Wednesday, June 17, 2020

Multiple Openings at Amneal Pharmaceuticals for Injectable Unit

Opening for Injectable Ophthalmic, Vial, PFS and Lyo line - 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 & Controlled area
Position: Officer: 20
Operator: 50
Vial, PFS and Lyo Line:
Qualification: M. Pharm/ B.Pharm/ Diploma Engineering/ D. Pharm/ B.Sc/ ITI
Total Experience: 02 to 07 years

Area: Ophthalmic Aseptic & Controlled area
Position: Officer: 10
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), Autoclave operation (Fedegari)
Required Candidate profile:
The 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) organisation.
Those who have already attended interview in last 6 month need not appear again for interview

No comments:

Post a Comment