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Partnering with an international pharmaceutical company focused on both in house product development and CDMO services, we are now supporting the appointment of a new Regulatory CMC Project Manager to oversee regulatory activities for a small molecule oncology product globally. Experience in pre-...

Evaluate data from standard regulatory studies Assess the human health hazards of a variety of chemicals To be considered as a Toxicology Regulatory Scientist, you will need: A degree (minimum 2:2), ideally a postgraduate qualification, in a relevant science subject, such as Toxicology, Pharma...

Fascinating opportunity for you as a German speaking Regulatory Manager to work across multiple EU markets. This global food business is looking for a Regulatory Manager to help them as they grow closer collaboration through their EU businesses. All they ask for is you have food regulatory experi...

Evaluate data from standard regulatory studies Assess the human health hazards of a variety of chemicals To be considered as a Toxicology Regulatory Scientist, you will need: A degree (minimum 2:2), ideally a postgraduate qualification, in a relevant science subject, such as Toxicology, Pharma...

Reporting directly to the Global Head of Regulatory, you will play a pivotal role in ensuring regulatory approval across a diverse pipeline of assets. Senior Director Regulatory Affairs, Global Therapeutic Area Head. This role is an exciting opportunity to join as Senior Director Regulatory Affai...

Other organisations may call this role Graduate Toxicology Scientist, Junior Regulatory Scientist, Graduate Toxicologist, Graduate Scientist, Graduate Chemist, or Graduate Regulatory Scientist. Toxicology Regulatory Scientist. This is a unique opportunity for a talented science graduate with exce...

Regulatory experience in insurance (ICOBS), crypto-assets regulatory change (MICA), investment protections (MIFID), financial promotions, anti-bribery and corruption, conflicts of interest, conduct (Consumer Duty), and/or payments (PSR 2017). We’re looking for a Compliance Assurance Manager who’

A Regulatory Specialist with a chemistry background is urgently required to support the Global Product team for Regulatory Chemical standards by executing project tasks and/or assisting the Product Stewardship team. As a regulatory SDS and labelling specialist you would support the execution of d...

MERJE are pleased to be partnering with a leading Financial Services organisation who are seeking to recruit an experienced Prudential Regulatory professional to undertake the newly created role of Prudential Regulatory Liaison and Horizon Scanning Specialist. Develop and maintain relationships w...

As an experienced Regulatory Officer with solid SDS experience you will be involved and supporting all technical aspects of regulatory administration and support across the global business across Europe, Middle East and Africa region. Regulatory Officer £c60k Package. As regulatory officer you wi...

As the Regulatory Compliance Manager, you will be instrumental in ensuring our services meet all regulatory requirements and quality standards. Support the Nominated Individual and Registered Managers in all aspects of regulatory compliance, registration, and inspection processes. If you’re a pro...

Reporting directly to the Global Head of Regulatory, you will play a pivotal role in ensuring regulatory approval across a diverse pipeline of assets. This role is an exciting opportunity to join as Senior Director Regulatory Affairs, Therapeutic Area Head. You will lead a small team of Regulator...

Proven experience navigating MDR and FDA regulatory pathways. Regulatory Consultant – SaMD & AI Focus. You’ll guide clients through complex regulatory pathways and be exposed to a variety of responsibilities, typical projects could include;.

Our client, a continually expanding healthcare company is looking for a senior Regulatory director to join their team on an initial six-month assignment, to develop, lead and establish their regulatory strategy across lifecycle and new development assets. Acting as the primary liaison with regula...

Serve as a thought leader on regulatory affairs, defining European regulatory strategy and plan to maximize regulatory success. Serve as point of contact with EMA leading and managing regulatory interactions, building trusted relationships with regulatory authorities. Maintain currency of EU regu...

Fascinating opportunity for you as a German speaking Regulatory Manager to work across multiple EU markets. This global food business is looking for a Regulatory Manager to help them as they grow closer collaboration through their EU businesses. All they ask for is you have food regulatory experi...

Regulatory Affairs, regulatory compliance, study monitoring, study summaries, risk assessment, dossier writing, regulatory strategy, consortia support, consortia management, OR, advice/expertise, EU REACH, GB REACH, DUINS, grandfathering, industrial chemicals, biocides. We focus on recruitment in...

Partnering with an international pharmaceutical company focused on both in house product development and CDMO services, we are now supporting the appointment of a new Regulatory CMC Project Manager to oversee regulatory activities for a small molecule oncology product globally. Manage CMC regulat...

Utilize regulatory tools and databases to streamline operations and ensure regulatory deliverables are met. As we expand our footprint, we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services. Let's redefine regulatory exce...

Maintain meticulous documentation for regulatory filings and participate in internal and external audits. A strong background in regulatory affairs within the beauty, personal care, or related industries. Role: Regulatory and Technical Manager.

Preparing and compiling regulatory documentation, coordinating and executing regulatory submissions in compliance with ISO13485, IVD 2017/746 Regulation, FDA 21 Code of Federal Regulations (CFRs), Biologics License Applications (BLA), Medical Device Approvals (510(k)), Canadian Medical Device Reg...

You will be responsible for EU and ROW markets, managing the authoring and compilation of all necessary CTD and regional administrative documentation for CMC-related worldwide regulatory submissions, through direct liaison with globally located Regulatory and Technical Operations team members. Re...

To provide independent risk oversight and assurance of the Tier 1 and 2 risk and regulatory control environment through audits / assurance reviews and risk assessment for Concentrix and client regulatory and contractual requirements. Oversight to demonstrate compliance with Regulatory and Contrac...

A great opportunity which is being presented on a long term rolling contract basis (with no end date in sight) for a Regulatory Associate with a key manufacturing client in the area. Handling tasks to support regulatory processes and projects. Responsibility for tracking and co-ordinating registr...