Quality Manager - Pharma Channel FRBNL

<h2>We are Reckitt</h2> Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.<h2>​Research &amp; Development​</h2> In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.<br/> <br/> 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.<br/> <br/> The size of our organisation means you'll have the opportunity to learn and work in different functions within R&amp;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.<h2>About the role</h2> <p>The primary responsibility of the Quality Manager (Health) is to provide leadership for excellence in Quality and Compliance of all Health products and processes within the supply/distribution chain, including embellishment. The QM will: lead and facilitate quality continuous improvement activities; assure proper quality systems are developed to comply with current regulations such as relevant GMP and GDP; implement processes and procedures and observe/audit for compliance; establish objectives for Quality improvement within the region; provide feedback to the region on performance against relevant internal and external quality, regulatory/statutory requirements; serve as a resource for information relative to all aspects of products and process quality; facilitate the ‘right first time’ approach and implementation of new products and processes; and support and integrate continuous improvement principles within the region through proactive  communication, partnering, training and education. </p> <p> </p> <p>This position is responsible for ensuring that the region maintains compliance with applicable regulations as appropriate while also supporting and enabling the business to achieve its business objectives. The Quality Manager (Health) must work effectively with internal parties, manufacturing sites, third parties, external bodies and corporate personnel. </p><h2>Your responsibilities</h2> <ul> <li>Responsible for supporting the GM’s and their management teams to enable them to develop and implement the local Quality Management System (QMS) to ensure fully compliant products. </li> <li>Provide leadership on continuous improvement projects, quality initiatives, etc. as established by corporate Quality Management. </li> <li>Work with local functions to develop and maintain all relevant procedures in line with the requirements of the Global BMS &amp; associated policies, relevant codes of practice and GDP. </li> <li>Ensure that the QMS is maintained in a state of inspection readiness. </li> <li>Ensure a system is in place to manage local embellishment, re-pack, and co-packing work to meet all regulatory requirements. </li> <li>Change Management - Ensure a robust and effective change control system is in place to ensure business changes are effectively managed. </li> <li>Training – Ensure a training system for the business is in place and provide training on the local QMS. </li> <li>Issue Management - Investigate quality issues (Non-conformances) and failures (CEP Events) and apply Corrective and Preventive Actions (CAPA) to prevent recurrence. Advice regarding CAPA necessary at regional quality level for items not under local control. Ensure that improvements to products and procedures can be identified and fixed. </li> <li>Audit/Inspection Management – Ensure that processes are in place to assess the adequacy and effectiveness of the local QMS. Audit should cover all aspects of the BMS and local QMS to ensure compliance. Ensure a routine review program and audits are in place for Third Party providers</li> <li>Document Management – Maintain a document control system for the local QMS. Perform reviews and approve business procedures &amp; Technical Agreements. </li> <li>Product Recall - as per the Critical Quality Events and Product Recall procedure establish and communicate responsibilities. Conduct mock recall exercises to confirm adequacy of the local recall procedure. </li> <li>Maintain a Fit-For-Purpose QMS: Report level of compliance of local Q