Health Sciences, Health Care Professional degree required e.g., BSc, MS, PhD, RN, BSN, MSN, NP, RPh, B.Pharm, Pharm D Advanced degree preferred. Minimum 7-12yrs of Pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities
Applicants should have Masters with 0-3 years confirmed experience or a fresh PhD submitted within last one year in a life sciences field with a strong focus on protein design, protein purification, molecular biology, immunology, biotechnology or biochemistry.
In this role you are required to solve routine problems, largely through precedent and referral to general guidelines. Your primary interaction is within your own team and your direct supervisor
M.Pharmacy, preferably a PhD in Pharmaceutical sciences Join team for ground breaking discoveries in Drug Metabolism & Pharmacokinetics; Opportunities for talented individuals to join us as senior research associate/research scientist- In Vivo, senior research associate/principal scientist- In Vitro ADME and research associate/group leader- bioanalysis.
Proven track record of documentation review for accuracy and compliance to procedures essentially in analytical methods development, validation, transfer, stability studies, Design & Development.
Good knowledge in monitoring compliance by GSK and Third Parties with PVASC by carrying out routine reconciliations and compliance checks and communicating standard information to Third Parties as required with appropriate guidance.
M.Sc. / M Pharm / PhD. Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.