Executive Manufacturing QMS and compliance Injectable

Amneal Pharmaceuticals · Ahmedabad

  • Experience3–5 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Levelmid
  • Posted17 Sept 2026

About Amneal Pharmaceuticals

Amneal Pharmaceuticals is hiring in Ahmedabad in pharma biotech. This role looks for around 3+ years of experience.

The role

A mid-level executive manufacturing QMS and compliance role at pharmaceutical manufacturing company Amneal Pharmaceuticals, responsible for preparing and reviewing master documents for sterile parenteral manufacturing, managing BMRs/BPRs and master SOPs, and handling change control, deviations, CAPA, and investigations for audit and shopfloor compliance. Requires kaizen and continuous improvement knowledge, plus B.Pharm/M.Pharm with 3-5 years of experience in manufacturing QMS, process review, and compliance. Location is Ahmedabad, Gujarat, India, working onsite.

Full job description

Job Description

Responsible 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

Qualification: B.Pharm/M.Pharm candidate with minimum 3-5 years experience in manufacturing QMS/Process review/Compliance.