Postgraduate degree including the integrated PG degree in Biotechnology, Microbiology, immunology, biochemistry, human genetics.

Knowledge and experience in the international regulatory environment of clinical trial applications, non-clinical and/or clinical variations to marketing authorizations and product labelling relevant for biotechnology and/or oncology products

Having Injectable Experience of Shop floor activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions

Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidances and defined regulatory strategies.

Finecure Pharmaceuticals Limited is a leading manufacturer and marketer of Pharmaceutical formulations in several therapeutic segments.

M.Sc, M.Pharm, MS Pharm in Organic Chemistry, Medicinal Chemistry.

Diploma in Pharmacy from Govt, recognized institute. Registered under the Pharmacy Council. 

MSc in Biochemistry, Microbiology, Biotechnology OR M.Pharm in Pharmacology with NET, GATE, GPAT national level examination qualification.

Retired para-medical staff in the relevant level or higher, within 65 years of age and having prescribed medical fitness, are eligible to apply. The employees who have retired in the relevant categories in higher pay levels, upto 3 levels higher than the posts being filled up through re-engagement

The applicant should possess an M.D./M.S./Ph.D. degree (M.D./M.S./M.D.S. or MBBS/BDS/MVSc./M.Sc./M.Pharma/M.Tech or equivalent with Ph.D. in health/biomedical research) with at least fifteen years of experience

Ensure compliance with global and local procedural documents and local implementation of Patient Safety objectives, policies, processes and procedures. 

Are you passionate about quality and keen to build your career in the pharmaceutical industry? We are hiring enthusiastic and dedicated individuals for our Quality Control (QC) Department.

Preparation of batch manufacturing records, process validation protocol/report of DP area and its associated records

2-6 years of experience in operating of Granulation Glatt, Compression fette, Coating, Primary Packing CVC, Labelling bulk packing, Auto Cartonator

Exposure to OSD Manufacturing operations like Compression, Pellet coating, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will be added advantage.

 IPQA Mfg. & Packing, Shop floor activities, Review of equipment audit trails, BMR, BPR review, line clearance. Process Validation, equipment, Utility qualification.

1st class B.Sc or MSc in Life Sciences or Biotechnology. Three years of post qualification experience in nucleic acid deliversy via nanocarriers.

Novartis has announced the top-line results of its Phase III GCAptAIN study, evaluating Cosentyx (secukinumab) in patients with giant cell arteritis (GCA) a serious inflammatory condition that primarily affects adults over the age of 50.

Merck has announced that the U.S. Food and Drug Administration (FDA) has accepted and granted priority review for a supplemental Biologics License Application (sBLA) for Winrevair (sotatercept-csrk).