Amneal Pharma - Multiple Openings (43 Openings) for M.Pharm / B.Pharm / D.Pharm / B.Sc / ITI / Diploma Candidates - PHARMA WISDOM

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Sunday, 15 November 2020

Amneal Pharma - Multiple Openings (43 Openings) for M.Pharm / B.Pharm / D.Pharm / B.Sc / ITI / Diploma Candidates


Opening for Injectable Ophthalmic line, Aseptic area - A' bad SEZ

We are looking for competent, dynamic and motivated candidates for suitable positions for Injectable unit for our Ahmedabad SEZ Matoda Plant.


Ophthalmic Line:
Qualification: M.Pharm / B.Pharm / Diploma Engineering/ D.Pharm / B.Sc / ITI
Total Experience: 02 to 07 years
Area: Ophthalmic Aseptic area

Position: Officer: 13

Operator: 30

Desired Profile:

  • To observe & follow all rules and regulations of the production department.
  • Material transfer through active passive valve system
  • Must be from Parenteral background
  • To be aware and responsible for achieving quality objective and fulfilling the requirements of the quality of the company's service by means of applicable quality procedures.
  • Nanomill Operation, Manufacturing and Filtration vessel operation, CIP and SIP processing, Sterile API dispensing
  • Sound technical knowledge of Aseptic area and controlled are related activities.
  • Technical exposure and expertise on ophthalmic filling machine.
  • Knowledge of Regulatory guidelines and exposure of USFDA audits.
  • Knowledge of Eye drop filling machine and related batch mfg. process.
  • Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing area of injectable.
  • Expertise in batch manufacturing and preparation related activities.
  • Knowledge of equipment validation and qualifications in injectable.

Required Machine Exposure:

Three piece sterile eye drop filling machine operation (groninger)

Candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP/ GLP Knowledge and understanding of regulatory requirement is essential.

Note: Candidate should have 02 to 07 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organization.

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