Latest BSc/MSc Pharma Job – at Amneal in Ahmedabad
Amneal Pharmaceuticals is actively hiring for the position of Senior Executive – Manufacturing in Ahmedabad, Gujarat. This role involves critical responsibilities in sterile production environments, including document control (BMRs, BPRs, SOPs), regulatory compliance, and quality assurance. Candidates with degrees in B.Sc., M.Sc., B.Pharm, or M.Pharm and experience in GMP-regulated pharma manufacturing are encouraged to apply for this career-advancing opportunity.
About Company
We are a leading pharmaceutical company located in Ahmedabad City, Gujarat, India. At Amneal Pharmaceuticals, we are dedicated to providing high-quality healthcare products to improve the lives of our customers.
Job Title: Senior Executive-Manufacturing
Location: Ahmedabad City, Gujarat, India
Job Description
Responsibilities for BSc/MSc Pharma Job:
- Responsible for document management like BMRs, BPRs, master SOPs etc.
- Responsible for preparation & review of the master documents of production.
- Responsible to ensure UAF working in area.
- Responsible for handling change control, deviations, investigation & CAPA, etc.
- Responsible to check all records and logbooks related to manufacturing, sterilization, washing and sterilization of equipment’s.
- Responsible for preparation, review, revision, control, and implementation of standard operating procedures of the sterile manufacturing department.
- Responsible to ensure cleaning and sanitization of General & Controlled area.
- Inform immediately to department functional head for any observation/disturbance with respect to documents and machines found in the area.
- Responsible for monitoring all activities related to General & Control area.
Additional Activities: Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance. Responsible for line clearance activity before commencing the operations.
Skills:
- Complying with Good Manufacturing Practices (GMP) and regulatory standards (USFDA, MHRA, WHO, etc.).
- Completing Batch Packing Records (BPRs), logbooks, and deviation reports.
- Maintaining traceability and following SOPs strictly.
Qualifications
Educational Background: B.Sc. / M.Sc. / B. Pharm / M.Pharm
Keywords: BMRs, BPRs, SOPs, sterile manufacturing, Job, GMP, USFDA, MHRA, WHO, Batch Packing Records
