4-5

Knowledge of Production Planning, Co-ordination with Corporate Planning Team for smooth function, Scheduling of Manufacturing, Follow-ups with Inter-Departments for production activity.

M.Sc / B.Pharm / M.Pharm; Finished, AMV and Stability Section, knowledge of Instrument - HPLC, GC. Preferably know-how of Chromeleon Software

Infusion bags processing activities, In-process checks and Line Clearance activities, Handling of shift activities and manpower. Preparation of QRM, Incident and Investigation, OOL and OOS investigation, CC and CAPA, Protocols and CAPA closure reports.

Experience in Yeast Biology not limited to culture methods, strain modification, transformation and expression studies. Experience in Molecular Biology and Biochemical techniques, preferably in Saccharomyces Biology.

Good exposure require in IPQA - OSD and Sterile, Qualification OSD and Sterile. Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

Responsible for guiding and coaching employees, monitoring their productivity, and overseeing regular equipment safety and maintenance. Responsible for performing batch execution in Sterile Injectable lines manufacturing and packaging.

B.Pharm, M.Sc, M. Pharm with 3-8 years of experience in IPQA and manufacturing, packing QMS related activities in oral solid dosage form tablets, capsules, soft gelatin capsules, pellet Dosage form manufacturing facilities.

As a Senior Specialist, Expert Medical writer , you will support the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional/local levels. Independently prepares of clinical and regulatory documents such as Protocols, Clinical Study Reports, or Investigator Brochures.

Granulation, Compression, Coating, Liquid & Nasal, Machine Operators and Executives. Exposure in exhibit batch manufacturing, Product site transfers.