Premier Work Support are excited to be recruiting for a Regulatory Affairs Product Manager for a ... US FDA medical device products including maintenance of regulatory registrations and listings ...
Ensure system compliance and quality assurance, collaborating with QA and Regulatory Affairs to meet global medical regulations and standards. * Design for Manufacture (DFM): Implement DFM principles ...
... affairs. The firm's services encompass pensions, investments, tax planning, cash flow modelling ... private medical insurance, and 25 days of holiday (plus bank holidays). If you are a driven ...
... g. medical, policy and public affairs, health and value, communications, legal, compliance, quality, regulatory, commercial and supply, working with the Glocal commercial teams to maximise UK ...
Associate Director, Medical Affairs. If you're a strategic innovator within Medical Affairs, this is an opportunity for you. ...
Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading global drug development organization. We are seeking a motivated individual with substantial experience in Medical Device Regulation, particularly in the areas of combination pr...
Great mix of global and EU med affairs and commercial work, across an established and growing osteoporosis account. ...
Medical Affairs Manager - Code Signatory & Business Partner. To ensure relevant UK Medical Affairs teams are kept abreast of global initiatives in market. Significant pharmaceutical industry experience in medical affairs as a Code signatory. BU working on BU related activities, such as corporate ...
Regulatory Affairs Officer, Compliance Officer, Pharmaceutical, COR5800. A Regulatory Affairs Officer / Compliance Officer is urgently needed to join a thriving scientific technology company in Lincolnshire. Regulatory Affairs Officer, Compliance Officer, Pharmaceutical. It’s a great opportunity ...
Regulatory Affairs Associate for a Global Healthcare Company who have opened a new vacancy within their Regulatory team on an initial 6-month basis based out of their offices in Tadworth. Maintain regulatory procedures to ensure consistent, efficient and compliant regulatory processes. The role e...
Regulatory Affairs Product Manager. PPE regulatory requirements and develop regulatory strategies and assessments to ensure successful achievement of business objectives. Follow company Regulatory Intelligence process to monitor the development of regulatory changes and communicate potential busi...
We are looking for an experienced Medical Secretary to join our healthcare team in Guildford. The successful candidate will have a strong background in medical administration, excellent organisational skills, and a commitment to providing high-quality support to our medical professionals and pat...
Maintain regulatory procedures to ensure consistent, efficient and compliant regulatory processes. Participate in project teams to define country regulatory requirements. Prepare accurate regulatory submissions to secure timely approvals in support of business initiatives. Support training on loc...
Senior Regulatory Affairs Specialist. Senior Regulatory Affairs Specialist opportunity working for a growing pharmaceutical company that specializing in medicinal, non-medicinal, medical devices, and OTC products. Due to the size of the business, a well versed Regulatory Affairs professional is r...
Regulatory Affairs Associate Manager - Cosmetics. Planet Pharma are partnered with a niche mid-sized CRO assisting them with the search for an Associate Manager, Regulatory Affairs to work on an initial 6+ month project with a focus on Cosmetic products. The Associate Manager will ensure products...
Medical Science Liaison – Nephrology / Rare Diseases. Providing medical information and responses to complex medical questions from clinicians. Working as part of a wider team, but with sole responsibility for specialist centres across UK, Netherlands and Ireland from a medical affairs standpoint...
Join a dynamic and ambitious truly independent agency as a Senior Medical Writer and immerse yourself in diverse, exciting meded, med affairs and omnichannel projects. ...
You're an established Senior Medical Writer, with either Medical Affairs or Publications experience, looking for the next challenge, or an experienced Medical Writer aiming to move up. Senior Medical Writers define new directions with CMC Affinity. IPG Health Medical Communications is home to the...
Expertise in authoring and reviewing of regulatory documents; development regulatory documents; Regulatory Strategy Plans, Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Orphan Drug and Paediatric plans/applicati...
Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to suppo...
VP, Medical Director, CMC Affinity - UK. We are CMC Affinity, and we are hiring for an VP, Medical Director to join our global team, based in the UK. IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, united by a healthy obsession with creatin...
Time for a change? My client has immediate need for a Scientific Director to head up a thriving oncology account - this role is mostly publications with some medical affairs and MedEd in the mix too. ...
Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone regulatory project, with guidance from senior staff as appropriate. May write new regulatory SOPs and regulatory intelligence databanks, and/or propose r...
