Amneal Pharmaceuticals Pvt. Ltd Recruitment-Send Resume O HR mail

Amneal Pharmaceuticals Pvt. Ltd Walk-in Interview 2025.Amneal Pharmaceuticals Pvt. Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..

Vacancy details:

• Designation: Manufacturing & Packing (Tablet/Capsule)/Senior Officer, Analytical R&D Compliance
• Qualification: B. Pharm, ITI,Diploma,Any Graduate,Any Postgraduate
• Total Experience:02 to 06 years

Important Details :

• Work Location: Ahmedabad
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Job Description: Greeting from Amneal Pharmaceuticals Pvt. Ltd !!!

Hiring for Manufacturing (OSD) at Amneal Pharma for SEZ Matoda, Ahmedabad plant

(Oral Solid – OSD Requirement)

1.Manufacturing & Packing (Tablet/Capsule)

Requirement For Officers & Executives

Designation: Officer/ Sr. Officer /Executive

Qualification: B. Pharm, ITI,Diploma

Total Experience: 02 to 06 years

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, Auto coater, 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.

Interested candidate can share cv on chandanid@amneal.com with caption “CV for Production”

Senior Officer, Analytical R&D Compliance

1. To perform / review daily calibration of laboratory equipment, lamp energy check, time synchronization check, temperature monitoring and any compliance related activities.
2. To maintain laboratory equipment in proper operating condition and perform calibration as required, after completion allied training of sophisticated instruments i.e. UPLC, HPLC, GC, ICP-OES, ICP-MS, Dissolution Apparatus etc.
3. To deliver consistent and precise results by following safety and GXP protocols/ SOPs/ regulatory guidance.
4. To associate service/instrument engineer during routine preventive maintenance and troubleshooting/repair services on all laboratory equipment.
5. To establish, execute and evaluate laboratory instrument calibration procedures and policies.
6. To prepare qualification protocol / report and compliance documents.
7. To prepare and execute the Computer Systems Validation protocols and to make sure that all GxP computer-based systems are operating as intended and meet regulatory requirements.
8. To interact with Quality Assurance and service providers, other cross functional department related to CSV, Qualification and PM activity.
9. To prepare / revise Standard Operating Procedures, through change control procedure in accordance to regulatory guidance / reference documents.
10. To update lab compliance documentation system to exceed good laboratory practice, nearly meeting site GXP quality standard expectations.
11. To create, update, review and manage of Calibration, Preventive maintenance, and validation schedule.
12. To review Third-Party Documents / Certificate of Analysis.
13. To receive and manage controlled issued documents from QA Department.
14. Issuance of Laboratory notebook, Equipment logbook and Column usage registers.
15. To qualify in-house Working / Reference standard and impurities.