Manager, Regulatory Affairs
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique
Senior Executive-IP Litigation
Job Summary At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive commu
Senior Regulatory Affairs Specialist
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more tha
Assistant Research Scientist - Optometry
Department: SP CORE Location: Delhi, India Position: Optometrist Employment Type: Full-time Job Summary Pandorum Technologies Pvt. Ltd. is looking for an experienced Optometrist to support clinical an
Senior Regulatory Affairs Associate 5+ years experience in handling life cycle management of approved drug products (small molecules as well as biologicals including Vaccines, monoclonal antibodies) i
About the job Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vacci
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted a
Exe (Regulatory Affairs)
Job Title: Regulatory and Business Continuity Business Unit: R&D1 Regulatory Affairs Job Grade G12A Executive Location : Baroda At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by
Research Associate
Job Description Travel to site and monitor the clinical trial data generated at sites to make sure that ICH GCP guidelines, study protocol and applicable regulations are being followed. Take lead on s
We are looking for passionate and talented professionals to join our growing research team. 📍 Location: Bangalore 🔬 Requirements: M.Pharm (Pharmacology) 2–3 years of experience in Oncology / Immuno-On
Research Scientist - Microbiology
1. Responsible for performing microbiology lab qualification activity 2. Responsible for performing Sterility testing, bacterial endotoxin test, antibiotic microbial assay, microbial limit test and gr
Associate Research Scientist - DMPK
Conduct in vitro ADME studies such as solubility, stability, plasma protein binding, metabolism, drug-drug interactions, and Caco-2 permeability Instrumental in bioanalytical sample preparation, LC-MS
Research Scientist
Key Responsibilities Cell and Molecular Biology • Perform mammalian cell culture, primary cell culture, and cell-based functional assays. • Conduct nucleic acid delivery and transfection using lipid-
Research Scientist - Cellular Engineering
Job Profile: Support research activities involving primary and stem cell culture, cell-based functional assays, and molecular biology techniques. The role includes immunofluorescence imaging, producti
Research Scientist - Biomaterials
Job Requirements: · Conduct research on biomaterials targeted for tissue engineering and regenerative medicine applications and generate protocols for the same · Perform extensive physical,
Senior Research Scientist
Role : Senior Research Scientist - Biomaterials Job Requirements: · Conduct research on biomaterials targeted for tissue engineering and regenerative medicine applications and generate protocols for t
Sr. Research Scientist - Biomaterials
Conduct research on biomaterials and cellular engineering targeted for tissue engineering and regenerative medicine applications and generate protocols for the same Participate in interdisciplinary re
Clinical Research Medical Advisor
Summary Provide country-level clinical and medical leadership for Novartis clinical development programs by driving protocol feasibility, investigator engagement, recruitment strategy, an
Executive Manufacturing QMS and compliance Injectable
Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements
Executive Manufacturing QMS and compliance Injectable
Key Responsibilities: Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports bas