5+

Ensure that Bulk Viral Antigen production adheres to GMP standards on the shop floor, including line clearance, dispensing, and preparation processes. Examining and approving batch records, standard operating procedures, project plans, customer verification, and APS documents.

Handling equipment like HPLC, UPLC, GC dissolution tester, UV, Vis spectrophotometer, IR, KF titrator etc Trouble shoot in existing methods and support regular and stability analysis, Excipient analysis for formulation development

B.Pharm / M.Pharm; Compile, review and timely submission of Deficiencies responses as received from Health Canada. Support Cross-functional team like Analytical Development, Formulation Development during product development and align documentation as per HC guidelines.

Tevas Global Regulatory Affairs Policy and Intelligence team is at the forefront of regulatory policy and intelligence, transforming complex regulatory landscape updates into actionable insights to inform regulatory strategy and cross-functional strategic decision-making.

Handling of Analytical Instruments Like HPLC, LCMS, GC, Prep HPLC, SFC, Prep SFC, KF and SOR along with software. Method development by HPLC, GC for RM, Intermediate and final product.

Ensure ALCOA compliance, SLA adherence. Handle HPLC, UPLC, LCMS, GC, GCMS, Dissolution. Oversee method transfers & regulatory compliance.

Emcure is fast-growing Indian pharmaceutical company engaged in developing, manufacturing, and marketing a broad range of pharmaceutical products globally.

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma. Candidate must have hands on experience in Sterile, Parenteral, Aseptic, Filling, Sealing, Filtration, Production QMS, Batch Manufacturing.

Bachelors degree in Pharmacy, Science, or related field MBA preferred. Build and maintain strong relationships with cardiac surgeons, KOLs, and hospital administrators. Consistently achieve sales targets and identify opportunities to expand market presence.