Pharma Jobs

WhatsApp Group Join Now Instagram Group Join Now Aurigene Pharmaceutical Services Limited is hiring a Team Leader – Process R&D in Hyderabad, Telangana. This senior leadership role is ideal for highly experienced professionals with a strong background in organic chemistry, process development, and scale-up operations within the pharmaceutical industry. Join a dynamic team focused on driving quality, innovation, and scientific excellence in process research and development. Company Overview Aurigene Pharmaceutical Services Limited is a leading pharmaceutical CDMO (Contract Development & Manufacturing Organization) recognized for delivering high-quality chemical processes and development services. The company supports clients across drug discovery and early-stage process R&D, delivering robust and scalable solutions for complex molecules. Job Summary As the Team Leader – Process R&D, you will lead process design, development, optimization and scale-up projects, ensuring scientific rigor, safety, and delivery excellence. Key Responsibilities As a Process R&D Team Leader, your responsibilities include: This role demands technical leadership, scientific excellence, and the ability to drive multiple R&D initiatives from concept to execution. Required Qualifications & Experience To succeed in this role you should have: This senior position is tailored for experienced hands with strong scientific leadership and operational rigor. Why This Opportunity is Exciting Joining Aurigene as Team Leader – Process R&D offers: Aurigene values scientific excellence and team leadership, making this role ideal for visionary professionals seeking growth. How to Apply For apply this opportunity CLICK HERE

WhatsApp Group Join Now Instagram Group Join Now Aculife Healthcare Pvt Ltd, a part of the Nirma Group, is conducting a walk-in interview on 30 January 2026 for Production, QA, QC, and ADL positions. This is an excellent opportunity for freshers and experienced candidates from science and pharmacy backgrounds to join a reputed pharmaceutical organization. Candidates with qualifications in B.Sc, M.Sc, B.Pharm, or M.Pharm are encouraged to attend the walk-in interview. Company Overview – Aculife Healthcare Pvt Ltd Aculife Healthcare Pvt Ltd is a leading pharmaceutical company specializing in parenteral and injectable formulations. Known for its strong compliance culture and quality-driven manufacturing, Aculife operates under the Nirma Group, offering long-term career growth and learning opportunities. Walk-In Interview Details Job Openings at Aculife Healthcare 1. Production Department Eligibility: Key Experience Required: 2. Quality Assurance (QA) Eligibility: Key Experience Required: 3. Quality Control (QC) Eligibility: Key Experience Required: 4. ADL – Analytical Development Laboratory Eligibility: Key Skills Required: Additional Open Positions Interview Venue Aculife Healthcare Private Limited(Formally known as “Inlife”)Near Railway Crossing, Sanand–Viramgam HighwayVillage: SachanaTaluka: ViramgamDistrict: Ahmedabad – 382150 How to Apply Interested candidates can attend the walk-in interview directly or share their resume via email: Carry updated resume, passport-size photograph, and relevant documents.

WhatsApp Group Join Now Instagram Group Join Now SVAK Life Sciences is hiring a Research Associate – Synthesis R&D at its Hyderabad facility. This is a great opportunity for chemistry and pharmacy professionals who want to grow their career in synthetic research and development within a fast-growing life sciences organization. If you have hands-on experience in chemical synthesis, reaction monitoring, purification, and lab documentation, this role could be the perfect next step in your career. Job Overview Key Responsibilities As a Research Associate in Synthesis R&D, you will be responsible for: Required Qualifications & Experience To apply for this Research Associate – Synthesis R&D job in Hyderabad, candidates should have: Why Join SVAK Life Sciences? How to Apply Interested candidates can apply directly using the contact details below: 📩 Mention “Research Associate – Synthesis R&D” in the subject line for faster processing.

