Pharma Jobs

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.

WhatsApp Group Join Now Instagram Group Join Now Are you a life sciences professional looking for clinical scientist opportunities in India? Syneos Health, a globally recognized biopharmaceutical solutions company, has announced a job vacancy for the position of FSP Clinical Scientist at its Serilingampalli, Telangana location. This role is ideal for candidates with a strong background in clinical data review, scientific analysis, and clinical research methodologies. About Syneos Health Syneos Health is a leading fully integrated biopharmaceutical solutions organization that partners with pharmaceutical and biotech companies worldwide to accelerate clinical development and commercial outcomes. With a focus on science, innovation, and patient-centric solutions, Syneos Health offers exciting career opportunities for professionals who want to make an impact in the healthcare and life sciences industry. Job Summary – FSP Clinical Scientist This Syneos Health job vacancy in Telangana is ideal for professionals who enjoy scientific data review and contributing to high-quality clinical development processes. Key Responsibilities As an FSP Clinical Scientist, your primary duties will include: This role blends scientific rigor and clinical analysis, making it a strong fit for candidates passionate about contributing to innovative therapies. Required Skills & Qualifications To excel in this Syneos Health job vacancy, candidates should ideally have: This position is perfect for professionals with a passion for clinical science and a desire to grow within the pharmaceutical research sector. Job Location Serilingampalli, Telangana, India – a key hub for clinical research and life sciences activities in the country. Why Join Syneos Health? Working at Syneos Health offers: If you’re seeking a clinical science role that blends rigor and impact, this is a strong opportunity to advance your career. How to Apply

WhatsApp Group Join Now Instagram Group Join Now US Pharmacopeia is a global nonprofit organization that sets public standards for medicines, food ingredients, dietary supplements, and healthcare products. USP plays a critical role in advancing quality and safety within the pharmaceutical industry by developing and maintaining trusted standards used worldwide. Position Summary – Scientist III (CDL) This US Pharmacopeia job vacancy in Hyderabad offers a pivotal role for analytical scientists involved in method development and validation, supporting global quality standards for medicines. Key Responsibilities As Scientist III – CDL, you will: Required Qualifications & Experience To qualify for this US Pharmacopeia job vacancy, candidates should have: Why Join US Pharmacopeia? This role offers: ✅ A chance to work on globally recognized compendial standards✅ Exposure to cutting-edge analytical research in pharmaceuticals✅ Opportunity to influence quality and regulatory outcomes✅ Collaborative and inclusive work environment focused on scientific excellence Skills That Make Candidates Stand Out 💡 Deep analytical method expertise💡 Experience interpreting regulatory compendial requirements💡 Ability to operate complex instruments with precision💡 Strong writing and reporting skills💡 Critical thinking and problem-solving abilities How to Apply APPLY HERE 👉 Don’t forget to include keywords such as analytical method development, HPLC, GLP, and pharmaceutical standards to strengthen your application.

WhatsApp Group Join Now Instagram Group Join Now If you are searching for a pharma supply chain job in Hyderabad, here’s a great opportunity to join one of India’s fast-growing pharmaceutical companies. MSN Laboratories has opened a job vacancy for the position of Executive / Sr Executive – Analytical Capital SCM Formulations in the Supply Chain Management department. This role is ideal for procurement and supply chain professionals with a good understanding of SAP and material sourcing. Candidates seeking a career in the pharma manufacturing industry can take advantage of this opening to grow professionally. About MSN Laboratories MSN Laboratories is known as one of India’s fastest expanding pharmaceutical companies with an emphasis on innovation, quality, and growth. The organization has deep expertise in manufacturing formulations and APIs and offers exciting roles for energetic professionals across supply chain and operations. Job Summary – Executive / Sr Executive – SCM 📍 Role: Executive / Sr Executive – Analytical Capital SCM Formulations📍 Company: MSN Laboratories📍 Location: Hyderabad, Telangana, India🕐 Job Type: Full Time📅 Posted: Recently on LinkedIn💼 Job Function: Supply Chain / Procurement / Materials Management Key Responsibilities As an Executive / Sr Executive – Analytical Capital SCM, your responsibilities will include: Required Skills & Qualifications To apply for this MSN Laboratories job vacancy, candidates should have: Why Join MSN Laboratories? APPLY HERE

WhatsApp Group Join Now Instagram Group Join Now Indoco Remedies Limited, a leading pharmaceutical company with a strong global presence and regulatory approvals like USFDA and UKMHRA, has announced a walk-in interview for its Sterile Formulations Manufacturing Facility in Goa. This Indoco Remedies Limited walk in interview is open for experienced candidates having hands-on exposure in injectable and ophthalmic products. Multiple openings are available across production, quality, microbiology, and engineering departments. About Indoco Remedies Limited Indoco Remedies Limited is a reputed pharmaceutical organization with more than 75 years of excellence. The company operates globally and follows international regulatory standards, offering stable careers and professional growth in the pharma sector. Job Openings at Indoco Remedies Limited Production Department Officer / Executive / Assistant Manager (Shift In-Charge) Associate (Operator) Quality Assurance (QA) Officer / Executive / Assistant Manager Quality Control (QC) Officer / Executive Microbiology Officer / Executive / Assistant Manager Engineering Officer / Executive / Assistant Manager Indoco Remedies Limited Walk in Interview Goa 2026 Schedule Dates: Time: 9:30 AM to 4:00 PM Interview Venue Indoco Remedies Limited – Plant IIL-32, 33, 34, Verna Industrial Estate,Verna, Goa – 403 722 (India) Documents Required Important Notes Contact Details Email:hrd2@indoco.comcareer@indoco.com Contact Numbers:08326624209 / 7391054322

WhatsApp Group Join Now Instagram Group Join Now If you are looking for a pharma job opportunity in 2026, this is a great chance to build your career with a reputed pharmaceutical company. Pellets Pharma Limited has officially announced multiple openings across quality, research, regulatory, and support departments for experienced as well as fresh candidates. This Pellets Pharma Limited job vacancy is suitable for candidates holding MSc, M.Pharmacy, BSc, MBA, and HR qualifications who are seeking stable growth in the pharmaceutical industry. About Pellets Pharma Limited Pellets Pharma Limited is a well-established pharmaceutical company known for its quality-driven manufacturing, research excellence, and compliance with regulatory standards. The company offers a professional work environment, career growth opportunities, and exposure to advanced pharma operations. 📌 Current Job Openings at Pellets Pharma Limited 🔬 Quality Control (QC) 💊 Formulation Research & Development (FR&D) Analytical Research & Development (AR&D) Regulatory Affairs (RA) IPQA (In-Process Quality Assurance) Warehouse Department Human Resources (HR) Job Location Plot No. 8 & 9, TSILC – EPIP,Pashamylaram, Patancheru,Sangareddy, Telangana – 502307 Important Note Only male candidates are preferable for the above positions. How to Apply for Pellets Pharma Limited Job Vacancy Interested and eligible candidates can apply through the following methods: 📧 Email: recruitment@pelletspharma.com📱 WhatsApp / Contact Numbers: 👉 Send your updated CV with the relevant job title mentioned.