Trabajos regulatory affairs associate en Edinburgh

SRG are working with a global name in the pharmaceutical industry to help them find a QA Compliance Officer. If you have QA and/or Compliance experience from a GMP environment then this could be a great next step for you. Support tracking of site compliance commitments and follow up actions. Liai...

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...

This internship programme will help you build a fantastic online medical portfolio. This internship provides you with all the opportunities to grow - both within your role as a writer/editor and, more generally, as someone navigating the vast plain of career development. I have joined Klarity Hea...

IT Project Manager – 2 Year Fixed Term Contract (highly likely to become permanent) - £35,000 - £45,000 – Remote - Candidates need to be located in the UK. Harvey Nash has been engaged by an organisation with a brilliant social purpose to recruit an IT Project Manager on an initial 2 year fixed t...

Project management– effective project management to ensure the objectives of the project are realised for all stakeholders and milestones are achieved by following agreed upon processes and, where necessary, optimising BI resources, processes and networks to deliver projects. Project Manager (PM)...

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

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. ...

Do you have a passion for publications? How about a Senior Medical Writer role with one of the most rewarding and supportive, independent MedComms agencies?. You will need to have at least 3 years' experience writing for a Medical Communications agency, including publications, and be based in the...

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 ...

The Divisional Chief Risk & Compliance Officer for Davies UK&I will be accountable for the delivery of an effective and efficient Risk & Compliance infrastructure and function across Davies UK&I Division, with the purpose of:. Delivering at Divisional level all objectives set by the Group Chief R...

Drug Product Senior Manager / Associate Director. The main task of the Drug Product, Senior Manager / Associate Director is to lead projects from the technical feasibility evaluation through commercial registration of the company drug product portfolio. ...

Our client, a successful Investment Management firm, are looking for an experienced Senior Compliance professional to join the team to lead, oversee and manage the day to day compliance and operational aspects of their investment management business unit and platform offering, ensuring issues and...

An opportunity for an Associate Director, experienced in Environmental Consultancy / EIA, has opened at a global multidisciplinary engineering team covering Civil, Structural, Geotechnical & Environmental disciplines. As Associate Director you will be involved in a wide range of projects througho...

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...

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...

Are you an experienced Senior Medical Writer who loves working on scientific publications, engaging with clients and going on site?. You will need to be based in the UK and have at least 3 years' experience within medical communications. PR #medcommsjobs #nextmedcommsjobs #medcommsrecruitment #me...

This will be a highly diverse role; typical duties include answering complex customer regulatory enquiries, researching/impact assessing emerging regulatory issues, regulatory support to NPD, product notifications, REACH registrations, managing external expert consultants and, sharing your regula...

As a Principal Medical Writer at Real Chemistry you will be working across several therapy areas to create a range of material, ensuring the language and content is appropriate for the target audience. Medical Writing role within an agency environment. ...

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 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...

Senior Regulatory Affairs Associate (Interim - 1 Year) - Remote. Are you a detail-oriented Senior Regulatory Affairs Associate with a comprehensive understanding of regulations surrounding supplements and nutrition claims?. ...

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 ...

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. ...