WhatsApp Group Join Now Instagram Group Join Now Are you a skilled microbiology professional with hands-on lab experience? Vitaliz Biosciences Pvt Ltd is hiring a Microbiologist in Thiruvananthapuram, Kerala — a full-time role ideal for candidates with 3–5 years of microbiology experience in culture handling, analysis, and quality assurance. About Vitaliz Biosciences Pvt Ltd Vitaliz Biosciences is a specialty nutrient and bioscience company based in Thiruvananthapuram that focuses on essential fatty acids, fortified probiotics, and other functional ingredients for food and nutraceutical sectors. Job Summary – Microbiologist As a Microbiologist, you will conduct routine and specialized microbiological tasks to support product quality, contamination control, and laboratory operations in a production environment. Key Responsibilities Your daily responsibilities will include: This role emphasizes thorough lab practices, careful handling of cultures, and proper record-keeping to uphold quality standards. Required Skills & Qualifications To be successful in this role, you should have: ✔ Education: M.Sc. in Microbiology, Biotechnology, Life Sciences or equivalent.✔ Experience: Around 3–5 years in a microbiology laboratory.✔ Strong knowledge of microbial culturing, sterilization, and aseptic techniques.✔ Ability to maintain laboratory equipment and prepare solutions accurately.✔ Excellent documentation, analytical, and teamwork skills.✔ Detail-oriented approach to ensure quality and contamination control. Why This Job Matters Working as a Microbiologist at Vitaliz Biosciences offers you a chance to apply your technical skills in a lab-based role with real impact on product quality and research workflows. You’ll gain experience in culture preparation, microbial testing, and inter-department collaboration — valuable for growth in bioscience and quality assurance careers. How to Apply Interested candidates should apply through the CLICK HERE

WhatsApp Group Join Now Instagram Group Join Now Are you a biotechnology graduate looking for a pharma job in Hyderabad? Here’s a great opportunity to start your career with MSN Group as a Biotechnology Executive at their Rudraram facility in Telangana. This role is suitable for freshers and early-career professionals with a background in biotechnology seeking hands-on experience in industrial biotech operations. About MSN Group MSN Group is a reputed pharmaceutical and biotech organization headquartered in Hyderabad, Telangana, known for its state-of-the-art biologics, fermentation, and manufacturing operations. The company operates globally and focuses on innovation, quality, and compliance with regulatory standards. Job Summary – Biotechnology Executive This MSN Group biotechnology executive job offers entry-level professionals the chance to grow in a dynamic biotech and pharma environment. Key Responsibilities As a Biotechnology Executive, your day-to-day work will include: This hands-on experience will help you build practical biotechnology and manufacturing skills. Required Qualifications & Skills To apply for this MSN Group biotechnology executive job, you should have: Freshers and candidates with up to 3 years of experience are encouraged to apply. Job Location 📍 Rudraram, Sangareddy, Hyderabad, Telangana – a thriving industrial hub for pharmaceuticals and biotechnology in India. Why Join MSN Group? Joining MSN Group as a Biotechnology Executive provides: ✨ A strong foundation in industrial biotech operations✨ Exposure to advanced fermentation and process development✨ Career growth opportunities within a global pharmaceutical company✨ Hands-on work in R&D and production environments This role is perfect for biotech professionals eager to kickstart their career in the pharmaceutical and biotech manufacturing sector. How to Apply CLICK HERE

WhatsApp Group Join Now Instagram Group Join Now Are you passionate about genomics, DNA sequence analysis, and precision diagnostics? MedGenome Labs Ltd., a leader in genetic testing and research services, is hiring a Genome Analyst in Bengaluru, Karnataka, India — ideal for early-career professionals in life sciences and genetics. About the Company — MedGenome Labs MedGenome Labs Ltd. is one of India’s foremost genomics research and diagnostics companies, operating South Asia’s largest CAP-accredited genomics laboratory. The company is known for its advanced Next-Generation Sequencing (NGS) services and multi-omics solutions that support clinical diagnostics, research, and personalized medicine initiatives. Job Summary — Genome Analyst Location: Bengaluru, Karnataka, IndiaCompany: MedGenome Labs Ltd.Job Type: Full-timeExperience: 0–2 years (entry level)Industry: Genomics, Molecular Diagnostics As a Genome Analyst, you’ll work with sequencing data and help produce clinically relevant insights by interpreting genomic data and supporting laboratory research operations. Training and guidance are typically provided to help you succeed. Key Responsibilities As a Genome Analyst at MedGenome Labs, your core duties will include: These responsibilities help ensure accurate, scientifically valid reports for genetic diagnostics and research activities. Required Skills & Qualifications To qualify for this role, ideal candidates should have: ✔ Education: M.Sc. or equivalent in Life Sciences, Genetics, Biotechnology, Molecular Biology, or related field.✔ Experience: 0–2 years of relevant genomics or laboratory experience (freshers welcome in some cases).✔ Familiarity with NGS data interpretation and variant analysis.✔ Strong analytical thinking and attention to detail.✔ Excellent communication and documentation skills. This role is great for early-career scientists who want to build expertise in genomic diagnostics and clinical research. Why Join MedGenome Labs Working at MedGenome offers: ✨ Exposure to cutting-edge NGS and genomics technologies.✨ Opportunity to contribute to diagnostics and research impacting healthcare outcomes.✨ Collaboration with experienced research and bioinformatics professionals. This is an excellent entry point for scientists aiming to grow in genomic data analysis and molecular diagnostics. How to Apply To apply for the Genome Analyst job at MedGenome Labs, CLICK HERE

