Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX), headquartered in Bridgewater, NJ, is a global pharmaceuticals company. We make healthy possible through the development, manufacturing, and distribution of a diverse portfolio of over 280 generic and specialty pharmaceuticals, primarily within the United States. In its Generics segment, the Company is expanding across a broad range of complex product categories and therapeutic areas, including injectables and biosimilars.
- Vacancy details:
- Department: QA (Environmental Monitoring, IPQA & Validation) (Injectable/ Parenteral)
- Experience: 2 to 7 Years
- Qualification: B.Sc. (Micro) / M. Sc (Micro) / B. Tech. (Biotech.) / M. Tech (Biotech)/B. Pharm / M. Pharm
- Salary: NA
Job Description: Greeting from Amneal pharmaceuticals !!!
Important Details :
-
Work Location: Ahmedabad
- Post of date: 21/11/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Amneal Pharma Walk-in Drive for QA (Environmental Monitoring, IPQA & Validation) (Injectable/ Parenteral) on 23rdNov’24 (Saturday)
We are looking for competent, dynamic and motivated candidates for suitable positions for Injectable/parenteral units for Pipan, Sanand Plant, Ahmedabad.
Date : 23rd November 24 (Saturday)
Time: – 9:00 AM to 1:00 PM
Venue : Amneal Pharmaceuticals Pvt. Ltd.
Plot No: 161/1, Sanand Bavla Highway Road,
Village : Pipan, Sanand, Ahmedabad, Gujarat 382110
Job Location : Pipan, Sanand, Ahmedabad,
INJECTABLE REQUIREMENT
Quality Assurance Department (Injectable/Parenteral Unit)
1. Quality Assurance – Environmental Monitoring (Microbiologist)
- Designation : Trainee/ Officer/ Sr. Officer / Executive
- Department : EM (Environmental Monitoring)
- Qualification : B.Sc. (Micro) / M. Sc (Micro) / B. Tech. (Biotech.) / M. Tech (Biotech)/
- Total Experience: 1 to 05 years in injectable/ sterile manufacturing plant.
- Shift Type : Rotational Shift timing
- Job Location : Pipan, Sanand, Ahmedabad
Job Description:
- Environmental monitoring of manufacturing clean room area.
- Non-viable particle monitoring of manufacturing clean room area.
- Compressed air /nitrogen gas monitoring and Personnel monitoring.
- To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g. plates, swabs, etc.
- To perform line clearance activity.
2) Quality Assurance – IPQA
- Designation: Officer/ Sr. Officer /Executive/ Sr. Executive
- Department : Quality Assurance – IPQA
- Qualification: B. Sc / M. Sc / B. Tech. (Biotech.) / M. Tech (Biotech)
- Total Experience: 01 to 05 years
Job Description:
- To perform line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labeling and packing.
- Environmental monitoring of manufacturing clean room area.
- Non-viable particle monitoring of manufacturing clean room area.
- Compressed air /nitrogen gas monitoring and Personnel monitoring.
- To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g. plates, swabs, etc.
- To perform Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP.
3) Quality Assurance – Validation
- Designation: Officer/ Sr. Officer /Executive/ Sr. Executive
- Department : Quality Assurance – Validation
- Qualification: B. Pharm / M. Pharm/ M. Sc /
- Total Experience: 01 to 07 years
Job Description:
- Execution and review of Qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant utilities
- Preparation and review of Validation/ Qualification protocol and report
- Preparation, review and execution of risk assessment activity related to equipment/ process/ facility/ system
- Conduct sampling activity as per the protocols (Process validation and clearing validation etc.)
- Assessment of Change Control, Deviation, CAPA, Investigation etc.
- Review of URS, DQ and vendor/ suppliers documents related to qualification
Note : Candidate should have 02 to 07 years 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 can register for interview online by submitting their details on given URL : https://forms.office.com/r/JmsLH4z4Vz
Candidates who are unable to attend interview, can share their CV on below mentioned email IDs: ajaykumar.pandey@amneal.com, or nechar.trivedi@amneal.com
