Regulatory affairs jobs in Uxbridge

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, develop...

Implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements and manage the development of the regional product label by collaborating with the Labeling Working Group. Participate in core re...

Due to recent success within one our Innovative Biotech Clients I am recruiting for a Regulatory Affairs manager at ICON - Working in a client-dedicated yet fully embedded role ICON’s Regulatory Strategy group, you will lead or contribute to the development and execution of the drug development s...

We are recruiting for a Regulatory Affairs Manager - EU. The role reports to Director of Regulatory Affairs and is based in our offices near High Wycombe managing a small team. This role is responsible for regulatory efforts for EU and UK products, particularly post-Brexit, where the Marketing Au...

MERJE are partnered with a leading trading business who are looking for a Regulatory Affairs Associate to join their fast-growing team. Conduct Horizon scanning keeping the business informed of the regulatory landscape. Take an active role in training for different business areas on regulatory ob...

Leading a team of regulatory professionals, the successful candidate will oversee all regulatory compliance and communication with the relevant agencies and customers, and build and maintain relationships with regulatory authorities and other stakeholders in the regulatory framework. Norman Broad...

Regulatory Affairs – Senior CMC Dossier Manager. CMC dossier and evaluates/ensures that final versions comply with regulatory requirements and fulfill regulatory agency expectations with limited guidance from the manager. CPL has partnered with a world-leading Biotech looking for an experienced R...

As a Senior Regulatory Affairs Associate, you will play a crucial role in ensuring regulatory compliance for our medical devices. You will collaborate closely with the Regulatory Affairs Manager and cross-functional teams to prepare and review regulatory submissions, manage design dossiers, and f...

As a Senior Regulatory Affairs Associate in Labelling, you will play a crucial role in ensuring regulatory compliance and accuracy in product labelling. Our client, a global pharmaceutical company, is currently looking for a Senior Regulatory Affairs Associate - Labelling to join their team in Ux...

Conducts regulatory impact assessment and provide appropriate regulatory strategy for these changes that requires regulatory actions. Working with internal concerned departments, prepares appendices attached to regulatory CMC documents to be submitted to regulatory authority and submits them. CMC...

As a Senior Regulatory Affairs Officer, you will be responsible for managing regulatory submissions in the UK and European markets including supporting over 150 product licenses. Senior Regulatory Affairs Officer. Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical ...

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 ...

You will support the European Head of Regulatory Affairs and Pharmacovigilance in specific projects related to Alvita, including assessing the launch in new territories or the development of new processes necessary to deliver compliance with European and local legislation. This role will need to ...

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 ...

Regulatory Affairs Specialist. Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing multiple brands. Regulatory review and approval of product labelli...

The successful candidate will play a key role in product development, regulatory compliance, marketing strategies, and customer support within the OTC pharmaceutical sector. Ensure compliance with regulatory requirements and standards governing the manufacturing, labelling, and marketing of OTC p...

Provide regulatory affairs expertise to clients seeking regulatory strategic input to their development programmes. Scrip has an excellent reputation for providing strategic regulatory support and for delivering regulatory documents and processes. Our team is growing, and we are searching for hig...

Regulatory Affairs Specialist - Lifecycle Maintenance. We are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle ...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to unlocking ...

Quality Assurance and Regulatory Affairs Assistant Full-time position, Monday to Friday, 37.5 hours per week Salary is negotiable depending on qualifications and experience Facility is situated in ...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary ...

Alexander Lloyd are pleased to be partnering with a reputable Insurer on the hiring of a Regulatory Affairs Manager for their London office on a hybrid working model (2 days per week in the office ...

As the Regulatory Affairs Manager you will be responsible for EU regulatory activities including lifecycle management, submissions to EU regulatory bodies, preparing for new MAAs and developing ...

!*Regulatory Affairs Manager - Remote/hybrid in Uxbridge - Global Biotech*! Location: Hybrid in Uxbridge (Can be homebased but will need to attend office when required) Length: 12 month contract ...