing and safety databases• Mention knowledge of Argus, E2B formats, and pharmacovigilance workflows• Showcase attention to detail and compliance understanding• Include any certifications or training in drug safety or PV• Emphasize communication skills and ability to work in cross-functional teams

Why This Role MattersThis walk-in opportunity at Unichem Laboratories Ltd. offers candidates a strong entry and growth pathway in the pharmaceutical manufacturing sector, particularly in Oral Solid Dosage (OSD). With multiple openings across Production, Quality Control (QC), Quality Assurance (QA), and Engineering, this drive is ideal for professionals aiming to build expertise in regulated environments. Working in such roles ensures direct contribution to medicine quality, compliance, and patient safety, while also enhancing technical and operational skills aligned with industry standards like GMP.Job DescriptionUnichem Laboratories is conducting a walk-in interview to hire skilled professionals for various departments at its Baddi facility. Candidates will be responsible for executing department-specific operations such as manufacturing, analytical testing, quality compliance, and engineering maintenance. The roles require hands-on involvement in OSD processes, documentation, and adherence to regulatory requirements, ensuring smooth and compliant plant operations.Key Features of the Role:• Walk-in interview scheduled on 2nd April 2026 (Thursday)• Multiple openings across Production, QC, QA, and Engineering• Location: Baddi, Himachal Pradesh• Exposure to regulated pharmaceutical manufacturing environment• Opportunity to work with industry-standard equipment and processes• Roles suitable for ITI, Diploma, B.Sc, B.Pharm, and Engineering graduatesResponsibilities• Production: Operate compression and granulation machines, execute batch manufacturing, and maintain production records as per SOPs• Quality Control: Perform analysis of raw materials and finished products, ensure proper documentation, and calibrate lab instruments• Engineering: Manage HVAC systems, water systems, and utilities, and perform preventive and breakdown maintenance• Quality Assurance: Conduct IPQA activities, handle documentation and validation processes, and ensure regulatory compliance• Ensure adherence to GMP guidelines and maintain audit readiness• Support cross-functional coordination for smooth manufacturing and quality operationsRequired Qualifications• ITI / Diploma / B.Sc / B.Pharm / BE• Relevant experience in OSD (Oral Solid Dosage) manufacturingEducational Requirements:• Technical qualifications (ITI/Diploma) for technician and engineering roles• Science or pharmacy background (B.Sc/B.Pharm) for QC and QA roles• Engineering degree/diploma for utility and maintenance functionsExperience and Skills:• 2–5 years of experience depending on the role• Hands-on experience in OSD manufacturing is essential• Strong knowledge of GMP and pharmaceutical processes• Good documentation and reporting skills• Familiarity with equipment handling and troubleshooting• Ability to work in a regulated and compliance-driven environmentSalary Insights• Estimated salary range: ₹2.5 LPA – ₹5.5 LPA• Salary depends on role, qualification, and experience• Additional benefits include career growth, regulated exposure, and competitive compensationCompany OverviewUnichem Laboratories Ltd. is a well-established pharmaceutical organization known for its strong presence in formulation development and manufacturing. The company focuses on quality-driven production and compliance with global regulatory standards. With manufacturing facilities catering to both domestic and international markets, Unichem provides a robust platform for professionals to gain industry-relevant experience and long-term career growth.FAQs• Who can attend the walk-in interview?Candidates with relevant qualifications (ITI/Diploma/B.Sc/B.Pharm/Engineering) and OSD experience can attend• Is prior pharma experience mandatory?Yes, relevant OSD experience is required for most roles• What documents should I carry?Updated resume, educational certificates, experience letters, and ID proof• Is this a permanent role?Yes, these are full-time roles based on department requirements• What is the work location?Baddi, Himachal PradeshApplication Tips• Reach the venue early between 09:00 AM – 05:30 PM to avoid last-minute rush• Carry multiple copies of your resume and all supporting documents• Revise key concepts of GMP, OSD processes, and your domain expertise• Be prepared to discuss hands-on experience with equipment and procedures• Dress professionally and be ready for on-the-spot interviewsWalk-In Interview DetailsDate: 2nd April 2026 (Thursday)Time: 09:00 AM to 05:30 PMVenue: VPO Batholi Kalan, Baddi – 173205, Himachal Pradesh

