Amneal Pharmaceuticals Pvt Ltd Walk In Interview for ITI/ BSc/ Diploma/ B Pharm/ MSc/ M Pharm
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| Amneal Pharmaceuticals Pvt Ltd Walk In Interview for ITI/ BSc/ Diploma/ B Pharm/ MSc/ M Pharm |
Walk-IN Drive on 17thDec'23 (Sunday) @ Amneal Pharma
We are looking for competent, dynamic and motivated candidates for suitable positions for Injectable/ parenteral units for our plants.
Walk In Interview Details:
Date : 17th December, 2023 (Sunday)
Time : 9:00 am to 2:00 Pn
Venue : Amneal Pharmaceuticals Pvt. Ltd. Plot No 15,16,17 Pharmez, Sarkhej Bavla Highway, Vil. Matoda, Ahmedabad 382213
Job Locations :
1) SEZ Matoda, Ahmedabad,
2) Palli Sachana,
3) Pipan Sanand
REQUIREMENT FOR INJECTABLE MANUFACTURING/ PRODUCTION DEPARTMENT:
Designation: Operator/ Officer/ Sr. Officer /Executive/ Sr. Executive
Department: Production (Sterile Manufacturing)
Qualification: ITI/ BSc/ Diploma / B Pharm / MSc / M Pharm
Total Experience: 02 to 08 years (Pharma experience only)
Area: Aseptic & Controlled area operation (Filling, Sealing, filtration, Autoclave, Batch Manufacturing, terminal sterilization, Visual Inspection testing/ VIT etc.)
Line: Ophthalmic, PFS, Cartridges, Lyophilizer and Vial
Machine Exposure: Filling machine (Groninger / Optima), Dyno Truking filling and sealing machine, Bosch filling machine, Steam sterilizer (Fedegree)
Desired Profile:
To observe & follow all rules and regulations of the production department.
Must be from parenteral background & exposure to Aseptic vial / Bottle filling process is desirable.
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 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
Manufacturing and Filtration vessel operation, CIP and SIP processing.
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 08 yrs. of relevant experience in USFDA regulatory approved pharmaceuticals.
Kindly carry your updated CV along with copies of CTC proof, Appointment letter, Increment letter, last 3 months salary slips, Bank statement, Education certificates & Marksheets, Aadhar & PAN card and passport size photograph, at the interview venue.
If you are unable to attend interview you can share CV on below email ids:
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