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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
careers@rpgls.com
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