- 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
- Customer Qualification – Perform customers qualified and Bonafides when required.
- Distribution – Assist in distribution issues and returns management from warehouses. Review and confirm Returns and RP/RPI checks delegated to 3rd LSP.
- 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.
- Quality experience within the industry, and application of Quality Systems & Quality Operations
- Minimum of 2-3 years' experience within the Pharmaceutical / Consumer Healthcare Industries, preferably in quality department, experience in a pharmaceutical manufacturing site is required.
- Knowledge of GMP and GDP regulations and MHRA/HPRA regulation
- Experience in importation/distribution of medicines in UK
- Degree of Pharmacy/Biology/Chemistry of similar
- Ability to work under pressure, prioritize and manage workload, manage simultaneous tasks, and meet deadlines in a changing, fast–paced environment
Quality Specialist - Weybridge, United Kingdom - Haleon
Description
Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. 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. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours.
Care to join us. It isn't a question.
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. It's an opportunity to be part of something special.
About the role
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:
This is hybrid role out of our offices in London and/or Weybridge (UK)
Qualifications and skills
Essential
Preferred
Care to join us. Find out what life at Haleon is really like
At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. 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. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
As you apply, we will ask you to share some personal information, which is entirely voluntary. 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. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.
Haleon is an Equal Opportunity Employer. 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.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements.