Regulatory affairs jobs in Horley

A rare opportunity to join a well-known chemical products company as Chemical Regulatory Affairs Manager. We are looking for previous chemical regulatory experience, ideally some leadership/supervision, excellent communication skills and the ability to communicate the complex word of chemical reg...

Premier Work Support are excited to be recruiting for a Regulatory Affairs Product Manager for a prestigious Manufacturing client based in Tadworth . This role will be working on all sectors (Family ...

Premier Work Support are excited to be recruiting for a Regulatory Affairs Associate for a prestigious Manufacturing client based in Tadworth . This is a 6 month fixed contract. This role will be ...

SRG are currently looking for a Regulatory Affairs Associate for a Global Healthcare Company who have opened a new vacancy within their Regulatory team on an initial 6-month basis based out of their ...

A rare opportunity to join a well-known chemical products company as Chemical Regulatory Affairs Manager. We are looking for previous chemical regulatory experience, ideally some leadership ...

Quality Assurance and Regulatory Affairs (QARA): * Uphold full compliance with all regulatory standards within the department. Health & Safety: * Foster a robust health and safety culture across the ...

... public affairs, health and value, communications, legal, compliance, quality, regulatory, commercial and supply, working with the Glocal commercial teams to maximise UK approach. Roles ...

... relevant regulations. * Taxation: Providing tax planning advice and ensuring clients' tax ... Experience in providing tax advice and managing clients' tax affairs. * Excellent communication ...

Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to suppo...

This is an exciting opportunity to join a Global Regulatory Affairs team to develop and implement global regulatory strategic and leadership of regulatory activities for product development. Must have hands-on knowledge of pediatric regulatory requirements, including ICH requirements and regional...

As a CMC Regulatory Affairs Manager, you will manage the production of Chemistry, Manufacturing and Control (CMC) documentation for designated product ranges. You will manage global CMC regulatory submissions ensuring that project activities and documentation are delivered to the required standar...

Works with the Lead, Regulatory Affairs, and the Development Team, and with moderate/minimal supervision, with select project teams within subsidiary organizations to develop and oversee program-specific regulatory, clinical, and development strategies. Responsible, with direction from Lead, Regu...

Reporting to the Chief Regulatory Officer, this role will be responsible for all regulatory activities for medical device and combination products, including defining the device regulatory strategy and overseeing all device submissions across global markets. Device Regulatory Affairs, Senior Dire...

Provide regulatory affairs expertise to clients seeking regulatory strategic input to their development programmes. Senior/Executive Director of Regulatory Affairs. Solid understanding of Regulatory Life Cycle Management and eCTD format for regulatory filings. Applies senior regulatory affairs ex...

With broad and comprehensive expertise within the Regulatory environment you will lead project work and partner with the business to solve complex regulatory issues that impact the department or wider business. Support external regulatory agency audits, providing regulatory input to minimize pote...

Expertise in authoring and reviewing of regulatory documents; development regulatory documents; Regulatory Strategy Plans, Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Orphan Drug and Paediatric plans/applicati...

Provide high level strategic and operational regulatory direction and mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approvals in international markets, regulatory strategic development plans and risk ...

This is a key new hire within the Scientific and Regulatory Affairs team – you will provide regulatory support to the chemicals management and Government and Public Affairs team. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, R...

Senior Regulatory Affairs Specialist who will be responsible for planning, creating, and implementing solutions for regulatory registration and release of products for distribution into specific geographies. Senior Regulatory Affairs Specialist – Medical Devices & IVD’s. Minimum of 4 to 5 years p...

Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...

Regulatory Affairs Associate Manager - Cosmetics. Planet Pharma are partnered with a niche mid-sized CRO assisting them with the search for an Associate Manager, Regulatory Affairs to work on an initial 6+ month project with a focus on Cosmetic products. Minimum of 3+ years of experience in regul...

Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Main...

May write new regulatory SOPs and regulatory intelligence databanks, and/or propose revisions and/or act as reviewer for regulatory SOPs, as assigned and appropriate. Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for ...

Regulatory Affairs Director | Associate Regulatory Affairs Director Europe | EU | EMEA | Head of Regulatory Affairs | Regulatory Affairs Director Europe | Pharmaceutical | Biologics | Biopharmaceutical. The Regulatory Affairs Director, Europe will drive regional strategy and deliver hands-on regu...