Company Jobs

Pharma knowledge of Solid orals & Quality process. USFDA, MHRA, ANVISA & Other regulatory exposure is preferred including ICH guidelines.

Analytical Method development. Handling HPLC, GC, UV IR, KF, Dissolutions

FFS, LVP, Flow wrapping, SHWSS, Terminal Sterilizer, Dry powder injection, Injection Labelling, Capsule Filling, Compression, Granulation, Coating

Experience in metabolite identification studies including proposing potential metabolite structure and determination of tentative structures of metabolites and their product ions from the LC-MS/MS data

Post Graduate, Graduate, Diploma in Pharmacy, Commerce, Science

Lead the assessment of existing ecosystems across key pillars, including client portfolio plans & objectives, technical architecture, data models etc. Collaborate with cross-functional teams to design and implement the optimal solution, ensuring seamless integration with existing processes

Candidates having Regulatory Exposure to USFDA, MHRA shall be preferred.

Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk.

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