Amneal 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.
Amneal Pharma Walk-in Interviews for Manufacturing (OSD& INJECTABLE) on 20th October, 2024 (Sunday). We are looking for competent, dynamic and motivated candidates for suitable positions in OSD & INJECTABLE Manufacturing, Ahmedabad.
Walk-In Interview Details:
- Date: 20th October 2024(Sunday)
- Time: 9:00 am to 2:00 pm
- Venue: Hampton By Hilton, 14, Friends Co-Operative Society, Alkapuri,
Vadodara, 390007.
(Oral Solid – OSD Requirement)
1. Manufacturing & Packing (Tablet/Capsule)
- Designation: Operators/ Officer/ Sr. Officer /Executive
- Qualification: B. Pharm, B.sc, Diploma, ITI, B.E
- Total Experience: 02 to 06 years
- Job Location : SEZ MATODA, Ahmedabad
- Area: Coating, Granulation, Compression, Packing (Bottle Packing only)
- Machine Exposure along with 21 CFR compliance: RMG, FBE, Fette compression, Auto coaters, bottle packing line with Track & Trace system.
Desired Profile:
- Candidates should have hands on experience along with knowledge of 21 CFR compliance in equipment’s like RMG, FBE, V-Blender, Fette compression machine, Autocoater, CVC Line and packaging line equipment with Track and Trace system.
- Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing/Packaging area of OSD.
- Able to understand & have relevant knowledge of SCADA operation & 21 CFR requirements.
- Able to understand & operate fluid Bed equipment
- To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches.
- To maintain the areas and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition.
- To impart training of operation and cleaning related SOP to all subordinates and operators
- Co-ordination for IQ / OQ for any new equipment / system
- To perform PQ for any new equipment / system
- To follow all concern departmental SOP’s for day to day operation and cleaning
- To handle and manage material movement as per defined procedure and approved Batch Manufacturing Record
- To perform online documentation with respect to departmental procedures as per good documentation
- Maintaining the change parts for all equipment at manufacturing.
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(Injectable Manufacturing Requirement)
2. Sterile Manufacturing
- Designation: Operators/ Officer/ Sr. Officer /Executive
- Qualification: B. Pharm, B.Sc, Diploma, ITI, B.E, M.Sc, M.Pharm
- Total Experience: 02 to 06 years
- Job Location: SEZ MATODA I PALLI I PIPAN Ahmedabad
- Area: Aseptic & Controlled area operation (Filling, Sealing, filtration, Autoclave, Batch Manufacturing, terminal sterilization, Tunnel Operations, QMS Activities, packing etc.)
- Line: PFS, Lyophilizer and Vial, Bag Line, Emulsion Line
- Machine Exposure: filling machine (Groninger / Optima), Dyno Truking filling and sealing machine, Bosch filling machine, Steam sterilizer (Fedegree)
Desired Profile:
- Expertise in batch manufacturing and preparation related activities.
- 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.
- Technical exposure and expertise on filling & Autoclave machine.
- Knowledge of change control, Deviation, CAPA, and documentation in manufacturing area of injectable.
- Knowledge of equipment validation and qualifications in injectable.
- Preparation & review of BMR-BPR
- Exposure of regulatory audits like USFDA/ TGA/ EU etc.
Candidate with good communication & interpersonal skills, computer knowledge, exposure to cGMP/ ALCOA, ALCOA++ & understanding of regulatory requirement will be preferred.
Note : Candidate should have 02 to 06years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) 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.
Interested candidates who are unable to attend interview, can share their cv on email-id indiacareers@amneal.com
Thanks & Regards
Chandani Daswani
Sr. Manager – HR
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