Regulatory affairs associate jobs in Leicester

Senior Regulatory Affairs Officer (Maternity Cover). Senior Regulatory Affairs Officer opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-orient...

Associate Director (Regulatory Affairs). As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory Affairs. Title: Associate Director (Regulatory Affairs). Lead an...

Based in the UK, the Regulatory Affairs Associate is expected to;. Keeping up to date with regulatory and legal changes in EU. Preparing pre- and post-authorisation regulatory documentation and applications. Providing general regulatory advice to company's staff. ...

Looking for a Senior Project Manager to join a superb Azure partner to lead their PM function. Multiple projects – 4-8 projects. Want multiple, complex, challenging projects in which you can make a real impact?. You will be managing medium to large projects as well as assisting the Junior PM with...

BioTalent are working with a Global Consultancy business in their search for an Associate Director Regulatory Labelling for a 12 month contract. ...

Bioconjugation projects are carried out in Germany, Enzyme projects are based in Austria and biological IVD reagents in Ireland. To manage and deliver Complex Chemicals projects globally and with external partners, within budget, to agreed quality standards and other stipulated criteria. To manag...

We are seeking a highly motivated and experienced OTC Pharmaceuticals Specialist to join our team. 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 r...

They will also effectively manage, monitor and present project updates to relevant stakeholders, clients, or project team members. The ideal candidate will already work in commercial construction in the UK and be responsible for planning, coordinating, and implementing projects within the decided...

Senior Regulatory Affairs & PV Manager. Senior Regulatory Affairs & PV Manager opportunity working for a growing pharmaceutical company specialising in medicinal, non-medicinal, medical devices, and OTC products. Ensuring that regulatory processes are completed and products are launched in line w...

We are looking for an assistant project manager looking to develop their career within an organisation that is growing fast, working on a diverse caseload and providing excellent client service. We believe in providing our client managers with the bandwidth they need to be consultative and proact...

RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. Working knowledge and experience within an IVD Regulatory Affairs function. Experience wi...

We're looking for a Project Manager who will deliver bespoke engineering solutions to customers on time, on budget and to specification whilst following internal company processes for project delivery, complying with required standards and observing customer specific documentation and communicati...

Regulatory Affairs Manager (Parallel Import). Regulatory Affairs Manager opportunity working for a family-run pharmaceutical company that specialise in generic, OTC, medical devices, and prescription medicines. Seeking a detail-oriented Regulatory Affairs Manager with experience in Parallel Impor...

Control Now (CN) is looking for a Regulatory Affairs Manager to support the business with monitoring and interpreting regulatory change and notifications. The Regulatory Affairs Manager will play a vital role in supporting the product, marketing and management teams to stay informed with changes ...

A Project Manager to play a critical role in overseeing and managing the construction project within the facility. Regularly assess project risks and implement appropriate measures to ensure project success and safety. Lead and motivate project teams to achieve project objectives while fostering ...

Senior Regulatory Affairs Specialist - Medical Device. Perform Regulatory tasks to ensure compliance with regulations. Prepare regulatory documentation and submissions for product approvals. Develop regulatory plans/strategies for new products and changes to existing products. ...

Lutine Bell are supporting a leading Financial Services firm in the Midlands to appoint a Prudential Compliance Officer. The ideal candidate will possess a comprehensive understanding of regulatory frameworks and compliance requirements, coupled with the ability to interpret complex regulations e...

Recruitment of Associate and Full members, with support from the CEO and other team members * Sale ... To work with regulatory, sustainability and public affairs team on joint member visits (in line ...

As Regulatory Affairs manager, you will:. To be considered for the role of Regulatory Affairs Manager, you will have the following:. Minimum of 5 years of Regulatory Affairs experience in a relevant pharma company. Our client, a leading independent pharmaceutical company who have a wide range of ...

Based in the UK, the Regulatory Affairs Associate is expected to;. Keeping up to date with regulatory and legal changes in EU. Preparing pre- and post-authorisation regulatory documentation and applications. Providing general regulatory advice to company's staff. ...

Associate Director (Regulatory Affairs). As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory Affairs. Title: Associate Director (Regulatory Affairs). Lead an...

Senior Regulatory Affairs Officer (Maternity Cover). Senior Regulatory Affairs Officer opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-orient...

As Regulatory Affairs manager, you will:. To be considered for the role of Regulatory Affairs Manager, you will have the following:. Minimum of 5 years of Regulatory Affairs experience in a relevant pharma company. Our client, a leading independent pharmaceutical company who have a wide range of ...

Senior Regulatory Affairs Associate (Interim - 1 Year) - RemoteAre you a detail-oriented Senior Regulatory Affairs Associate with a comprehensive understanding of regulations surrounding supplements and nutrition claims?This 12-month interim role offers a high degree of autonomy and the flexibili...