Pharmacy Jobs

Roles & Responsibilities: • Operate advanced analytical instruments such as HPLC, GC, ICP-MS for testing raw materials, finished products, and dosage forms. • Perform method development, validation, and transfer for assays, related compounds, dissolution, and residual solvents. • Prepare method development reports, study protocols, TT reports, and COA for development samples. • Conduct stability analysis as per protocols and maintain accurate documentation in compliance with GLP and GDP. • Participate in investigations, support continuous lab development through training, and adhere to SOPs. • Manage laboratory inventory, raise procurement requests, and attend technical workshops to explore new techniques. Qualification: • Master’s degree in Science (MS/M.Sc) or M. Pharma preferred. Experience: • 5–7 years of experience in analytical method development, validation, and laboratory operations. Skills: • Good Laboratory Practices (GLP), Data Integrity, and Compliance – Advanced. • Analytical Method Development & Validation – Intermediate. • Documentation & Data Review, Interpretation, and Statistical Analysis – Intermediate. • Stability Study Management – Advanced. • Electronic Lab Notebook (ELN)/LIMS Management – Advanced. • Adapts to organizational growth – Intermediate. About the Organisation: Amneal Pharmaceuticals is a global pharmaceutical company committed to innovation, quality, and compliance, delivering high-quality medicines while fostering a diverse and inclusive workplace.

Roles & Responsibilities: • Develop and implement regulatory strategies for new and existing products, including NDA/sNDA filings and product lifecycle maintenance. • Manage ongoing renewals, variations, labeling updates, and compliance with local Health Authority requirements. • Collaborate with global and local teams to provide regulatory input during product development, launch planning, and marketing campaigns. • Monitor regulatory legislation, marketing applications, and submissions to ensure timely approvals. • Liaise and negotiate with authorities to secure regulatory approvals efficiently. • Review and approve labeling, advertising, and promotional materials for compliance. • Support cross-functional teams with regulatory documentation, such as Market Standing Certificates, GMP, Manufacturing Licenses, and other regulatory certificates. • Ensure compliance with internal processes, company policies, and local regulatory requirements. Qualification: • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related field. Experience: • Experience in new drug registration, clinical trials, and regulatory submissions in India. • Exposure to cross-functional collaboration with RA, Medical Affairs, Marketing, Quality, and Global Regulatory teams. Skills: • Strong knowledge of regulatory affairs processes, local regulations, and Health Authority requirements. • Excellent communication, negotiation, and interpersonal skills. • Project management skills and ability to work in a fast-paced environment. • Analytical and problem-solving abilities. • Domain knowledge of subregion country regulations is a plus. About the Organisation: Domnic Lewis Pvt. Ltd is a leading healthcare and pharmaceutical company focused on delivering high-quality, compliant solutions across India and international markets, emphasizing innovation, regulatory excellence, and cross-functional collaboration.

Roles & Responsibilities: • Manage administrative tasks for non-linguistic Pharmacovigilance (PV) projects, including file transfers, internal process checks, and client deliverables. • Monitor project progress, communicate updates, and ensure strict adherence to deadlines. • Uphold Good Pharmacovigilance Practices (GVP) and Good Documentation Practice in all projects. • Support the Production team in day-to-day project coordination. • Complete tasks assigned by managers or supervisors. Qualification: • Minimum Bachelor’s degree. Experience: • Prior experience in project coordination or administrative support is a plus. • Exposure to pharmaceutical, healthcare, or PV-related environments is advantageous. Skills: • Superior written and spoken English communication. • Proficiency in Microsoft Office (Word, Excel, Outlook). • Quick learner with aptitude for various technology platforms. • Strong problem-solving and critical thinking skills. • Excellent attention to detail and organizational skills. • Ability to multitask in a fast-paced environment. • Can work independently or as part of a team. • Strong interpersonal skills and ability to collaborate with diverse teams. About the Organisation: TransPerfect is a global leader in language and technology solutions, providing translation, localization, and compliance support across industries such as healthcare, life sciences, and legal, with a focus on quality, innovation, and client satisfaction, offering opportunities for professional growth in a multicultural work environment.

