Assistant / Associate - Batch Manufacturing

Amneal Pharmaceuticals · Ahmedabad

  • Experience3–6 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Levelmid
  • Posted21 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 Assistant/Associate batch manufacturing role at Amneal Pharmaceuticals in pharmaceutical manufacturing, responsible for monitoring manufacturing area activities including batch manufacturing, CIP and SIP of vessel, and line clearance in aseptic production. You will fill logs and BMRs and follow SOPs and cGMP/Good Document Practice, including preventive maintenance, cleaning & sanitization, filter integrity, and UAF working. Required qualifications are ITI or Diploma in Mechanical Engineering with 3-6 years of experience, specifically in aseptic area manufacturing of injectable products; location is Ahmedabad, Gujarat, India.

Full job description

Key Responsibilities

JOB DESCRIPTION

Responsible to attend the training as per schedule and to ensure the training and work as per TNI.Responsible to perform and monitoring all the activities related to Manufacturing area.Responsible to fill the logs, BMRs and documents of area as per SOP and work execution. Responsible to follow the preventive maintenance schedule of machines, instruments and equipment’s of manufacturing area.Responsible to ensure the cleaning and sanitization of machines, instruments and equipment’s and manufacturing area.Responsible for line clearance activity before commencing the operations, CIP and SIP of VesselResponsible to operate the machines : Manufacturing Vessel and CIP moduleInform immediately to concern supervisor for any observation/disturbance found in the aseptic area.Responsible to update on self-hygiene, cleaning & sanitization of area, follow SOPs, filled the document, of area.Responsible to fill the log of area as per SOP and work execution.Responsible to ensure UAF working in area.To follow the cGMP, Good Document Practice and discipline in the department

Qualifications

Qualification Requirement: ITI/ Diploma in Mechanical Engineering

Exp.: 3-6 years

Skilled Operator required for CIP & SIP of Vessel, Filter integrity and Batch manufacturing activityCandidate must have experience in the aseptic area for Manufacturing of Injectable Products