Regulatory affairs jobs in SaleCreate job alerts

We’re Hiring: Team Leader – Regulatory Affairs (IVD). A growing diagnostics innovator is building out its UK-based Regulatory Affairs team and looking for a. You’ll lead a small team (including RA officers and admin staff), take ownership of regulatory input into product changes and compliance

Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment. Advise internal stakeholders on regulatory risks and compliance. Represent the company in external regulatory forums and industry groups.

Department Leader – Regulatory Affairs– IVDs. An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department. The Department Leader for Regulatory Affairs is also responsible for acting as an active participant in team meetings tha

The role will involve regulatory assessment, compliance review and documentation management to ensure cosmetic products meet the necessary legislation and safety standards in multiple territories, including the UK, EU, US and Canada. Conduct regulatory reviews of formulations, labelling, and pack...

Experience : 5 years in Medicinal Products Regulatory Affairs with 2 years in Project Management. Experience working with Microsoft Project or equivalent program (.

This is a fantastic opportunity for someone with a strong background in regulatory documentation—particularly SmPCs, PILs, and labelling compliance—to join a high-performing regulatory affairs team. Walker Cole are partnered with a leading pharmaceutical company in the UK that is looking to brin

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. If you would like to discuss this vacancy further or to discuss your career options in confidence, ple...

Lead a multidisciplinary labeling working group and provide labeling strategy proposal (Global Regulatory Affairs, Global Pharmacovigilance, Global Medical Affairs, Legal, Communication, preclinical and CMC…). Bachelor’s degree, in scientific discipline, or relevant/equivalent with more years of

The role will involve regulatory assessment, compliance review and documentation management to ensure cosmetic products meet the necessary legislation and safety standards in multiple territories, including the UK, EU, US and Canada. Conduct regulatory reviews of formulations, labelling, and pack...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. This position will play a crucial role in ensuring the integ...

Other suitable skills and experience include Quality Assurance Manager, Regulatory Affairs Specialist, QA/RA Manager, Medical Device Auditor, Quality Systems Specialist, Compliance Officer, Risk Management Specialist #J-18808-Ljbffr. Senior Quality Assurance & Regulatory Affairs Specialist to. Se...

Senior Quality Assurance & Regulatory Affairs Specialist!. Senior Quality Assurance & Regulatory Affairs Specialist to.

Open Position The Head, Global Scientific and Regulatory Affairs (GSRA), Europe Middle East & Africa (EMEA) Region, is the regional lead responsible for providing leadership and direction to the scientific and regulatory function in the region. Minimum 10+ year experience in regulatory affairs wi...

Job DescriptionJob Description JOB SUMMARY: The Quality Systems Manager will provide overall company leadership and direction for Quality Assurance and Regulatory Affairs Systems, encompassing both improvements and sustaining activities. Enhance company systems interface capabilities while optimi...

Managing Partner- Medical Communications VML Department: Medical & Scientific Expertise: Health Location: Last Updated: 4/16/2025 Requisition ID: 9551 Who We Are: At VML, we are a beacon of innovation and growth in an ever-evolving world. Our heritage is built upon a century of combined expertise...

As Head of Regulatory Affairs, you will: Lead the Regulatory Affairs team Oversight of license compliance with MHRA Submit new MAA / licenses variations to regulatory authority Act as point of contact for the company with the MHRA, external stakeholders and license users Assist in the training an...

Ideas | People | Trust We’re BDO. An accountancy and business advisory firm, providing the advice and solutions businesses need to navigate today’s changing world. We’ll broaden your horizons Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. They...

Social network you want to login/join with: We are seeking an experienced and driven Senior PK/PD Modeller to join our Clinical Pharmacology team. In this role, you will be responsible for the design, development, and implementation of pharmacokinetic/pharmacodynamic (PK/PD) modeling strategies...

Meet all quality, quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Show constant attention to detail, and immediately inform supervisor of anything out of the ordinary, or anything which does not conform to the approved process sheets. Work with E...

Social network you want to login/join with: Job Title: Customer & Market Insights Innovation Lead Location: Reading - Awaiting confirmation on any onsite requirements Sector: Global Biotech FTE: 3 days per week (may flex to 4/5 during busy periods if possible) Role Summary We’re looking fo...

Social network you want to login/join with: Are you an experienced QA/RA leader ready to shape the future of wound care? A pioneering MedTech start-up is seeking a Quality Assurance and Regulatory Affairs Manager to drive global regulatory strategy and quality systems for an innovative Advanced...

Title: QA Officer - Clinical Location: Greater Manchester Salary: 41,000 About the Role SRG are recruiting for a QA Officer with GcP experience to join an innovative company whose technologies form an integral to the advancement of Life science & Healthcare research all over the world. Based at ...

Title: QA Officer - Clinical Location: Greater Manchester Salary: £41,000 About the Role SRG is recruiting for a QA Officer with GCP experience to join an innovative company whose technologies are integral to the advancement of life science and healthcare research worldwide. Based at their si...

Arxada is a global specialty chemicals business that’s committed to solving the world’s toughest preservation challenges through better science. We aim to help our customers develop more sustainable solutions that protect and maintain the health and wellbeing of people and extend the life of vit...

Senior Vice President / Vice President of Regulatory Affairs. Senior Vice President / Vice President of Regulatory Affairs. This executive role will lead global regulatory strategy, with a particular focus on the UK and EU, supporting the development of advanced genetic therapies using ASO techno...

