Freelance Regulatory Specialist- 12 month contract Im partnering with a fastgrowing organisation operating at the intersection of regulatory affairs and technology. They are seeking a Regulatory Affairs professional who is interested in taking their expertise in a new, forwardlooking direction. If you come from Pharmaceuticals, Medical Devices, or Biotech and youre curious about working in a...
Are you a Regulatory Affairs Specialist professional with experience supporting regulated products across global markets? Were looking for a Regulatory Affairs Specialist to take ownership of product Technical Files and support regulatory activities across multiple international markets. Salary & Benefits £32,000 - £42,000 (dependent on experience) 1 day WFH per week 33 days holiday...
Job Description Your new companyOur client is an internationally recognised leader in pharmaceuticals, medical devices, consumer health and related products. They have a need for a contractor for their regulatory team and are seeking a Senior Regulatory Affairs Specialist to drive product approvals and ensure continued compliance across key markets.This is a fantastic opportunity to join a...
An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. Responsibilities: - Primarily responsible for post-approval and compliance activities with a support role for the pre-approval team - Have an excellent understanding of and be able to execute activities related to...
Blackfield Associates are proudly partnered with an international pharmaceutical client on an exclusive basis, who are looking to establish a new team for their emerging markets division. To lead this team, we’re looking to hire a Regulatory Director to ensure successful registration, lifecycle management and global expansion of the portfolio, while providing leadership to a small team and...
Job Title: Regulatory Affairs Officer Job Type: Full-time, permanent position Location: Outskirts of Edinburgh, Scotland, UK – 3x a week on site. (Relocation support can be offered for the right candidate, however you MUST have the full right to work in the UK) Remuneration: £35,000 to £40,000 + benefits An exciting opportunity to join an established and growing IVD manufacturer and...
About Freyr Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. We partner with leading pharmaceutical, biotechnology, and medical device companies, delivering end-to-end regulatory operations support and regulatory strategy with precision, speed, and global expertise. Role...
🔬 Join a Dynamic Regulatory Team in the Crop Protection Industry! The Client: For over thirty years, our client, an Irish-owned family firm, has been a trusted supplier of plant protection products. They are keen on making sure their customers have a good experience all round, building proper long-lasting relationships, and keeping them coming back for more through good old-fashioned loyalty....
Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa. Clinigen is growing rapidly and is positioned well for an exciting future of continued...
Regulatory Affairs Director Our client is a young exciting publicly listed clinical-stage company dedicated to transforming the lives of patients in its therapy areas. With its novel and proprietary drug products and current clinical development programs our client is aiming to provide improved treatments for patients with increased remission rates, faster onset of action, durable effects, and...
A leading medical device manufacturer based in South Wales is seeking a Regulatory Specialist to join its Regulatory Affairs team. This is an excellent opportunity to be part of a growing, multinational organisation with a diverse portfolio of medical devices marketed globally. As a Regulatory Specialist, you will play a key role in supporting global product registrations and maintaining...
We are hiring a Regulatory Affairs Manager to support regulatory activities across a diverse pharmaceutical portfolio, including both marketed and pre-approval supply pathways. This role suits experienced regulatory professionals or individuals ready to step up into broader responsibility. The RA Manager will be managing 2 direct reports. Key responsibilities - Lead regulatory activities ...
Senior Regulatory Affairs (RA) Officer – Edinburgh – Medical Devices SRG are delighted to be working with an internationally renowned medical device manufacturer. As part of continued growth this organisation are looking for a Senior Regulatory Affairs (RA) Officer to join their team in the greater Edinburgh area. The Role As Senior RA Officer you will work as part of a large, multinational...
Position: Regulatory Affairs Associate Location: Gloucester Job Type: Permanent / Onsite (Hybrid) Our client, a global leading manufacturing business based in Gloucester are on the hunt for a detailed and organised Regulatory Affairs Associate! Role and Responsibilities – Regulatory Affairs Associate In this role, your key responsibility is to maintain regulatory compliance, obligations to...
Freelance Regulatory Specialist- 12 month contract I’m partnering with a fast‑growing organisation operating at the intersection of regulatory affairs and technology. They are seeking a Regulatory Affairs professional who is interested in taking their expertise in a new, forward‑looking direction. If you come from Pharmaceuticals, Medical Devices, or Biotech and you’re curious about working in...
Shape the Future of Regulatory Excellence with Shionogi At Shionogi, we are dedicated to protecting the health and well-being of people worldwide. As a global pharmaceutical leader, we are driven by science, innovation, and a deep sense of responsibility to public health. Join us in our mission to deliver life-changing treatments by ensuring robust regulatory strategies and compliance across...
Regulatory Affairs Manager - Leading Global Biopharma | UKYour new company Our client, a leading global biopharmaceutical organisation, is dedicated to advancing science and improving patient lives. With people at the heart of every decision, they are committed to ensuring patients today and for generations to come receive the treatments they need.We are supporting them in the search for an...
Job Description Are you a Regulatory Affairs Specialist professional with experience supporting regulated products across global markets? Were looking for a Regulatory Affairs Specialist to take ownership of product Technical Files and support regulatory activities across multiple international markets. Salary & Benefits £32,000 - £42,000 (dependent on experience) 1 day WFH per week 33 days...
Responsibilities: - Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications. Manages increasingly complex submissions making decisions independently and with minimal referral to line manager. - Ensure...
An excellent opportunity has arisen for an experienced regulatory professional to join my client, an established Regulatory consultancy, on an initial 12 month contract basis - the contract can be on a 6 or 12 month basis, full time or part time and fully remote based! The ideal person will have full life cycle experience, from CTAs through to registrations. As well as offering exposure to a...