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Requirement of Quality Manager at RB’s health | M.Pharm, M.Sc

 

Clinical courses

RB is the world's leading consumer health and hygiene company. Every day, across 60 countries, we work with the best people to challenge conventional thinking and strive to find even better ways to give people innovative solutions for healthier lives and happier homes. We trust people in what they do and we give full accountability and autonomy to make things happen. That’s how we generate the game-changing ideas that built 19 iconic Powerbrands around the world, such as Mucinex, Lysol, MegaRed, Finish and Airwick.

Post : Quality Manager (Healthcare Manufacturing Facility)

SUMMARY OF ROLE
The overall purpose of the job is to guarantee and improve the quality of Reckitt- Benckiser products leaving the factory by leading the conceptualizing, implementing, improving and auditing the most economically efficient Quality system, in line with Global Quality Policy/Manual, the Global, Regional and local procedures and the particular requirements from Schedule M, WHO, MHRA, EU, USFDA and any regulatory authority.

Job Description

  • Ensure continuous improvement of site quality system as per the requirement of Domestic MHRA, EU, USFDA and other regulatory authority.
  • Guarantee, monitor, and improve Quality performance of manufacturing site.
  • Promote Quality attitude, awareness and mind set of the site by all proper means including training.
  • Implement, audit and develop quality system, in line with Global Quality policy/manual and the procedure relevant to area.
  • Lead and manage the local quality team.
  • Systematically reduce the cost of quality within the business while maintaining agreed quality standards.
  • Guarantee the conformances of products with agreed specifications.
  • Ensure necessary process controls are in place, including hand-over from R&D for new & existing developments.
  • Ensure consumer safety and company compliance with regulation.
  • Provide appropriate support in managing co-packers.
  • Manage customer complaint handling system to ensure that all complaints those related to quality of product are investigated timely and provided proper corrective and preventive actions.

 

Candidate Profile
- M.Sc. Chemistry or M. Pharma
- 15 years of work experience in Pharmaceutical Industry-   
- Familiar with GMP of pharmaceutical products, regulations and regulatory guidelines
- Experience in Handling of regulatory audits like MHRA, USFDA, MCC, ANVISA, WHO etc.

Additional Information:
Qualification : M. Pharm / M.Sc.
Industry Type: Pharma/ Biotech/Clinical Research
Location: India  
Functional Area: Healthcare Manufacturing Facility

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