Roles & Responsibilities: • Research, write, and review scientific response documents under the guidance of the Global Medical Information (GMI) team • Conduct comprehensive literature searches and extract, analyze, and summarize complex scientific data • Develop accurate, evidence-based, current, and fair-balanced medical information responses for assigned therapeutic areas • Adapt global medical information documents for local and regional markets • Prepare responses to escalated medical inquiries for supported countries • Contribute to US NDA Annual Reports and US compendia reviews • Participate in peer reviews and review content created by other medical writers • Collaborate closely with Global Medical Information, Pharmacovigilance, and Medical Affairs teams • Maintain and continuously enhance therapeutic area expertise • Support cross-functional projects and ensure timely delivery of assigned deliverables • Assist other medical information writers through knowledge sharing and mentoring • Ensure compliance with global and local regulatory requirements related to medical information Qualification: • Advanced degree in Life Sciences, Pharmacy, or related discipline • Medical degree or doctorate preferred (PharmD, PhD, MSc, MBA or equivalent) Experience: • More than 5 years of experience in medical writing within the pharmaceutical or healthcare industry or equivalent clinical experience • Minimum 2–3 years of direct Medical Information experience in a pharmaceutical company Skills: • Strong scientific and medical writing and editing skills • Expertise in literature evaluation and evidence-based content development • Excellent stakeholder management and cross-functional collaboration skills • Strong time management, risk management, and operational excellence abilities • Ability to work independently and in a team-oriented environment • High attention to detail and commitment to quality and timelines • Excellent written and spoken English proficiency About the Organisation: Sanofi Business Operations (SBO) is Sanofi’s global capability center in India, supporting Medical, Commercial, HEVA, R&D, and Digital functions worldwide. SBO plays a strategic role in delivering high-quality scientific, medical, and operational support across Sanofi’s Specialty Care, Vaccines, General Medicines, and Consumer Healthcare portfolios, helping advance patient care through innovation, collaboration, and scientific excellence.

Roles & Responsibilities: • Deliver high-quality, patient-centric healthcare services in line with Apollo Hospitals’ clinical and ethical standards • Collaborate with multidisciplinary medical teams to ensure effective diagnosis, treatment, and patient care • Utilize advanced medical technologies and hospital infrastructure to support accurate and timely healthcare delivery • Maintain patient safety, confidentiality, and compliance with hospital protocols and regulatory guidelines • Participate in continuous learning, quality improvement, and innovation initiatives • Support preventive healthcare, wellness programs, and community outreach activities Qualification: • Relevant educational qualifications as per the specific clinical or healthcare role • Certification and professional registration as applicable Skills: • Strong patient-care orientation and ethical medical practice • Effective communication and teamwork abilities • Adaptability to advanced healthcare technologies and systems • Commitment to continuous learning and quality improvement • Compassion, integrity, and professionalism About the Organisation: Apollo Hospitals is one of India’s most trusted and established healthcare providers, known for its state-of-the-art medical facilities, advanced technology, and highly skilled healthcare professionals. With a strong focus on patient-centric care, innovation, research, and social responsibility, Apollo Hospitals delivers comprehensive healthcare services across multiple specialties while promoting preventive care, wellness, and community health initiatives.

Roles & Responsibilities: • Dispense prescribed medications accurately and in a timely manner • Review prescriptions to ensure correctness, safety, and compliance • Provide clear guidance and counseling to patients on medication usage, dosage, and potential side effects • Maintain accurate records of prescriptions, inventory, and patient information • Ensure adherence to pharmacy regulations, safety standards, and internal procedures • Deliver high-quality customer service and support during overnight operations Qualification: • Bachelor’s degree in Pharmacy (B.Pharm) or equivalent from a recognized institution Experience: • Relevant experience as a Pharmacist preferred (freshers with strong knowledge may be considered) Skills: • Strong knowledge of pharmaceuticals, medication management, and prescription processing • Excellent customer service and patient counseling skills • High attention to detail with strong problem-solving abilities • Ability to maintain accurate records and handle responsibilities independently • Good communication skills and professional approach About the Organisation: Chehab Pharmacy is a trusted community pharmacy committed to delivering safe, reliable, and patient-focused pharmaceutical care. The organization emphasizes professional ethics, customer satisfaction, and continuous service excellence to support community health needs.

