Micro Labs

Responsible for writing technical documents, including method development reports, validation protocols, and regulatory submissions.

Hands-on experience in facing regulatory inspections. Strong knowledge of Good Manufacturing Practices

Handling of batch manufacturing and filling activity with regulatory exposure in Sterile area.

Process Validation / BPR / BMR/ Equipment Qualification / Audit & Compliance / Engineering & Compliance / Investigation Team

Recruiting for our OSD Manufacturing Facility at Goa Plant

Candidates with hands on experience with Stability, finished products analysis of formulation products will be given preference. Handling of batch manufacturing and filling activity with regulatory exposure 3 Piece, BFS eye drops and Injectable in Sterile area. 

Expertise in establishing orthogonal approach in understanding the impurities in peptide APIs. Impurity Profiling for Peptides APIs comparing LC and HRMS, High molecular weight impurities and charge based peptide impurities.

Having good experience of method development on HPLC and GC instruments and other analytical instruments. Having knowledge of wet analysis

Candidates with experience in handling of sophisticated instruments e.g. HPLC, GC, UV, IR, Dissolution apparatuses and other laboratory equipment are preferred.