The Drugs Technical Advisory Board, DTAB, has recommended changes to the regulatory requirements for manufacturing drugs intended for clinical trials, bioavailability and bioequivalence studies, analytical testing and non-clinical studies.

M.Sc. in Chemistry / Chemical Sciences/Pharmaceutical Chemistry/Pharmaceutical Sciences and qualified CSIR-UGC/ICAR/ICMR NET incl. lectureship / assistant professorship or GATE. CDRI October Interview 2026

B.Sc. Life Science / B.Pharm with Post Graduate Diploma in Clinical Research Or M.Sc. in Life Science/ M. Pharm with PG Diploma in Clinical Research. TATA MEMORIAL CENTRE

Pfizer, we recognize that our colleagues are our most valuable resource in advancing biomedical innovation and improving patient health outcomes. Our collective ambition is to change a billion lives per year, and we achieve this by making patients the focus…

Basic knowledge on TEVA product portfolio, their therapeutic areas expertise, mechanism of actions and its product/patient safety index.

Supervision of dispensing, compounding and filtration activities; cGMP, SOP and BMR compliance; line clearance and in-process checks; batch documentation and reconciliation; coordination with IPQA, QC, Microbiology and Engineering; handling of deviations…

The applicants should hold a M.Sc. degree in Life Science, Chemistry, Biotechnology, Biochemistry, Molecular Biology, Bio-medical engineering, Nanoscience & Nanotechnology and other related areas/B.S. 4 years programme /BPharm/Integrated BS-MS/BE/BTech or…

Adaptis was established in August 2020, with its corporate office in Panaji, Goa, and branch office in Pune, Maharashtra, India.Post : MICC-EXECUTIVEICSR-EXECUTIVE PharmacovigilanceExperience : 1-3 yearsQualification : M.Pharm / Pharm.DLocation : Pune

Conduct laboratory trials and formulation/process evaluation. Support aseptic processing and sterile manufacturing development. Evaluate formulation parameters and excipient compatibility.

Diploma in Pharmacy (D. Pharm), Bachelor of Pharmacy (B. Pharm), or Doctor of Pharmacy (Pharm. D) from a recognized institution, registered with a TS State Pharmacy Council.

Ph.D / MD/MS / MDS or equivalent degree or having 3 years of research teaching and design and development experience after M/Sc/M.Pharm/ME/M.Tech with at least one research paper in Science Citation (SCI) Journal.

The applicant should hold a PhD degree in Science or Engineering or MD/MS/MDS degree. The applicant should have at least four years of service remaining before superannuation as of the date of submission of the proposal.

PhD in Pharmacy / Pharmacology / Public Health /Statistics / Epidemiology/Health Sciences) or equivalent degree or equivalent post- graduate degree or having 3 years of research, teaching and design and development experience after MVSc/M.Pharm/ME/M.Tech…

Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries

B.Pharm / D.Pharm (Council Registration), Candidates who are 18 years and above and below 44 years of age are eligible to apply for the above-mentioned posts.

B.S. 4 years programme / BPharm / MBBS / Integrated BS- MS / MSc / BE / BTech or equivalent degree, with 55% marks and passing of NET / GATE test in any branches of Life Sciences

MSc in Biological Sciences / MPharm from a recognized University/Institution or equivalent, and research experience in cell culture, molecular biology techniques, animal handling, clinical sample analysis and related work. CSIR-Indian Institute of Integrative…

PhD. in Chemical / Biological/ Pharmaceutical Sciences in relevant fields from a UGC/AICTE recognized University / Institute. National Dope Testing Laboratory

looking for a meticulous professional to lead drug product manufacturing and sterile formulation operations, ensuring adherence to Current Good Manufacturing Practice, cGMP and safety norms.