Roles & Responsibilities: • Lead, coach, and develop a team of Health Representatives (HRs) in line with Pfizer’s competency model • Enhance customer experience and drive effective HCP engagement through scientific, educational, and promotional activities • Achieve assigned financial, sales, and operational objectives for the business area and territories • Drive market share growth and strengthen brand image for assigned products • Develop and implement territory and activity plans with cross-functional alignment • Coach HRs on best-in-class scientific promotion to support informed treatment decisions by HCPs • Set brand and financial objectives and monitor execution and performance • Conduct regular performance reviews, appraisals, and capability-building initiatives • Identify talent, address performance gaps, and support long-term development and retention • Build and maintain strong professional relationships with HCPs and key stakeholders • Ensure compliance with company policies, procedures, and effective use of resources • Support annual budgeting, forecasting, and reporting of promotional and engagement activities • Track, analyze, and report business and team performance metrics Qualification: • Bachelor’s degree in Pharmacy or Medicine Experience: • Minimum 7 years of commercial experience in the pharmaceutical industry • Mandatory Gulf experience (preferably across multiple markets) • Vaccines experience highly preferred Skills: • Strong leadership, coaching, and people management capabilities • Excellent business acumen and strategic thinking • Ability to manage complex situations and cross-functional collaboration • Strong analytical, influencing, and decision-making skills • Entrepreneurial mindset with a focus on growth and performance • In-depth understanding of healthcare systems and market dynamics • Excellent written and verbal communication skills in English and Arabic • Strong presentation and stakeholder engagement skills • Role model for company values and ethical behavior About the Organisation: Pfizer is a global biopharmaceutical leader committed to delivering breakthroughs that change patients’ lives. With a strong focus on science, innovation, and values-driven leadership, Pfizer empowers its teams to advance healthcare, strengthen trust with healthcare professionals, and make a meaningful impact across global and regional markets.

Roles & Responsibilities: • Promote nutraceutical products under the OTRX line across Pharmacy and HCA channels • Build and maintain strong professional relationships with pharmacists, healthcare professionals, and key accounts • Achieve assigned sales targets and expand market presence within the allocated territory • Plan and execute regular field visits to pharmacies and healthcare accounts • Manage territory independently with effective coverage and follow-ups • Ensure ethical promotion and accurate product communication • Monitor market trends, competitor activity, and customer feedback • Maintain proper sales records and reporting as per company guidelines Qualification: • Bachelor’s degree or equivalent in Pharmacy, Veterinary Medicine, or Science Experience: • Minimum 2 years of relevant experience in nutraceutical or healthcare product sales Skills: • Strong communication, negotiation, and interpersonal skills • Proven ability to manage territories and meet sales objectives independently • Knowledge of nutraceutical products and pharmacy/HCA sales channels • Professional attitude with strong ethical standards • Valid UAE driving license (mandatory) About the Organisation: United Pharma is a growing healthcare company focused on delivering high-quality nutraceutical and healthcare solutions across the UAE. With a strong presence in pharmacy and healthcare channels, the company emphasizes ethical promotion, innovation, and long-term partnerships to improve health outcomes and strengthen its market leadership.

