B Pharm Job at Amneal Pharmaceuticals | Apply Now
If you’re looking for a B pharm job in the pharmaceutical manufacturing sector, this opportunity at Amneal Pharmaceuticals could be your next big career move. With a focus on quality management systems (QMS), compliance, and sterile manufacturing, this role offers hands-on experience in a regulated environment. Whether you are exploring m pharm job opportunities or planning to grow through amneal careers, this position provides the perfect platform to enhance your expertise.
- Job Position: Executive Manufacturing QMS and Compliance (Injectable)
- Location: Ahmedabad City, Gujarat, India
- Job ID: 5795
About the Company
B pharm job seekers exploring amneal careers will find Amneal Pharmaceuticals a globally recognized pharmaceutical company known for developing, manufacturing, and distributing high-quality generic and specialty medicines. The company focuses on innovation, regulatory compliance, and continuous improvement in pharmaceutical manufacturing.
Job Description
- B pharm job role involves responsibility for preparation & review of the master documents of sterile manufacturing for parenteral facility.
- Responsible for preparation and review of protocols and reports based on the requirements.
- Responsible for document management and preparation like BMR’s, BPR’s, master SOP’s etc.
- Responsible for the handling of change control, deviations, CAPA, investigation etc.
- Responsible to give training to all the subordinates, technicians and operators of the department.
- Responsible for Audit and compliance on manufacturing shopfloor.
- Knowledge of kaizen and continuous improvements.
-
Qualifications
- B.Pharm/M.Pharm candidates with minimum 3–5 years experience in manufacturing QMS/Process review/Compliance.
- This role is ideal for candidates searching for M pharm job roles or growth within amneal careers.
Key Responsibilities
- B pharm job includes preparation & review of master documents for sterile manufacturing.
- Handling documentation such as BMR’s, BPR’s, and SOPs efficiently.
- Managing change control, deviations, CAPA, and investigations.
- Ensuring compliance and audit readiness on the manufacturing shop floor.
- Training technicians, operators, and subordinates.
- Implementing kaizen and continuous improvement practices.
