Quality Control Analyst will play a critical role in ensuring the integrity and safety of our pharmaceutical products. Youll conduct analytical testing on raw materials, in-process samples, and finished goods, adhering to Standard Operating Procedures and current Good Manufacturing Practices
To review protocols of method validation / verification, stability protocol, calibration, qualification document. To review raw material and packaging material specification / MOA.
Regulatory Affairs Executive is responsible contribute regulatory expertise in various aspects including regulatory submissions, right first-time dossiers, timely addressal of queries, etc. for various product categories such as Cosmetics, Commodities etc.
B.Pharmacy degree and Master degree from a recognized Indian or Foreign University. Experience in stereotaxic surgery, In-vitro and molecular biology techniques including RT-PCR, Western blot, In-situ hybridization etc. will be preferred.
The candidate must have First class graduate degree Science/ Pharmacy plus Three-year experience in relevant subject/field OR Post graduate in Science/ Pharmacy
Ph.D./MD/MS/MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc/M. Pharm/ME/M. Tech with at least one research paper in Science Citation Indexed journal.
Candidates with a master degree in Chemistry, Chemical Sciences, Pharmaceutical Chemistry with excellent academic record. CDRI-Research Internship Program supported by Cipla Foundation
M.Sc. in Biotechnology/ Biochemistry/ Microbiology/ Zoology from a recognized University or equivalent. Knowledge of the basic molecular and microbiology techniques
Candidates having a doctorate degree in Life Sciences or equivalent with a good publication record and fulfilling the norm/guidelines of DST Office Memorandum number DST/PCPM/Z-06/2022 dated June 26, 2023 are eligible to apply.