Why This Role MattersThe Analyst Clinical Label Management role at Novartis is essential for ensuring accuracy, compliance, and traceability in clinical trial labeling processes. Proper labeling of Investigational Medicinal Products (IMP) is critical for patient safety, regulatory compliance, and trial integrity. This role supports global clinical operations by ensuring that labeling activities are executed with precision and aligned with regulatory and study-specific requirements.Job DescriptionThe Analyst Clinical Label Management is responsible for executing labeling activities for clinical trials, including label design, documentation, and compliance monitoring. This role involves close collaboration with internal teams and external stakeholders to ensure that all labeling processes are completed accurately, on time, and in line with global regulatory standards and study protocols.Key Features of the Role:• Role based in India with involvement in global clinical trials• Focus on clinical trial labeling and IMP management• Strong alignment with regulatory compliance and GMP standards• Interaction with supply chain, clinical, and external vendors• Opportunity to work on global labeling strategies and processes• Exposure to documentation systems and compliance audits• Structured and process-driven work environmentResponsibilities• Generate and design labels for Investigational Medicinal Products (IMP)• Prepare randomization lists and schedules as per study requirements• Ensure labeling aligns with study design, pack design, and regulatory standards• Manage and track assigned tasks and tickets for workflow continuity• Upload and maintain study-related documents and templates in systems• Provide regular updates and status reports to the Label Lead• Maintain and update Phrase Library for country-specific requirements• Ensure compliance with Health Authority (HA) regulations and company standards• Perform GMP line unit checks (if certified) and document results• Identify and report deviations or quality issues• Collaborate with internal teams (clinical supply, supply chain) and external vendors• Support audit and inspection readiness• Participate in projects, networks, and continuous improvement initiativesRequired Qualifications• Strong understanding of clinical trial processes and labeling requirements• Knowledge of GMP, HSE, and regulatory compliance standards• Good project management and organizational skills• Strong communication and stakeholder management abilities• Ability to work in cross-functional and interdisciplinary teamsEducational Requirements:• Degree in Science, Engineering, or equivalent fieldExperience and Skills:• Minimum 2+ years of experience in pharmaceutical or chemical industry• OR 3+ years of relevant experience in labeling or related field• Experience in clinical trial supply or labeling processes preferred• Basic project management and planning skills• Strong problem-solving and analytical abilities• Good documentation and reporting skills• Familiarity with regulatory and compliance requirements• Strong interpersonal and communication skillsSalary Insights• Competitive salary based on experience and industry standards• Additional benefits including performance incentives and career development opportunitiesCompany OverviewNovartis is a leading global healthcare company focused on reimagining medicine to improve and extend people’s lives. With a strong presence in clinical research, innovation, and regulatory excellence, Novartis continues to deliver high-quality healthcare solutions across the world.FAQs• What is the main focus of this role?Clinical trial labeling and compliance for investigational products.• Is prior labeling experience required?Preferred, but relevant pharma or clinical experience is acceptable.• Does the role involve regulatory compliance?Yes, it involves adherence to GMP and Health Authority requirements.• Will I work with global teams?Yes, the role involves collaboration with global stakeholders.• What qualifications are required?A degree in science, engineering, or related field.Application Tips• Highlight experience in clinical trials, labeling, or supply chain• Showcase knowledge of GMP, HSE, and regulatory standards• Emphasize attention to detail and documentation skills• Include examples of cross-functional collaboration• Demonstrate project management and organizational abilities• Tailor your CV to reflect compliance and quality-focused experience