Regulatory affairs jobs in Northampton

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 ...

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 ...

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 ...

Bachelor of Science degree in food science, chemistry or related field or equivalent qualification. * 2-3 years' experience in regulatory affairs within the food industry. * Strong communication ...

You'll get to learn about evolving regulatory requirements and you will be able to confidently support the Regulatory Affairs & Homologation Specialist with the ongoing administration that surrounds ...

Regulatory Affairs : Address regulatory issues promptly and thoroughly, ensuring compliance with all relevant regulations. General Requirements: * Excellent communication skills, both verbal and ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Administer regulatory affairs and conduct full investigations of incidents within strict timeframes. Qualifications and Experience: * Bachelor's degree in Biomedical Science or similar field

... affairs content. * You'll be part of ensuring stories from our region are heard on our national ... You'll have sound legal judgement and be proficient in Ofcom's broadcast regulations and guidelines

We are currently partnered with a global Pharmaceutical company who are now looking for a regulatory affairs associate to execute the Regulatory Plan/objectives to ensure the success of new product registrations for an initial 12-month-long contract with the likelihood of an extension. We have ex...

As the Head of Regulatory Affairs for the United Kingdom and Ireland, you will be responsible for leading and managing all regulatory activities to ensure compliance with applicable laws, regulations, and guidelines governing our organization's products and operations within these regions. This r...

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 ...

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...

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...

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...

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 ...

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...

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. ...

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 ...

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 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 ...

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...

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...

A long term Medical Device client of ours based in West Yorkshire, are looking to add a Regulatory Specialist to their team to support their growing business. They are looking for an individual that is hard working and self-motivated to assist with all things regulatory. When required, compile an...