Roles & Responsibilities: • Develop and execute territory sales plans in collaboration with sales managers • Achieve or exceed sales targets while effectively managing assigned budgets • Implement AstraZeneca’s marketing and medical promotion strategies across products and regions • Conduct regular, high-quality medical visits aligned with approved visit plans and objectives • Promote products through scientific, ethical, and customized communication to healthcare professionals • Maintain accurate records of customer interactions and activities using CRM tools (e.g., Veeva) • Organize and manage promotional meetings such as RLMs and ROMs with efficient budget utilization • Monitor competitor activities and local market trends to optimize product positioning • Coordinate with internal teams including Medical, Pharmacovigilance, Marketing, and Regulatory • Build and sustain strong, ethical relationships with healthcare professionals • Continuously update product, therapeutic, and market knowledge through training and self-learning • Ensure full compliance with industry regulations and company policies Qualification: • Bachelor’s degree in Pharmacy, Medicine, Life Sciences, or a related discipline Experience: • 1–2 years of experience as a Medical Representative in the pharmaceutical industry Skills: • Strong scientific and ethical medical promotion knowledge • Excellent communication, presentation, and interpersonal skills • Ability to analyse sales and market data and develop action plans • Proficiency in CRM tools such as Veeva and reporting systems • Strong planning, organizational, and territory management skills • Ability to work effectively in a fast-paced, dynamic environment • Strong cross-functional collaboration skills • Fluency in French and Arabic (mandatory); English proficiency is a strong advantage About the Organisation: AstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialization of innovative medicines for serious diseases. Driven by strong scientific expertise and ethical values, the company is committed to improving patient outcomes, advancing healthcare, and fostering a culture of continuous learning, collaboration, and professional excellence worldwide.

Roles & Responsibilities: • Develop and execute territory sales plans in coordination with sales managers • Achieve or exceed sales targets and manage allocated budgets effectively • Conduct high-quality medical visits aligned with approved visit plans • Promote products scientifically, ethically, and in compliance with regulations • Organize and manage promotional meetings (RLMs, ROMs) • Maintain accurate records of interactions and activities using CRM tools (e.g., Veeva) • Monitor competitor activities and local market dynamics • Collaborate with internal teams (Medical, Marketing, PV, Regulatory) • Build and maintain strong, ethical relationships with healthcare professionals • Continuously update product, therapeutic, and market knowledge • Ensure strict adherence to company policies and industry regulations Eligibility & Qualifications: • Bachelor’s degree in Pharmacy, Medicine, Life Sciences, or related field • 1–2 years’ experience as a Pharmacy Representative in the pharma industry • Strong understanding of medical promotion practices and ethical guidelines • Ability to analyse sales data and implement targeted action plansSkills: • Strong communication, presentation, and interpersonal abilities • Good analytical skills to interpret sales and market data • Proficiency in CRM tools such as Veeva • Strong planning, organization, and time-management skills • Adaptability in a dynamic, fast-paced environment • Language proficiency in French and Arabic (mandatory); English is an added advantageAbout the Organisation: AstraZeneca is a global, science-led, patient-focused biopharmaceutical company engaged in the discovery, development, and commercialization of innovative prescription medicines for some of the world’s most serious diseases. With a strong commitment to ethics, scientific excellence, and continuous learning, AstraZeneca empowers its people to make a meaningful impact on patients, healthcare systems, and society worldwide.

Roles & Responsibilities: • Provide expert pharmaceutical consultation to patients and healthcare professionals • Counsel patients on medication usage, dosage, interactions, and possible side effects • Implement and maintain pharmacy quality assurance programs in line with MOH standards • Ensure compliance with regulatory, safety, and confidentiality requirements • Maintain accurate patient records using pharmacy systems and electronic health records • Stay updated with new drug approvals, treatment guidelines, and best pharmacy practices • Participate in public health initiatives and medication safety education programs • Support continuous improvement in pharmacy operations and patient care Qualification: • B.Pharm or M.Pharm from a recognized institution • Valid pharmacy license with eligibility for MOH licensure Experience: • Minimum 2 years of experience in a hospital or community pharmacy in the UAE Skills: • Strong communication and interpersonal skills • Proficiency in pharmacy information systems and EHRs • Ability to work independently and in a team environment • Problem-solving and decision-making skills • Fluency in English; Arabic proficiency highly desirable • Willingness to relocate to Ras Al Khaimah About the Organization: ENZO GENERAL TRADING LLC OPC operates in the healthcare and pharmaceutical sector, focusing on quality-driven pharmacy services and compliance with UAE MOH standards to ensure safe and effective patient care.