WhatsApp Group Join Now Instagram Group Join Now Are you a research professional with a strong background in ADME, DMPK, and bioanalytical techniques? Eurofins IT Solutions India Pvt Ltd is hiring an Associate Research Scientist – DMPK in Bengaluru, Karnataka, India. This position offers an exciting opportunity to work in drug metabolism and pharmacokinetics research within a global pre-clinical contract research organization (CRO). Company Overview Eurofins IT Solutions India Pvt Ltd is part of the Eurofins Scientific group — one of the world’s largest networks of analytical testing laboratories serving pharmaceutical, biotech, and CRO sectors. Known for its high-quality ADME and DMPK research services, Eurofins provides robust support for early drug discovery and development projects globally. Job Summary: Associate Research Scientist – DMPK Location: Bengaluru, Karnataka, IndiaEmployment Type: Full-timeDepartment: DMPK (Drug Metabolism & Pharmacokinetics) As an Associate Research Scientist – DMPK, you’ll be responsible for conducting specialized in-vitro ADME studies, bioanalytical workflows, and ensuring data integrity during drug metabolism research. This role is ideal for early-to-mid career scientists ready to contribute to impactful preclinical research. Key Responsibilities In this role, you will typically: Required Qualifications & Skills To be eligible for this role, candidates should have: ✔ Education: Master’s degree in Pharmacy / Biotechnology / Chemistry / Biochemistry or related life sciences field.✔ Experience: 1-4 years of relevant experience in DMPK, ADME, or bioanalytical research.✔ Practical skills in LC-MS/MS data acquisition and analysis.✔ Strong analytical thinking, scientific reporting, and teamwork skills. This role is ideal for life sciences graduates with hands-on laboratory experience who want to grow their career in pharmaceutical research. FOR APPLY CKICK HERE

WhatsApp Group Join Now Instagram Group Join Now If you are looking for a leadership role in regulatory affairs within the pharmaceutical sector, this Azurity Pharmaceuticals job vacancy in Hyderabad could be an excellent opportunity. The company is actively hiring for the position of Manager, Regulatory Affairs, offering a strategic role in global regulatory submissions, life-cycle management, and compliance. About Azurity Pharmaceuticals Azurity Pharmaceuticals is a specialty pharmaceutical company focused on developing innovative dosage forms for underserved patient populations. It leverages its integrated commercial, scientific, and regulatory expertise to deliver high-quality medications across multiple therapeutic areas such as cardiovascular, endocrinology, neurology, and gastrointestinal care. With a strong commitment to quality and patient-centric products, Azurity provides a professional environment that supports innovation, team collaboration, and meaningful career growth. Job Summary – Manager, Regulatory Affairs As Manager of Regulatory Affairs, you’ll play a crucial role in coordinating and executing regulatory strategies to support product registrations and ongoing compliance across markets. Azurity Pharmaceuticals job vacancy in Hyderabad Key Responsibilities In this role, you will be responsible for: This position is ideal for candidates with strong regulatory experience and strategic thinking skills in the pharmaceutical field. Azurity Pharmaceuticals job vacancy in Hyderabad Required Skills & Qualifications Successful applicants should possess: Azurity Pharmaceuticals job vacancy in Hyderabad Job Location 📍 Hyderabad, Telangana, India – a major hub for pharmaceutical and biotechnology industries in India. Why Join Azurity Pharmaceuticals? Working in this managerial role at Azurity offers: ✨ A leadership position with strategic influence✨ Exposure to international regulatory procedures and frameworks✨ Collaboration with scientific, commercial, and quality assurance teams✨ Career growth and development in a fast-growing pharma company This role is perfect for experienced regulatory professionals who want to make a meaningful impact in product approvals and global health outcomes. Azurity Pharmaceuticals job vacancy in Hyderabad How to Apply