Sr. Director, Regulatory Affairs - CMC LinkedIn Twitter Email Message Share CMC / Technical Operations Cambridge, MA * ID: 25R-19 - Full-Time/Regular Nearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. At Akebia we take that number very ser...

Social network you want to login/join with: col-narrow-left Cpl Life Sciences manchester, United Kingdom Other - Yes col-narrow-right 5 26.06.2025 10.08.2025 col-wide Job Title: Department Leader – Regulatory Affairs– IVDs Job Type: Full-Time, permanent position Location: Outskirts...

Sr. Director, Regulatory Affairs LinkedIn Twitter Email Message Share Regulatory Affairs Cambridge, MA * ID: 25A-15 - Full-Time/Regular Nearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. At Akebia we take that number very seriously and eve...

JOB TITLE: Head, Global Scientific and Regulatory Affairs (GSRA), EMEA Region LOCATION: UK. Manchester Head Office. REPORTS TO: Vice President, Global Scientific and Regulatory Affairs, located at the Ingredion Innovation Center, New Jersey, USA DIRECT REPORTS: Yes - three Company Background...

Social network you want to login/join with: col-narrow-left Ramboll Manchester, United Kingdom Other - Yes col-narrow-right 7b74e4929e42 3 29.06.2025 13.08.2025 col-wide Job Description Location: United Kingdom (any Ramboll office), Germany (Munich, Frankfurt, Bad Kreuznach, Berli...

Birmingham, England, United Kingdom; Glasgow, Scotland, United Kingdom; London, England, United Kingdom; Manchester, England, United Kingdom; Remote; UK Company Overview Throughout our worldwide network of experts, clients and communities, we are renowned for our leadership in fire protection ...

Social network you want to login/join with: - Coordinates, provides, and delivers methodological and statistical expertise and/or statistical analyses. Supports both the Clinical Development portfolio and Strategic Medical Affairs in their support to Affiliates, complying with international, r...

Ideas | People | Trust We’re BDO. An accountancy and business advisory firm, providing the advice and solutions businesses need to navigate today’s changing world. We’ll broaden your horizons Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. They...

Social network you want to login/join with: Client: Gazprom Energy Location: Manchester, United Kingdom Job Category: Other EU work permit required: Yes Job Reference: dabfca5011b9 Job Views: 48 Posted: 24.06.2025 We’re looking to build on over 20 years of experience in the gas, power, a...

Join to apply for the Senior Consultant - SDS Author role at Ricardo plc Continue with Google Continue with Google 3 days ago Be among the first 25 applicants Join to apply for the Senior Consultant - SDS Author role at Ricardo plc Get AI-powered advice on this job and more exclusive feature...

- Responsibilities: You will work on projects that involve the detailed analysis and presentation of data from clinical trials, which are instrumental to the successful uptake of novel therapies - Salary: £39,000 per annum (please note that we have established salary bands that are determined ...

At the core of Epic’s success are talented, passionate people. Epic prides itself on creating a collaborative, welcoming, and creative environment. Whether it’s building award-winning games or crafting engine technology that enables others to make visually stunning interactive experiences, we’re...

This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. Overview At the heart of QIAGEN's business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the en...

Salary: GBP35000 - GBP35000 per annum Specification Technologist – 12-Month Fixed Term Contract Are you an experienced Specification Technologist with a keen eye for detail? We’re looking for someone to join our team on a 12-month fixed-term contract . In this role, you'll ensure that product ...

Social network you want to login/join with: - Being part of an international company yet with local presence - Build a safer digital society together with us Orange Cyberdefense is the expert cyber security business unit of the Orange Group, providing security consulting, solutions and servic...

Who We Are: At VML, we are a beacon of innovation and growth in an ever-evolving world. Our heritage is built upon a century of combined expertise, where creativity meets technology, and diverse perspectives ignite inspiration. With the merger of VMLY&R and Wunderman Thompson, we have forged a n...

Social network you want to login/join with: An excellent opportunity for an experience Medical Information Manager to join a well established Pharma company in Berkshire . The Medical Information Manager provides accurate, unbiased, balanced, and timely responses to unsolicited medical and clin...

Collaborative Approach and Stakeholder Engagement Work closely with the Legal & Public Affairs team, as well as key stakeholders across the Trips business, to ensure effective collaboration and technical support for various projects. Develop and deliver training materials and guidance documents f...

Social network you want to login/join with: Regulatory Affairs Manager - Pharmaceuticals As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. Additionally, you w...

Job Description Regulatory Officer £35,000+ dependent on experience Manchester Blush & Bloom are working on an exciting opportunity with a well-established and highly reputable business in the cosmetics and personal care industry. Due to continued growth, this organisation are seeking a Regulat

Our client who is developing an advanced and innovative wound dressing platform (Advanced Tissue Repair Platform) to substantially, will improve the clinical outcome for patients with Chronic and Complex Wounds whilst maintaining simplicity for care providers. Our Client is on a mission to i...

Senior Vice President / Vice President of Regulatory Affairs. Lead regulatory strategy and submissions across the UK, EU, and potentially the US. Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment.

The Department Leader for Regulatory Affairs is also responsible for acting as an active participant in team meetings that relate to changes to developed products that will require further registration and regulatory submissions. The Department Leader is also responsible for managing and supporti...