Roles & Responsibilities: • Promote and sell medical devices to doctors, clinics, and hospitals • Build and maintain strong relationships with healthcare professionals and key decision-makers • Conduct product demonstrations, presentations, and training sessions • Achieve assigned monthly and quarterly sales targets • Provide after-sales support and ensure customer satisfaction • Generate and track leads, sales activities, and customer interactions using CRM tools • Monitor competitor activities and market trends • Coordinate with marketing teams for lead generation and brand visibility • Travel within the assigned territory as required Qualification: • Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, or related discipline (preferred) Experience: • 1–3 years of experience in medical device sales or pharmaceutical sales Skills: • Strong communication and negotiation skills • Relationship-building and presentation skills • Customer-focused and target-driven approach • Basic CRM and reporting knowledge About the Organization: The Aligner Company is a fast-growing healthcare technology organization specializing in innovative medical device solutions, offering strong career growth, structured training, and performance-based incentives in the medical devices sector.

Roles & Responsibilities: • Manage and develop existing and new key accounts and government business at zonal level for IVD instruments and reagents • Drive sales growth, forecasting monthly and annual targets with profitability accountability • Handle key account management, customer relationship management, satisfaction, and retention • Analyze key account performance and market share, prepare corrective action plans • Align with zonal teams and cascade business strategies for growth • Generate leads, negotiate, and successfully close deals • Coordinate with customers and internal teams for timely delivery and payment collection • Conduct periodic reviews with government and key institutional customers • Execute innovative promotional activities, roadshows, CMEs, and product demonstrations • Monitor market trends, competition, and submit regular reports, DCRs, and MIS on TAB • Ensure compliance with company systems, processes, and ethical sales practices Qualification: • BE / B.Tech / B.Sc / M.Sc / B.Pharm / Diploma Experience Required: • 2–5 years of Key Account and Government Business experience in the IVD industry Skills: • Key account & govt. business handling • Strategic sales planning & forecasting • Negotiation & relationship management • Market analysis & reporting • Strong communication and leadership skills About the Organization: Erba Transasia is a leading in-vitro diagnostics company offering comprehensive diagnostic solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics, with a strong presence in India and global markets.

Roles & Responsibilities: • Promote assigned IVD (in-vitro diagnostics) products to customers at defined frequencies. • Generate leads and convert opportunities into sales. • Coordinate with customers, credit control, and internal teams for timely and outstanding payment collections. • Build and maintain strong relationships with customers and distributors. • Ensure compliance with company systems, policies, and sales processes. • Negotiate effectively and close sales deals successfully. • Ensure timely and accurate delivery of products to customers. • Monitor market trends, competitor activities, and product performance and report insights to management. • Prepare daily call reports, update attendance, capture product complaints, and record opportunities using the TAB system. • Submit Field Expense Statements (FES) within stipulated timelines. • Support roadshows, CMEs, and product demonstrations. • Continuously update technical knowledge and selling skills. Qualification: • B.Sc / B.Pharm / B.Tech / B.E / Diploma. Experience: • Minimum 2 years of experience in IVD Government Sales. Skills: • Strong sales, negotiation, and relationship-building skills. • Good understanding of IVD products and government sales processes. • Ability to coordinate with multiple stakeholders and internal teams. • Strong communication, reporting, and documentation skills. • Willingness to travel extensively within the assigned territory. About the Organization: Erba Transasia is a leading diagnostics company with a strong presence in India and global markets, offering a comprehensive range of in-vitro diagnostic solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics. Known for innovation, quality, and customer-centric solutions, Erba Transasia supports healthcare providers with reliable diagnostic technologies.

