Principal Regulatory Affairs Consultant

We are looking for a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global pharmaceutical environment.This is a client dedicated project,...

We are currently looking for Regulatory Affairs Professionals experienced in Clinical Trail Applications (CTAs) under EU-CTR directive. You can join us or our client dedicated projects and act as a Regulatory Affairs Consultant or Regulatory Affairs Senior Associate. This role can be based in either UK or UE (home/office based). In this role you will...

Description Principal Medical Writer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the...

Description Senior Medical Writer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center...

A rare opportunity for an aspiring regulatory affairs officer to join the regulatory team at a global chemical products business:Work under the supervision of an experienced regulatory managerProvide regulatory support to a wide range of chemical productsOngoing and comprehensive training. An excellent opportunity to start and establish your career in...

Do you want to use your extensive experience in Biodegradation in an exciting new role? Will you lead and deliver the best possible service to our clients and stakeholders? At our site in Alconbury near Huntingdon, Cambridgeshire we are looking to recruit the company's Principal Biodegradation Scientist within the Environmental Sciences team. Please...

Regulatory Affairs Manager (UK & Ireland)As the Regulatory Affairs Manager for the UK and Ireland, you will report directly to the UK Country Manager. You will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. Additionally, you will serve as the Local Person for Pharmacovigilance (LPPV)...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

Description Senior Medical Writer Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center...

Cure Talent is thrilled to partner with a leading Medical Devices Manufacturer, who due to continued growth, has an exciting opportunity for an experienced Regulatory Affairs Associate to join their team.As the new Regulatory Affairs Associate, you will be responsible for supporting global product registrations, maintaining design dossiers, and ensuring...

Cure Talent are delighted to be working with a well-established Medical Device company that supply and distribute innovative Medical Devices. Due to their continued growth and success, we have an exciting opportunity for a Senior Regulatory Affairs Associate to join them in West Yorkshire.As the new Senior Regulatory Affairs Associate, you will be working...

An opportunity to join the Chemical Regulatory science team at an R&D focussed global PPP company. We are looking for an aquatic ecotoxicology risk assessor; this is a junior/mid-level position working alongside very experienced regulatory ecotoxicology professionals.The role involves:Developing dataRisk assessmentsProducing the ecotoxicology section of...

An opportunity to join the Chemical Regulatory science team at an R&D focussed global PPP company. We are looking for an:Ecotoxicology regulatory specialist 2-5 years industry experienceIdeally with aquatic knowledge and some experience of risk assessment. The role involves developing data, risk assessments and producing the ecotoxicology section of...

Senior Quality Assurance and Regulatory Affairs ManagerPart-Time/Consultant Remote (Preference UK/EU Based)Our client is a licensed cannabis supplier of CBD/THC products to global pharmaceutical businesses, with business operations across multiple continents.They are seeking an experienced and dynamic Senior Quality Assurance and Regulatory Affairs Manager...

Northreach have partnered with an exciting pharma company based in the UK that are recruiting for a Global Head of Regulatory Affairs to join their team. . The role will lead the regulatory team, interfacing with regulatory agencies like the MHRA, EMA, FDA, preparing and submitting regulatory documents, and managing risk. The role requires a deep...

Blackfield are pleased to be partnered with an international business, with a requirement for a Senior Manager, European Regulatory Affairs, to ensures all regulatory and compliance activities across Europe are effectively managed, supporting the distribution, R&D, and marketing of products.This role leads the European Regulatory Affairs team, partners with...

ABOUT THE ROLE The Director, Global Regulatory Affairs will be responsible for developing, implementing, and advising on global regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives.DESCRIPTION OF THE ROLE• Provide high level strategic and operational regulatory direction and...

Unlock Your Potential in CMC Regulatory Affairs!Are you a seasoned expert in Chemistry, Manufacturing, and Controls (CMC) with a passion for driving high-quality regulatory submissions? We're looking for a dynamic leader to steer multi-modality projects from development to commercialisation.Key Responsibilities:Lead the preparation and submission of CMC...

Our client, a global pharmaceutical company is currently looking for a Senior Regulatory Affairs Portfolio Manager to join their team based on the outskirts of London on a full time, 8-month temporary basis (35 hours per week). This is a remote-by-design role which will require flexibility to attend key meetings on-site (Uxbridge). This opportunity will see...

Overall Job Purpose:The Regulatory Affairs (RA) Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of Sun Pharma’s pharmaceutical and medical products in order to control the safety and efficacy of these products. The RA Officer combines scientific, legal and business knowledge to ensure Sun Pharma’s...