M.Sc. in any discipline of Life Sciences with first class marks. GATE / CSIR / UGC-NET is compulsory. Good knowledge of synthesis and functionalization of nanoparticle.
You will be responsible for preparation, review, and approval of Cleaning Master Validation Plan, Cleaning Validation and Verification Protocols and Reports, Acceptance Criteria documents, Cleaning Validation matrix, and Periodic Monitoring Schedule
Master or PhD of pharmaceutical. Perform statistical analyses of data from the laboratories using R and possibly other languages SAS or standard statistical software used in Sanofi, JMP, SIMCA, internal tools. Sanofi
M.Sc. in Chemistry / M. Pharm in Pharmaceutical Analysis. Strong communication, interpersonal, and presentation skills. Proven experience in team handling and leadership.
Postgraduate in the field of Life Sciences or Pharmaceutical Sciences or any other allied Life sciences. Exploiting synthetic lethality of type II NADH dehydrogenases for complete sterilization of Mycobacterium tuberculosis
M.Sc. (Life Sciences: Biochemistry, Biotechnology, or any branch of Life Sciences) degree holders. OR MBBS/BDS/MS Pharm/M. Pharma/ME/M. Tech degree holders.
Zenotech Labs invites QA and QC professionals to manage IPQA activities for injectables, oversee packaging operations, and ensure BMR/BPR review with cGMP/GDP compliance.
Manager Scientific Writing involves updating / creating and reviewing scientifically / medically accurate content for commercial and medico-marketing assets. Novartis. Advanced degree in life sciences, pharmacy, medicine or related field.
Masters Degree in Pharmaceutics or Pharmaceutical Sciences (First-class) from a recognized university. The candidate will be eligible to apply for the Ph.D. position next semester.