Roles & Responsibilities: • Lead development and optimization of immunoassays based on fluorescence and chemiluminescence techniques. • Perform assay verification, validation, and robustness studies as per regulatory and quality requirements. • Support process transfer from R&D to manufacturing and ensure scale-up readiness. • Design, execute, and document experimental studies for immunoassay development. • Analyze data, troubleshoot assay issues, and implement improvements. • Prepare technical documentation, validation reports, and development summaries. • Collaborate with cross-functional teams including manufacturing, QA, and regulatory. • Ensure compliance with applicable quality systems and laboratory standards. Qualification: • M.Sc / M.Tech / PhD in Life Sciences or related disciplines. Experience: • 5–8 years of experience in development and optimization of immunoassays. • Hands-on exposure to fluorescence and/or chemiluminescence-based assay platforms. Skills: • Strong expertise in immunoassay development and validation. • Experience with assay verification, method validation, and process transfer. • Sound understanding of analytical techniques and data interpretation. • Strong documentation, problem-solving, and cross-functional coordination skills. • Ability to work independently in an R&D-driven diagnostic environment. About the Organization: Erba Mannheim Transasia is a global diagnostics leader and one of India’s largest diagnostic companies, delivering innovative solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics. With a strong focus on research, quality, and advanced technology, the organization plays a key role in shaping the future of diagnostics worldwide.

Roles & Responsibilities: Analytical Development Laboratory (ADL): • Perform routine analysis and analytical method development for solid orals, injectables, semi-solids, liquids, oral liquids, and APIs. • Execute analytical method validation, verification, and transfer including protocol and report preparation. • Independently handle HPLC, UV Spectrophotometer, and dissolution apparatus for assay, content uniformity, blend uniformity, dissolution, and related substances testing. Formulation & Development (F&D): • Develop formulations for solids, semi-solids, injectables, and oral liquids. • Conduct product development, stability studies, and scale-up activities in a GMP environment. • Support technology transfer and process optimization. Packaging Development: • Perform packaging material selection, development, and testing for pharmaceutical products. • Ensure packaging compliance with regulatory requirements for different dosage forms. • Support stability, compatibility, and packaging validation activities. Qualification: • ADL: M.Sc / B.Pharm / M.Pharm • F&D: M.Pharm • Packaging Development: B.Pharm / M.Pharm (Diploma/Certification preferred) Experience: • For ADL: 2–12 years • For F&D: 3–10 years • For Packaging Development: 3–10 years Skills: • Strong knowledge of GMP, analytical techniques, and pharmaceutical development processes. • Hands-on experience in formulation, analytical validation, or packaging development. • Good documentation, compliance, and cross-functional coordination skills.Walk-In Interview Details: Date: 1st February 2026 (Sunday) Time: 9:00 AM – 3:00 PM Venue: LINCOLN HOUSE, Behind Satyam Complex, Science City Road, Sola, Ahmedabad – 380060, Gujarat Documents to Carry: • Updated resume • Educational certificates • Experience letters • Relevant supporting documents About the Organization: Lincoln Pharmaceuticals Ltd is a WHO-GMP and ISO-certified pharmaceutical company based in Ahmedabad, focused on delivering affordable and innovative healthcare solutions with a strong presence across domestic and international markets.

Roles & Responsibilities: • Coordinate with Sponsors and internal Operations teams for clinical trial feasibility with quick turnaround times. • Oversee ethical conduct of Phase II–IV clinical trials in compliance with ICH-GCP and regulatory standards. • Ensure timely completion of clinical trials with high-quality, error-free data collection from sites. • Drive repeat business from Sponsors/CROs through superior site performance and delivery. • Train and mentor operations teams on essential clinical trial documents and ethical trial conduct. • Lead recruitment, capacity building, and performance development of the clinical operations team. • Handhold teams throughout the entire clinical trial lifecycle and identify high performers for vertical growth. • Prepare sites for FDA audits and ensure audit readiness. • Develop new clinical trial sites across India, including non-metro locations, and build therapeutic area–specific investigator networks. • Establish and implement SOPs, operational systems, controls, and efficient marketing processes. • Prepare business plans, achieve targets, and continuously improve operational and marketing strategies. • Anticipate risks, mitigate issues proactively, and ensure adherence to sponsor timelines. • Monitor market trends, gather industry intelligence, and keep management informed. • Prepare MIS and management reports and maintain strict control on headcount. Qualification: • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or related field. Experience: • Extensive experience in clinical operations with strong exposure to Phase II–IV clinical trials and site management. Skills: • Strong leadership and team-building capabilities. • Excellent sponsor and stakeholder management skills. • Deep understanding of clinical trial operations, ethics, and regulatory compliance. • Strategic planning, risk management, and business development skills. • Ability to work across metro and non-metro clinical trial sites. • Strong communication, training, and reporting skills. About the Organization: The organization operates in the clinical research domain with a focus on ethical, high-quality clinical trial execution across India. It emphasizes operational excellence, regulatory compliance, strong investigator networks, and sustainable growth through robust systems, processes, and team development.

