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Freshers & Experience: Multiple Openings At Piramal Enterprises

Piramal Enterprises is Hiring for Senior Research Associate- ADL,Apprentice,Executive – Engineering,Manager – Quality Compliance,Production Executive, Senior Research Associate and has issued notification to accept Applications.Piramal Enterprises Limited is the Contract Development and Manufacturing Organisation (CDMO) business division of Piramal Enterprises Limited, with operations in North America, Europe and Asia. A global leader in integrated solutions, it offers a comprehensive range of services across the drug life cycle from drug discovery services and development to commercial manufacturing of drug substances and drug products. With accreditations from regulatory bodies in the US, Europe & Japan, its development centres and manufacturing sites across the globe, committed to research and development programs.. Interested and eligible candidates required to fill  application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Senior Research Associate- ADL,Apprentice,Executive – Engineering,Manager – Quality Compliance,Production Executive, Senior Research Associate as follows.

Vacancy summary details :

  • Company Name: Piramal Enterprises
  • Location : India-MADHYA PRADESH,GUJARAT,Maharashtra
  • Post Name: Senior Research Associate- ADL,Apprentice,Executive – Engineering,Manager – Quality Compliance,Production Executive, Senior Research Associate
  • Qualification:  M.Pharm,BE,M.sc,B.pharm
  • No of Vacancies: NA
  • Details of Salary: NA
  • Closing date for online Application : Apply as soon as possible
  • Mode of application : online
  • Selection Process: Shortlisted candidates may called for selection process (  Personal interview , Group discussion , etc…,)

Job Description/Skills Required: 

Apprentice  (210000XG)
Descriptio
  • To perform calibration of the analytical instruments as per calibration schedule.
  • Follow the standard practices- CGLP during Lab experiments.
  • Maintain hygienic condition in respective department.
  • Cleaning verification method development and Validation
  • API method evaluation and verification.
  • Following in-house compliance system.
  • Working standard qualification
  • Method development for drug product formulation
  • Routine analysis of development samples and lab stability samples.
  • Method verification and different analytical methods.
  • Preparation of test procedures for routine development analysis.
Senior Research Associate- ADL  (2100011W)
Description
  1. Analysis of Raw material and Packaging material.
  2. Calibration and maintenance of analytical instruments.
  3. Method development and validation of different drug product.
  4. Routine analysis of development samples and lab stability samples.
  5. GMP batch analysis and reporting.
  6. Stability batch analysis and reporting.
  7. Validation of Analytical methods.
  8. Follow GxP (GMP, GDP etc) for all processes.
  9. Following in-house compliance systems.
  10. Maintenance and calibration of Analytical instruments.
  11. Maintain hygienic condition in respective department.
  12. Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements.

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