Senior Quality Associate
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
Your responsibilities
• Line management of Quality Associates and ownership of related activities. Delegating tasks effectively to ensure that products in the external manufacturing portfolio are compliant to Regulatory and Reckitt standards.
• Coach and develop Quality Associates to strengthen individual capabilities and build a high performing, engaged team.
• Identity development needs and implement tailored development plans to grow technical and leadership skills across the Quality Associates.
• Promote cross-functional collaboration, communication and knowledge sharing among the team and stakeholders.
• Act as Quality approver and/or support as SME for QMS records owned by Quality Associates, ensuring decisions are aligned with quality standards and business priorities.
• Ensuring that auditor competency is sufficient for the scope of products and relevant classifications for own and Quality Associates portfolio management.
• Actively engage in Quality Improvement plans and support their execution.
• Act as a lead auditor to assess and approve external manufacturers with ongoing management of a defined portfolio.
• Review Product Quality Reviews where it is applicable according to product classifications and Technical Agreement and ensures that product meets with Reckitt requirements
The experience we're looking for
• Excellent risk management skills to identify and mitigate supplier risks to the business, developing strategies and executing action plans to resolve critical issues.
• Proven leadership skills with prior experience in people management.
• Experience managing third-party manufacturing operations.
• Technical and professional qualifications, including experience in quality audit.
• Thorough knowledge on the regulatory requirements, rules and guidance covering the QMS and manufacture of pharmaceutical products in Europe, such as EU GMP/GDP, ISO13485 and ISO22716.
• Degree in Chemistry, Chemical Engineering or Pharmaceutics.
• Experience of working in a quality function in Healthcare, Pharmaceutical, or Medical Device related industry.
• Travel will be required in Europe / UK.
The skills for success
What we offer
Equality
                
                
                    
                    
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