At a Glance
- Tasks: Ensure quality and compliance in manufacturing medical devices and cosmetics.
- Company: Dynamic company focused on regulated manufacturing in Folkestone.
- Benefits: Competitive pay, supportive work culture, and opportunities for growth.
- Other info: Safety-first environment with a commitment to diversity and inclusion.
- Why this job: Join a proactive team and make a real difference in product quality.
- Qualifications: Attention to detail, QA experience, and good IT skills required.
The predicted salary is between 33696 - 41184 £ per year.
Working hours: Mon-Thurs 08:00-16:30, Fri 08:00-15:30 (30 mins unpaid lunch daily)
Hands-on QA Operations role in regulated manufacturing, supporting medical devices and cosmetics at a busy Folkestone site.
About the role
Quality and compliance depend on strong GMP oversight at every stage.
In this hands-on position, you'll work across manufacturing and goods-in to ensure materials, documentation, and release decisions meet approved standards-helping drive a proactive quality culture on the shop floor and in the warehouse.
Key responsibilities
- Promote and embed GMP and a proactive quality culture across QA and Production.
- Carry out QA activities supporting the manufacture and distribution of medical devices and cosmetics.
- Inspect, sample and evaluate incoming components/packaging against approved specifications.
- Review, approve and release components and packaging materials in SAP (Systems, Applications and Products).
- Review batch records, manage discrepancies, and support batch/finished product release.
- Manage deviations, non-conformances and CAPAs (Corrective and Preventive Actions) via the Agile system, ensuring timely closure.
- Maintain compliant TQM (Total Quality Management)/GMP documentation and controlled records.
- Maintain reference samples and controlled artwork libraries; provide Certificates of Analysis (Co A) as required.
- Provide QA oversight at goods-in (including rejection labelling) and resolve issues cross-functionally.
Skills & experience
- Strong attention to detail and confident decision-making using data and evidence.
- Good IT skills (MS Word/Excel) and comfortable working with quality systems.
- Able to plan ahead, use initiative and respond positively to change.
- QA experience within a regulated industry (FMCG, medical devices, pharma, cosmetics).
- Knowledge of ISO 22716 and/or ISO 13485.
- Health & Safety & culture
Safety is a top priority; you must follow all site H&S procedures and report accidents/near misses.
All applicants will be assessed solely on suitability, without regard to age, gender, disability, ethnicity, religion, belief, or sexual orientation.
- Kent and Medway NHS and Social Care Partnership Trust
- #J-18808-Ljbffr
Product Compliance Specialist in Folkestone employer: Allscreens Nationwide Ltd
Allscreens Nationwide is an exceptional employer, offering a supportive team culture where employees are valued and encouraged to thrive. With access to state-of-the-art training facilities and opportunities for career progression, our Automotive Glazing Technicians in Birmingham can expect not only competitive bonuses but also the chance to work with the latest technology in the industry. Join us and be part of a company that prioritises both employee well-being and customer satisfaction.
StudySmarter Expert Advice🤫
We think this is how you could land Product Compliance Specialist in Folkestone
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We think you need these skills to ace Product Compliance Specialist in Folkestone
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Allscreens Nationwide Ltd!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Allscreens Nationwide Ltd that you're not just a fit for the job but also a safety-conscious candidate!
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Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Allscreens Nationwide Ltd, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Allscreens Nationwide Ltd
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Allscreens Nationwide Ltd that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Allscreens Nationwide Ltd’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
