Amneal Pharmaceuticals Ltd - Walk-Ins for Multiple Positions (80 Openings) in Manufacturing / QC / QC-Microbiology / QA / AR&D / F&D on 25th Oct' 2020 - PHARMA WISDOM

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Wednesday, 21 October 2020

Amneal Pharmaceuticals Ltd - Walk-Ins for Multiple Positions (80 Openings) in Manufacturing / QC / QC-Microbiology / QA / AR&D / F&D on 25th Oct' 2020

 

Amneal Injectable Walk-in Interviews on 25-Oct-20

Openings: 80

Date: 25 October, 9.00 AM - 1.00 PM

Venue:

Amneal Pharmaceuticals Pvt. Ltd.

Plot No 15, 16, 17 Pharmez Village: Matoda

Sarkhej Bavla Road,

Ahmedabad : 382213

 

We are looking for competent, dynamic and motivated candidates for suitable positions for Injectable unit for our Ahmedabad SEZ Matoda & Sachana Plant.

Note:

  • Mask will be mandatory for all
  • Do not attend interview if suffering from any health issue (cold, Cough, fever or Sore Throat)

Sterile Manufacturing ( Injectable unit /Parenteral Unit)
JOB location: SEZ Matoda
Designation: Sr. Officer/ Officer/ Operators
Qualification: B.Pharm/ Diploma Engineering/ D. Pharm/ B.Sc/ ITI
Total Experience: 02 to 07 years
Area: Aseptic and Control area (Filling, Documentation, CIP, SIP, autoclave, Batch Manufacturing)

Line: Ophthalmic

Positions: Officer-13 & Operator-30

JD:

  • To observe & follow all rules and regulations of the production department.
  • Must be from Parenteral background
  • 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 Eye drop filling machine and related batch mfg. process.
  • 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.
  • Preferred Exposure for Ophthalmic line: Three piece sterile eye drop filling machine operation (groninger), Nanomill Operation, autoclave (Fedegari) Manufacturing and Filtration vessel operation, CIP and SIP processing

Quality (Injectable unit /Parenteral Unit)
JOB location: Palli (Sachana-Kadi)
Designation: Sr. Executive/Executive/Sr. Officer/ Officer
Qualification: M. Pharm/ B.Pharm/ M.Sc
Total Experience: 02 to 07 years
Area: Quality Control, Quality Control Microbiology and Quality Assurance

Line: Bag Line

Positions: 21

JD:

Quality Control (Bag Line)

Position: 9

  • GLP Activities, Calibration, LIMS
  • Various Analysis (Raw Material Analysis, Finished Product Analysis, In process Sample Analysis, Cleaning Validation Sample Analysis, Water Sample Analysis, Stability Sample Analysis, In-Use study Analysis
  • Freeze through Study & Thermal Cycle Study
  • Data Reviewer, QMS (OOS, OOT, CAPA, Change control Etc,.
  • Stability Chamber and Sample management
  • Reagent Management

Quality Assurance (Bag Line)

Position: 8

  • IPQA (Line clearance, BMR-BPR review, Sample collection, In process check, Dispensing, Etc)
  • Validation Activities (SOP preparations, Initial & periodically Validation, qualification of utilities and Equipment, Cleaning Validation, Process Validation, Validation Master plan, etc.,)
  • QMS Activities (Handling of Deviation, CAPA, Incident, etc)
  • Doc cell Activities (Manual Issuance, Retrieval, SOP preparation, review, etc)

Quality Control Microbiology (Bag Line)

Position: 4

  • Microbiological testing Activities ( Media Preparation & discard, Growth Promotion test, Autoclave operation, Culture handling, Equipment calibration & qualification, , Micro Lab routing documentation, Disinfection Study, etc)
  • GLP, Media & Review : Activities (Sterility Testing, BET testing, Bioburden Analysis, Water sampling & analysis, Method validation / Qualification, Personal Monitoring, etc)
  • Documentations (SOP Preparation, Study Protocols Preparation, Study Report Preparation, Method Validation Protocol and reports, etc)
  • Environmental Monitoring (Settle plate exposure, Microbial air sampling, Surface sampling, Particle count (NVPC), Media plate observation)

For Injectable, if you are unable to attend interview you can share cv on neha.modi@amnealindia.com

We are also having requirements for Manufacturing (OSD), AR&D (OSD) and F&D(OSD). Interested candidates may either submit hardcopy of their CV at venue, or mail CV on chandanid@amnealindia.com & kishan.soni@amnealindia.com Candidates with suitable profile will be scheduled for interview separately.

Required Candidate profile

The candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP/ GLP Knowledge and understanding of regulatory requirement is essential.

Note :

  • Candidate should have 02 to 07 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organisation.
  • You may walk in for interview with current CV along with CTC proof Appointment letter, Increment letter & last 3 months salary slip & Bank statement, Aadhar & PAN card and 2 passport size photograph.
  • Those who have already attended interview in last 6 month need not appear again for interview

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