65 Openings: Amneal Pharmaceuticals walk-in From 10th July – 11th July 2021

Amneal Pharmaceuticals is conducting Walk in drive From 10th July – 11th July 2021 For Officer/Sr. Officer/Executive.Amneal Pharmaceuticals, Inc. is an American publicly traded generics and specialty pharmaceutical company. The company is headquartered in Bridgewater, New Jersey. . Interested and eligible candidates can attend interview on scheduled time and venue. 

Walk in Details :

  • Company Name: Amneal Pharmaceuticals
  • Location: Kadi, Ahmedabad( Bavla, Changodar, Moraiya, Sachana )
  • Post Name: Officer/Sr. Officer/Executive
  • Qualification: M. Pharm/ B.Pharm/ Diploma Engineering/ D. Pharm/ B.Sc/ ITI
  • Experience: 2 – 5 years
  • No of Vacancies: 65
  • Details of Salary: NA
  • Time and Venue : 10th July – 11th July , 9.00 AM – 3.00 PM
    Hotel Papaya Tree A.B. Road, Indore Mega City Circle, Indore, Madhya Pradesh 453331 (view on Map)
  • Contact :  Neha Modi  ,  chandanid@amnealindia.com
  • Selection Process: Based on interview 

Job Description/Skills Required.


Sterile Manufacturing ( Injectable unit /Parenteral Unit)
JOB location: SEZ Matoda & Palli (Sachana Kadi)
Designation: Executive/ Officer/ Operators/ FTE
Qualification: M. Pharm/ B.Pharm/ Diploma Engineering/ D. Pharm/ B.Sc/ ITI
Total Experience: 02 to 07 years
Area: Aseptic & Controlled area operation (Filling, Sealing, filtration, intervention, Bag Printing, Production QMS, Autoclave, Batch Manufacturing, terminal sterilization etc)

Line: Ophthalmic, Vial, PFS & LYO, BAG & Ophthalmic

Positions: (50)

Officer/Executive – SEZ & PALLI : 40

Operator – SEZ : 10

Desired Profile:

  • To observe & follow all rules and regulations of the production department.
  • Must be from Parenteral background with exposure to Bag & vial filling process.
  • To be aware and responsible for achieving quality objective and fulfilling the requirements of the quality of the company’s service by means of applicable quality procedures.
  • Sound technical knowledge of Aseptic area and controlled are related activities.
  • Technical exposure and expertise on filling & Autoclave machine.
  • Knowledge of Regulatory guidelines and exposure of USFDA audits.
  • Knowledge of Quality Management System (QMS) i.e. 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.
  • BMR-BPR review

2. Quality Control- (Injectable unit /Parenteral Unit)

Location: SEZ Matoda

Designation: Officer/Sr. Officer/Executive
Qualification: M.sc Chemistry/ B.pharm/ M.pharm
Total experience: 02 to 05 years

Positions: 15

Area: RMPM, FP, IP, GLP, IR, UV, QC, Calibration, HPLC, LIMS, Stability, Analysis, Testing, QMS etc,.

Desired Profile:

  • Testing of raw material, packing material, in-process, finished product and stability samples (as per stability protocol).
  • To keep neat and cleanliness at work place and follow the Good laboratory practices in the laboratory.
  • To keep update of instrument slog-books and to record the data in LNB during testing. To attain and complete self-training record.
  • To initiate and review of A)Deviation B)Out of specification/Out of trend C)Change control
  • To ensure in and out of stability samples from stability chambers.
  • Charging of stability samples as per stability protocol.
  • To perform water analysis as per specification, SOP and GTP.
  • To co-ordinate QA for documentation for issuance and retrievals.
  • Review and monitoring of USP, EP, BP and other pharmacopeia monographs for changes/ revision.
  • To prepare COA of various product/material as per requirement whenever required.
  • LIMS master preparation for various product / material/ instruments/ Volumetric solutions etc.
  • Registration of reference standard, working standard, column, instrument etc. in LIMS
  • Preparation/updating of calibration schedule in LIMS
  • Updating of LIMS master as and when required
  • Preparation of configured Test plan.
  • Trouble shooting in LIMS, Involve in Qualification of LIMS module/ Instrument, Preparation of LIMS related protocol study and execution.

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