Product Compliance Specialist

A collective energy and ambition. A place where you can make a real difference.

We’re a company that genuinely cares about our people, our products, our consumers and the environment.

Our unique, informal culture champions courage, determination and collaboration. Knowing we have an open and supportive team means each of us has the freedom to take responsibility and ownership. We have a shared passion to work hard, innovate and push boundaries.

United by the belief that when we strive for growth, anything is possible. While we might not be the largest company in our industry, we believe we can have the biggest impact because: Together We Have the Power to Win.

Do you have experience of managing GMP quality assurance tasks? Have you worked within a multinational fast-moving consumer goods, medical devices or pharma organisation?

If the answer is yes - then look no further as Church & Dwight UK Ltd have an exciting opportunity for a Product Compliance Specialist to join our team in Folkestone, Kent on a permanent basis.

The Product Compliance Specialist will be responsible for working alongside the manufacturing team on all GMP quality assurance tasks related to the production and distribution of goods.

Key Responsibilities include:
- To support and foster a Quality culture within the QA Ops team and the wider production environment- Packaging component & finished product specification management- Inspect incoming components and packaging components according to the relevant specifications, determining whether materials are fit for use- Maintain the specifications for all materials required for use in C&D UK Ltd- Maintaining the line complaint system and ensuring that follow ups are met to close these out- To provide Certificates of Analysis (CofA) for stakeholders when required for stock shipped- Work with internal stakeholders to ensure that all testing procedures are up to date and validated- Reporting and documenting on any non-conformances raised at goods in or online through the Agile system and completing the investigations to close out the non-conformances- To maintain accurate and true TQM records and to ensure that is complies to the relevant procedures and quality standards- To ensure that Production adhere to GMP through training, collaboration and inspection- Assist in the investigation of all adverse complaints received by C&D Europe relating to in-house produced Cosmetic and Medical device products- To work effectively cross functionally with key stakeholders in Production, Planning, Marketing and R&D- Maintain and report monthly RFT metrics and KPIs for in-house production, helping to drive improvements- Release of Finished Product- Supports the plant, QA Office and Laboratory 5S programmes- Have proven experience working in a Quality Assurance role within a regulated industry (e.g. MFCG, Medical Device, Pharmaceuticals) is desirable but not essential- Have an education in a science or engineering-based arena- Be accurate with excellent attention to detail- Have a working knowledge of ISO22716 and or ISO13485 is desirable- Be computer literate with MS Word and Excel- Be self-motivated with the ability to plan ahead and use initiative- Have the ability to analyse and interpret data to make accurate and expedient decisions- Be able to foster strong Multi-functional relationships- Be able to respond positively to change

In return we offer a competitive package, including 24 days annual leave, a pension matched up to 9%, discretionary annual bonus, life assurance cover and membership of a health cash plan.

For more information on our company, our brands and our culture visit us at

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