HomeProductionExecutive - Corporate Quality | RPG Lifesciences | Navi Mumbai

Executive – Corporate Quality | RPG Lifesciences | Navi Mumbai


RPG Life Sciences is certified as
One of India’s 100 Best Companies to Work For 2020 & One of India’s Best Workplaces in Biotechnology & Pharmaceuticals by
Great Place to Work® Institute

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We are proud and delighted to share that we have been ranked 85 amongst India’s 100 Best Companies to Work for 2020 by the Great Place to Work® Institute. We have excelled in the 5 dimensions that are a hallmark of a High-Trust, High-Performance Culture™ – Credibility, Respect, Fairness, Pride, and Camaraderie. Great Place to Work® is considered the ‘Gold Standard’ in workplace culture assessment and recognition.

Designation: Executive Corporate Quality

Location: Navi Mumbai, Maharashtra, India

Job description

  • Familiarity with incoming, in-process, and final testing procedures as well as demonstrating hands-on experience using a wide range of compendial procedures.
  • Familiar with FDA Quality System Regulations, GMP’s and/or other international regulations along with Drugs and Cosmetic Acts
  • Computer skills including those associated with word processing, spreadsheet programs, databases, and statistical analysis.
  • Perform data entry review and participate in an audit of CMO sites for a different formulation
  • Ability to prepare protocols and reports, operating documents, and procedures.
  • Ability to work with little or no supervision and make effective decisions in absence of superiors
  • Ability to communicate effectively and follow detailed written and verbal instructions.
  • Cooperate with coworkers within an organized team environment or work alone without supervision.
  • Manage time effectively to complete assignments in the expected time frame.
  • Knowledge of quality systems, quality techniques, current regulatory requirements, and technical issues resolution.

  • Review of Batch documents, Artwork profile, stability testing, etc
  • Complete all documentation with clear and accurate language and according to the Standard Operating Procedures.
  • Provide clearly written technical documentation.
  • Work with various teams to correctly identify root/probable causes and develop appropriate corrective/preventive actions to eliminate/mitigate the issue.
  • Revise related SOPs with the guidance of the CQ Head /Designee.
  • Must be familiar/experienced auditing techniques of six systems as per cGMP.

Qualification: B.Sc/B.Pharma, MS/M.Sc/M.Pharma

Experience: 2-5 Years

Salary: Negotiable

Contact Details:

Ms. Pranita Padte


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