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As a key member of the Operations Team, you will be responsible for the day to day management of plant operations, ensuring optimum levels of performance are achieved and sustained in accordance with license obligations and health and safety procedures. You’ll be an experienced manager, with ...

Providing innovative drug development plans, data gap analyses and international regulatory strategies for complex products within the changing regulatory environment. Representing clients in regulatory agency interactions and providing regulatory solutions to agency objections. Direct experience...

You will be expected to keep up to date with changing regulatory policy and proposed changes to legislation via membership of a relevant professional body or other equivalent means. Senior Agriculture Regulatory Approaches Advisor. This is an exciting opportunity to join NRW s Land Regulatory App...

A solid understanding of drug development and regulatory documentation requirements. We specialize in regulatory writing and consultancy services, providing best-in-class support to the pharmaceutical industry. Regulatory responses to health authorities.

RBB) to enable consistent and appropriate understanding and application by staff that enables effective regulatory service provision. Experience of understanding and applying regulatory activities. You will be expected to keep up to date with changing regulatory policy and proposed changes to leg...

Are you a hands-on Regulatory Affairs professional with a passion for clinical trials and a drive to grow into leadership? Join a dynamic, fast-paced SME-sized CRO specialising in oncology, where your expertise will shape the future of our expanding Regulatory Affairs team. Senior Clinical Regula...

Regulatory Solicitor / Associate / Legal Director - Safety, Health & Environment (SHE). Sector: Regulatory Defence (Health & Safety, Environment, Fire, Food, Product Safety, Inquests). We're working on behalf of a top-tier international law firm with a standout regulatory team, looking to welcome...

Regulatory responses and briefing documents. Develop and deliver high-quality regulatory documents in line with guidelines. Prior regulatory writing experience in the pharmaceutical industry, medical communications agency or CRO.

Job Title: Lead Factory Trainer (Maternity Cover- 12 months)Department: Group People and DevelopmentReports To: Factory Training ManagerLocation: Site BasedShift Pattern: Monday to Friday 12:00pm to 09:00pm (Tuesday and Wednesday) 8:00am to 5:00pm (Monday, Thursday and Friday)Pay Rate: Competitiv...

Demonstrated success in regulatory strategy development, multi-project leadership, and managing high-level regulatory authority interactions. Manage external regulatory service providers to align with business objectives and support the development and maintenance of an effective regulatory affai...

Lead Regulatory Approaches Advisor. Be the principal point of contact with environmental regulators, both UK and European, to share information and work together on the regulatory approach, technical advice and guidance for all relevant Sectors. Support the development and training of staff acros...

At Complete Regulatory,, we provide class-leading writing support and consultancy services to the pharmaceutical industry, producing a wide range of high-quality clinical documentation, including clinical study reports, protocols, clinical summaries, clinical overviews, regulatory responses and o...

RBB) to enable consistent and appropriate understanding and application by staff that enables effective regulatory service provision. Experience of understanding and applying regulatory activities. You will be expected to keep up to date with changing regulatory policy and proposed changes to leg...

Quality Assurance and Regulatory Affairs Consultant. Professional growth and development: You’ll have the opportunity to work on a diverse range of projects, from writing and editing regulatory documents to providing oversight for outsourced deliverables to our clients. Our services include devic...

Regulatory Strategy Development: Lead the development of regulatory strategies for CTAs in alignment with EU regulatory requirements. As we expand our footprint to Warsaw, Poland, we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulat...

We are looking to recruit Senior Regulatory Writers with at least 3 years' experience as a regulatory writer within the pharmaceutical industry and/or a medical writing agency. This position will benefit anyone looking to build on their experience in regulatory writing, while working within a hig...

Our work spans a wide range of high-quality clinical and regulatory documents, including:. Prior regulatory writing experience in a medical communications company, CRO or Pharma. You’ll play a key role in interpreting and communicating complex scientific data clearly and accurately for regulatory...

Scendea is an international product development and regulatory consulting group delivering market-leading scientific expertise & regulatory solutions, to advance healthcare innovation worldwide. Providing innovative drug development plans, data gap analyses and international regulatory strategies...

Senior Manager, Regulatory Medical Writing. The individual provides leadership with respect to all program documents and may act as the departmental expert on IND/IMPD dossier components, briefing documents, and responses to regulatory authorities across programs. The individual reviews documents...

Top ranked in Chambers UK and Legal 500; our Regulatory team are recognised as one of the best in the UK with a broad spectrum of knowledge and expertise. In this role, you will independently manage a litigation caseload, supporting the Regulatory team in delivering high-quality services to profe...

At Complete Regulatory, we offer. We specialise in delivering high-quality clinical and regulatory documentation across a wide range of therapy areas, including:. Develop and deliver high-quality regulatory documents in line with guidelines.

Are you a hands-on Regulatory Affairs professional with a passion for clinical trials and a drive to grow into leadership? Join a dynamic, fast-paced SME-sized CRO specialising in oncology, where your expertise will shape the future of our expanding Regulatory Affairs team. Regulatory Affairs wit...

The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases.

Lead regulatory interactions with authorities such as the FDA, EMA, and national agencies, while overseeing the preparation and submission of high-quality regulatory documents (e. Manage external regulatory service providers to align with business objectives and support the development and mainte...

The individual provides leadership with respect to all program documents and may act as the departmental expert on IND/IMPD dossier components, briefing documents, and responses to regulatory authorities across programs. The individual reviews documents within a therapeutic area with respect to c...

Do you have management experience, a consultancy background, and want to evolve in a leading Regulatory function?. This is a rare chance to shape regulatory programs at a global scale while staying deeply engaged with technical and strategic challenges. Guide clients through complex regulatory la...