WhatsApp Group Join Now Instagram Group Join Now Are you a qualified medical professional looking for a rewarding opportunity in clinical review and healthcare operations? MSN Laboratories is hiring a Medical Officer in Hyderabad, Telangana, India — a vital role for doctors passionate about medical safety and regulatory review. Company Overview — MSN Laboratories MSN Laboratories is a pharmaceutical and healthcare company involved in manufacturing, quality assurance, and clinical services. With a focus on patient safety and high-quality healthcare solutions, MSN places importance on professionals who can uphold medical standards in review and compliance. The Medical Officer position at MSN offers a strong platform for clinicians interested in bridging medical practice with pharmaceutical regulatory work. Job Summary — Medical Officer Location: Hyderabad, Telangana, IndiaCompany: MSN LaboratoriesEmployment Type: Full-timeSeniority Level: AssociateIndustry: Pharmaceutical Manufacturing, HealthcareExperience: Doctorate (MBBS/MD) preferred (based on job description) The Medical Officer will play a key role in medical review functions within the organization — ensuring safety, quality, and compliance of regulatory documentation. Key Responsibilities As a Medical Officer at MSN Laboratories, your duties may include: This role is especially suited for medically qualified professionals with strong analytical skills and a detail-oriented approach to clinical documentation and reporting. Qualifications & Skills Required To succeed in this role at MSN Laboratories, candidates should ideally have: ✔ MBBS or MD degree (in Pharmacology or related clinical field)✔ Strong clinical assessment and medical review expertise✔ Understanding of adverse event reporting and regulatory documentation✔ Excellent communication and analytical skills If you are a medical professional with an interest in regulatory functions and clinical safety, this position provides an excellent opportunity to apply your skills in a pharmaceutical setting. How to Apply Interested candidates can apply directly through clicking “Apply” on the MSN Laboratories job page and submitting an updated CV highlighting clinical experience and regulatory interests.

WhatsApp Group Join Now Instagram Group Join Now Are you a detail-oriented professional with experience in regulatory documentation and compliance? Medtronic is hiring a Regulatory Affairs Specialist in Hyderabad, Telangana — an excellent opportunity to work with a global leader in medical devices and healthcare technology. About the Company Medtronic is one of the world’s leading medical technology innovators, dedicated to improving healthcare outcomes across the globe. Known for its cutting-edge devices and life-changing solutions, Medtronic’s mission is to alleviate pain, restore health, and extend life. Job Overview: Regulatory Affairs Specialist Location: Hyderabad, Telangana, IndiaCompany: MedtronicJob Type: Full-timeExperience Level: 4 to 8 years (approx.)Education: B.Tech or relevant degree required As a Regulatory Affairs Specialist, you’ll play a crucial role in ensuring that Medtronic’s innovative healthcare products comply with regulatory standards in India. You’ll coordinate documentation, submissions, and compliance processes that directly impact product approvals and patient safety. Key Responsibilities At Medtronic, your day-to-day may include: Required Skills & Qualifications To succeed in this role, Medtronic prefers candidates with: ✅ Education: B.Tech (Mandatory)✅ Experience: 4+ years in regulatory affairs or related compliance role✅ Strong documentation and analytical skills✅ Ability to manage cross-functional regulatory tasks✅ Understanding of medical device compliance and regulatory frameworks This role is ideal for professionals who enjoy maintaining high regulatory standards and making a real difference in product safety and quality. Why Work at Medtronic Working at Medtronic means: ✨ Being part of a mission-driven global team✨ Exposure to cutting-edge medical technologies✨ Competitive benefits and professional growth opportunities✨ A supportive work culture that values innovation and inclusion How to Apply You can apply for this position directly through CLICK HERE nsure your CV highlights your regulatory experience and relevant compliance expertise.