- Batch Certification, Release to the Market and repacking activities - Support the batch assessment/release process within the regulatory and corporate framework to ensure timely release of products (medicines, and Mass market products) and timely review of PPR (PQR).
- Quality Agreements - support review and approval of Technical Terms of Supply or Quality Agreement when required.
- Management of 3rd Party Contractors - Provide support in third parties overview.
- Risk Management - Support Risk Management oversight for Quality and supply chain risks.
- Training - Assign trainings to relevant personnel, KPI monitoring and drive action plans when needed, ensure training matrix and curricula are maintained.
- QMS implementation - Support QMS implementation strategy, assist in documentation assessment, review and update in timely manner, and relevant personnel are assigned training.
- Complaint Management - Support the complaint process by ensuring the complaints raised are dealt with in timely manner and assist with trending.
- NPI - Support the New Product Introduction projects as per as Haleon procedure
- Others - Support the team in projects and day to day activities as required such as incident management, PIRC, Internal Audits, Quality Council and Quality team meetings.
- Minimum of 2-3 years' experience within the Pharmaceutical / Consumer Healthcare Industries, preferably in quality department, experience in a pharmaceutical manufacturing site is required.
- We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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Quality Specialist - Surrey, United Kingdom - Haleon
Description
A new world-leading consumer health company. Together, we're improving everyday health for billions of people.By growing and innovating our global portfolio of category-leading brands - including Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science.
With category leading brands such as Panadol, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business.
This is an exciting time to join us and help shape the future.As Quality Assurance Specialist, you will implement and maintain effective Quality Assurance systems to ensure that local operations are in full compliance with Haleon standards and policies, GMP, GDP and regulatory requirements by performing the following:
Quality experience within the industry, and application of Quality Systems & Quality Operations
