Eisai Pharmatechnology & Manufacturing Pvt. Ltd. is a 100% subsidiary of 7.5 Billion $ Eisai Co. Ltd., Japan. It plans to set up a state-of-the-art Manufacturing and research facility for APIs and formulations at Ramky Pharma City Limited (SEZ), at Visakhapatnam in Andhra Pradesh, India. This global site shall be an industrial complex built with a research laboratories and drug-manufacturing facilities, incorporating Indias advanced chemical synthesis technology.
Eisai Pharmaceuticals India Private Limited – WALK-IN INTERVIEW @ INDORE ON SEP’ 10 & 11, 2022
- Department: OSD Manufacturing / Packing / Quality Control
- Open Positions: Operator / Supervisor / Assistant / Associate
- Qualification: B.Sc, M.Sc, B.Pharm, Diploma
- Experience: 3-6 yrs
- Work Location: Visakhapatnam
Roles and Responsibilities: OSD Manufacturing / Packing
- To follow and implement the systems, procedures, and practices for manufacturing operations and execution of production plan.
- Execution of Production Plan, monitoring of shop floor activity, Instant shop-floor planning, Meeting all the delivery schedules as committed in the Business Plan.
- Reporting and investigation of the Deviation or any Non-compliance in the Production area.
- Compliance to cGMP and Global Regulatory requirements for Drug Product facility.
- Carry out in-process checks, on line documentation as per the respective SOP and Batch records
- Preparation of SOPs and various GMP documents.
Desired Candidate Profile
Having good experience and exposure in Dispensing, Granulation, Compression, Coating area (Preference to Enteric & Sugar Coating), and packing (Bottle, Blister, Bulk Packing).
- Graduate / Post Graduate in Pharmacy / Sciences with 03 to 04 years of experience in Manufacturing of Solid Dosage Form (Tablets and Capsules), have handled equipment in manufacturing / packing.
- Shall have good knowledge of Manufacturing / Packing equipment.
- Proven ability to work independently and in a team environment.
- Extensive experience in manpower handling, team building and resolving shop floor issues arising out of personnel inefficiencies or technical incompetence.
- Strong knowledge of regulatory guidelines for US FDA, MHRA, TGA, MCC, etc and Industry knowledge
