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Strong fit if you have senior quality/compliance experience in life sciences or similar regulated environments and prefer on-site UK work at a large scientific-tools company. Data here does not include salary bands, glassdoor-style reviews, or formal cert paths—treat those as open discovery in process.
As a Senior Quality Compliance Specialist at Thermo Fisher Scientific, a typical day centers on quality systems for regulated lab and manufacturing contexts: reviewing procedures and records against internal and external requirements, investigating deviations and CAPAs, supporting audits and inspections, and partnering with QA, operations, and product teams. Recent company emphasis on quality-assurance tooling and regulated products (e.g. forensic DNA workflows) implies close attention to documentation integrity, change control, and continuous improvement—not inventing product claims beyond public news.
No—the listing marks remote as off; expect UK-based on-site work.
Public items include quality-assurance software, Rapid DNA forensic approval, and a Middleton workforce reduction—use primary links above for detail.
No certification family or costed resources were provided for this occupation; confirm requirements with the employer.
Website: thermofisherscientific.com
Public cache only — not an employee review.
Senior Quality Compliance Specialist at Thermo Fisher Scientific in UK About the Role As a Senior Quality Compliance Specialist within our Clinical Trials Division (CTD) at Thermo Fisher Scientific, you will play a crucial role in ensuring that all clinical trials and related activities comply with regulatory requirements. This position is based in the UK and requires full-time commitment. Your Responsibilities Ensure compliance with local, national, and international regulations governing clinical trials. Develop, implement, and maintain quality systems to support clinical trial operations. Conduct audits and inspections to ensure adherence to regulatory standards. Collaborate with cross-functional teams to address any non-compliance issues promptly. Stay updated on changes in regulations and industry best practices. Who We're Looking For We are seeking a highly skilled and experienced Senior Quality Compliance Specialist who can contribute significantly to our mission of making the world healthier, cleaner, and safer. Key qualifications include: A minimum of 5 years of experience in quality compliance within clinical trials or pharmaceutical industry. Strong knowledge of GCP (Good Clinical Practice) and related regulations. Excellent communication and interpersonal skills to work effectively with various stakeholders. Ability to manage multiple projects simultaneously while maintaining high standards of quality. About the Company Thermo Fisher Scientific is a global leader in serving science, providing innovative technologies, workflows, and services that advance our understanding of the world. Our mission is to enable our customers to make the world healthier, cleaner, and safer through scientific discovery. Ready to Apply? To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. Join us in making a positive impact at Thermo Fisher Scientific!
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