Walk-in Drive @ Amneal Pharma, SEZ- Matoda Plant for Production department (Injectable/ Parenteral) on 30thJun’2024 (Sunday)
We are looking for suitable candidates for INJECTABLE / PARENTERAL units for SEZ MATODA PLANT, AHMEDABAD
Interview Venue Details:
Date : 30thJun’2024 (Sunday)
Time : 9:00 am to 1:00 pm
Venue : Amneal Pharmaceuticals Pvt. Ltd.
Plot No 15,16,17 Pharmez, Sarkhej Bavla Highway,
Vil. Matoda, Ahmedabad 382213
JOB LOCATIONS: SEZ- MATODA, AHMEDABAD
1) REQUIREMENT FOR INJECTABLE MANUFACTURING/ PRODUCTION & PACKING DEPARTMENT
- Designation: Operator/ Officer/ Sr. Officer /Executive/ Sr. Executive
- Department: Production (Sterile Manufacturing)
- Qualification: ITI/ B. Sc/ Diploma / M. Sc / B. Pharm / M. Pharm
- Total Experience: 02 to 7 years (Pharma experience only)
Area: Aseptic & Controlled area operation (Filling, Sealing, filtration, Autoclave, Batch Manufacturing, terminal sterilization, Tunnel Operations, QMS Activities, packing, Visual Inspection testing/ VIT etc.)
Line: Ophthalmic, PFS, Cartridges, Lyophilizer and Vial, Bag Line, Robotic Line (Vial), Emulsion Line
Machine Exposure: Sterile eye drop 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.
- 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 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
- Filling machine operation (Groninger / Optima), Dynomill Operation, autoclave (Fedegari) Manufacturing and Filtration vessel operation, CIP and SIP processing
Candidate with good communication & interpersonal skills, computer knowledge, exposure to cGMP understanding of regulatory requirement will be preferred.
Note : Candidate should relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliant) organization.
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: [email protected] & [email protected]
