Amneal Pharmaceuticals Job Vacancy For B.Pharm/ M.Pharm/ BSc/ MSc/ ITI/ Diploma

Amneal Pharmaceuticals Job Vacancy For B.Pharm/ M.Pharm/ BSc/ MSc/ ITI/ Diploma 

Amneal Pharmaceuticals Job Vacancy For B.Pharm/ M.Pharm/ BSc/ MSc/ ITI/ Diploma 

Opening For Sterile Manufacturing @Amneal (SEZ- Matoda)

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

INJECTABLE REQUIREMENT

1. Sterile Manufacturing (Injectable/Parenteral Unit)

Designation: Operator/Officer/ Sr. Officer /Executive/ Sr. Executive

Qualification: ITI/ B.Sc/ Diploma / B. Pharm / M.Sc/ M. Pharm

Total Experience: 02 to 07 years

Area: Aseptic & Controlled area operation (Filling, Sealing, filtration, intervention, Production QMS, Autoclave, Batch Manufacturing, terminal sterilization etc.)

Line: Ophthalmic, PFS, Lyo and Vial

Machine Exposure: Three piece sterile eye drop machine (Groninger), nenomil, isolator, Trucking, Bosch, fedegree & Optima

Open Position: 10 Officer & 30 Officer

 Desired Profile:

To observe & follow all rules and regulations of the production department.

Must be from Parenteral background & exposure to filling process is desirable.

To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures.

Sound technical knowledge of Aseptic area & Controlled area related activities.

Technical exposure and expertise on filling & Autoclave machine.

Knowledge of Regulatory guidelines and exposure of USFDA audits.

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.

Preparation & review of BMR-BPR

Preferred Exposure for Ophthalmic line: Three piece sterile eye drop filling machine operation (Groninger), Nanomill Operation, autoclave (Fedegari) Manufacturing and Filtration vessel operation, CIP and SIP processing

Knowledge of packing area operation and visual inspection

 

Candidate with good communication & interpersonal skills, computer knowledge, exposure to cGMP/ GLP and understanding of regulatory requirement will be preferred.

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

You can share CV on neha.modi@amnealindia.com