50+ OPENINGS AMNEAL PHARMA WALK IN INTERVIEW FOR PRODUCTION & QUALITY ASSURANCE DEPARTMENTS ON 5th JUNE 2022.

  AMNEAL PHARMACEUTICAL LIMITED WALK IN INTERVIEW FOR PRODUCTION & QUALITY ASSURANCE DEPARTMENTS ON 5th JUNE 2022. 

ABOUT AMNEAL PHARMACEUTICAL:

Amneal Pharmaceuticals Private Ltd is a high-quality producer of solid and Injectable generic products and one of the fastest-growing global generics producers. We believe that the world is our family and we are committed for consistently producing high quality affordable medicines. Amneal is expanding its operations in India and invites people who share its value of relentless pursuit of quality, integrity, treating each other with respect and encouraging the very best in everyone to join the Amneal family. To know more about us and what we stand for, please visit our website (www.amneal.com).

JOB DETAILS:

Amneal Pharmaceuticals Private Ltd looking for competent, dynamic and motivated ITI/ B.Sc/ Diploma / B. Pharm / M.Sc/ M. Pharm candidates for suitable positions for Operator/Officer/ Sr. Officer /Executive/ Sr. Executive in Manufacturing & Quality assurance Departments at Injectable unit for Ahmedabad SEZ Matoda Plant. Interested and eligible candidates can apply and attend walk in interview on 5th June 2022.

JOB DESCRIPTION:

1. Injectable Manufacturing 

DEPARTMENT: Sterile Manufacturing (Injectable/Parenteral Unit).

OPEN POSITIONS: 10 Officer & 30 Officer.

DESIGNATION: Operator/Officer/ Sr. Officer /Executive/ Sr. Executive

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

EXPERIENCE: 02 to 07 years

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

Line: Ophthalmic, PFS, Lyo and Vial

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

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.

2. Injectable Quality Assurance.

DEPARTMENT: Quality Assurance (Validation/IPQA/EM) – Injectable/Parenteral Unit).

VACANT POSITIONS: 11

DESIGNATION: Officer/Sr. Officer/ Executive/ Sr. Executive

QUALIFICATION: B.Pharm/M. Pharm/ M.sc Microbiologist

EXPERIENC: 02 to 07 years

AREA: IPQA, Line Clearance, BMR-BPR review, Aseptic area, Media fill, Environment monitoring, Plate settlement, Validation, qualification, Equipment qualification, Process validation, protocol preparation, etc.

DESIRED PROFILE:

1. Responsible for preparation, review and implementation of Standard Operating Procedures of Quality Assurance department.

2. Should have sound knowledge and experience in Environmental Monitoring (Air Sampling, Settle Plate, Surface Monitoring, Personnel Monitoring)

3. Responsible for the review of BMR/BPR.

4. Responsible for Document management like BMR, BPR, Master SOP, training record etc.

5. Responsible for reserve sample management, annual review and destruction as per procedure.

6. Responsible for tracking of stability sample collection as per protocol.

7. Responsible for stage wise line clearance activity before commencing the operations like dispensing, manufacturing, filling, Lyophilization, sealing, labelling and packing operations.

8. Supervision of sampling activity for in-process and finished samples for analysis and other samples requirement as per protocols (Process Validation, Cleaning Validation etc.)

9. Responsible to provide and fulfil the documents requirement of Regulatory Affairs department for filing or other requirements.

10. This includes documents review, protocol preparation, qualification executions and support to CFT and report compilation.

11. All the equipment qualification (URS, DQ, FAT) i.e. Filling line, Vessels, Packing machines, UAFs, DPBs, Mobile carts, documents review and approval etc.

12. All the utility qualification (URS, DQ, FAT, IQ, OQ, PQ) i.e. HVAC, Compressed air, Nitrogen gas, WFI (Phase I, Phase II, Phase III), PW (Phase I, Phase II, Phase III), Pure Steam, Smoke study, etc.

13. Media fills (All process i.e. Liquid, Suspension, Emulsion as applicable)

14. Process validation, cleaning validation, CEHT, DEHT

15. Facility qualification, FAT

16. Activities other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HOD’s instruction and guidance.

WALK-IN DETAILS:

DATE: 05-Jun-22 (Sunday)

TIME:  9:00 am to 3:00 pm

VENUE: for Interview: Amneal Pharmaceuticals Pvt. Ltd. Plot No 15,16,17 Pharmez, Sarkhej Bavla Highway, Vil. Matoda, Ahmedabad 382213.

HOW TO APPLY:

Interested candidates can share resume on.

neha.modi@amnealindia.com.

NOTE:

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.