Roles & Responsibilities: • Perform method validation and method verification for drug substance (DS), drug product (DP), and in-process samples. • Conduct stability studies, IRS qualification, and biosimilarity assessments. • Prepare and review controlled documents including specifications, STPs, SOPs, TDS, COAs, MVPs/MVRs, and MTRs. • Coordinate with vendors for external calibration and support in-house calibration activities. • Manage validation lab inventory, chemicals, standards, kits, and consumables. • Maintain laboratory instruments, equipment, and usage logbooks. • Conduct analyst qualification and training for validation lab team members. • Initiate and track QMS activities, deviations, and investigations. • Ensure cGMP compliance and adherence to laboratory safety requirements. • Support additional tasks assigned by the reporting manager. Qualification: • M.Sc / M.Pharm / Master’s degree in Biotechnology or related life science disciplines. Experience: • 2–5 years of hands-on experience in analytical validation laboratories (biologics/biosimilars preferred). Skills: • Strong hands-on experience with CEX-HPLC, SE-HPLC, ELISA, RT-PCR (HCDNA), Maurice, SOLO VPE. • Experience in HCP analysis, peptide mapping, glycan analysis, and capillary electrophoresis. • Knowledge of stability studies, method validation, and biosimilarity testing. • Sound understanding of cGMP, QMS, and laboratory compliance requirements. • Strong documentation, coordination, and analytical skills. About the Organization: Enzene Biosciences is a biopharmaceutical company focused on the development and manufacturing of biologics and biosimilars for global markets. With advanced analytical and validation laboratories, Enzene offers professionals the opportunity to work with cutting-edge technologies while building expertise in GMP-regulated biopharmaceutical quality and validation operations.

Roles & Responsibilities: • Lead authoring and review of aggregate safety reports (PSUR/PBRER, DSUR, PADER, Annual Reports). • Prepare benefit–risk evaluations, signal detection reports, and ad hoc regulatory safety documents. • Author and review RMPs, safety update reports, addendum reports, and CTD summaries (Clinical & Non-Clinical Overviews, Clinical Summaries). • Develop and update product labeling documents (CDS, USPI, SmPC/SPC, Medication Guides). • Conduct scientific literature reviews, recommend label updates, and prepare justification documents. • Generate and review line listings, summary tabulations, CFIs, and CFCs. • Prepare medical information responses for healthcare professionals (HCPs). • Coordinate safety writing projects including resource planning, timelines, and cross-functional communication. • Act as primary client contact for safety writing deliverables and ensure quality, compliance, and audit readiness. • Support RFPs, resource estimation, metrics tracking, and mentor junior writers. Qualification: • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field (Master’s/PhD preferred). Experience: • 5–7 years of experience in the pharmaceutical industry or minimum 4 years in medical/safety writing. Skills: • Strong expertise in pharmacovigilance regulations, ICH guidelines, and aggregate safety reporting. • Excellent scientific writing and communication skills. • Proficiency in MS Office and strong project coordination abilities. • Client-facing, leadership, and mentoring skills. • In-depth understanding of disease areas, drug safety lifecycle, and risk management. About the Organization: Fortrea is a global clinical development and pharmacovigilance services company supporting pharmaceutical and biotech organizations worldwide. With a strong focus on scientific excellence, regulatory compliance, and patient safety, Fortrea offers professionals the opportunity to lead complex global safety projects in a collaborative and growth-driven environment.