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

Scendea is an international product development and regulatory consulting group delivering market-leading scientific expertise & regulatory solutions, to advance healthcare innovation worldwide. Are you looking to advance your career in regulatory affairs?. If you are experienced in regulatory affai

Are you an experienced regulatory affairs professional with deep expertise in Chemistry, Manufacturing, and Controls (CMC)? We’re looking for a Senior Manager to join a dynamic Medicine Development team supporting multiple projects from development through post-approval stages. Proven track record

Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinical Trial Applications (CTAs) and Marketing Authorization Applications (MAAs). Proven experience in CMC re

Umbrella Regulatory Publishing Assistant Role: - Support publishing activities, ensuring accuracy and timely completion to challenging deadlines- Collaborate with team members to ensure successful delivery of the portfolio- Assist in the future delivery of innovative solutions, ensuring seamless i

Umbrella Regulatory Affairs Consultant Role: The Regulatory Affairs Consultant EMEA (Self Care) is responsible for the development of regulatory strategies across the EMEA region, and globally as relevant, providing regulatory input and technical guidance on regulatory requirements to product develo

Are you an experienced Regulatory Affairs Manager looking to make a impact in the chemical manufacturing industry? We are seeking a proactive and detail-oriented professional to lead the regulatory strategy and ensure full compliance across site operations. As a Regulatory Affairs Manager , you will

Umbrella Regulatory Publishing Assistant Role: - Support publishing activities, ensuring accuracy and timely completion to challenging deadlines - Collaborate with team members to ensure successful delivery of the portfolio - Assist in the future delivery of innovative solutions, ensuring seamless i

Umbrella Regulatory Publishing Assistant Role: - Support publishing activities, ensuring accuracy and timely completion to challenging deadlines - Collaborate with team members to ensure successful delivery of the portfolio - Assist in the future delivery of innovative solutions, ensuring seamless

The Principal Regulatory Affairs Specialist will provide expert level regulatory support and direction to products from concept to launch, and beyond into post market, as well as regulatory processes. Supports Regulatory Affairs Project core team members on development teams, providing regulatory gu

This position will contribute to the build-out of the regulatory affairs function at Edgewise and will provide regulatory expertise from preclinical through clinical development for our programs. Associate Director / Director, Regulatory Affairs (EU- or UK-based). Responsible for regulatory clinical

Graduation in pharmacy background or any relevant degree.Supervision and motivation of national approval team members.Contact person for all team members.Proactively ensuring smooth team operations and effective collaboration.Creating an inspiring team environment with an open communication culture.

Role: Principal Regulatory Specialist. A global company is seeking to expand its regulatory team and is looking for a talented individual to join. Experience evaluating manufacturing changes for impact on global regulatory submissions.

Lead and manage CMC-regulatory activities across various development and marketed products, ensuring compliance and regulatory risk mitigation. Are you an experienced regulatory affairs professional with deep expertise in Chemistry, Manufacturing, and Controls (CMC)? We’re looking for a Senior Man

Perform tasks associated with the Regulatory Affairs department at the highest level. Obelis Group is a quality driven, service-oriented company with over 30 years of experience in regulatory affairs. Regulatory Affairs Consultant - Cosmetics.

The Head of Product Compliance + Regulatory Affairs will lead and oversee HH Global's compliance framework to ensure adherence to evolving global legislations, regulations and industry standards. As the Head of Product Compliance + Regulatory Affairs, you will continue to build on the progress made

The Senior Manager, Regulatory Affairs will be a strategic thinker, responsible for researching and assessing regulatory precedence and contributing to regulatory strategies for development of Compass Pathways investigational drug programs. This position assists in maintaining organization’s Regul

The Senior Manager will interact closely with corresponding functional team members within the Company and will report directly to the Senior Director (EU Regulatory Lead), Regulatory Affairs. The Regulatory Affairs Senior Manager provides regional (EU and other ex-US countries) support for all regu

The Principal Regulatory Affairs Specialist will provide expert level regulatory support and direction to products from concept to launch, and beyond into post market, as well as regulatory processes. Supports Regulatory Affairs Project core team members on development teams, providing regulatory gu

Regulatory Affairs CMC Senior Manager. Change Control assessment experience (application of relevant regulatory guidance to proposed change). Support regulatory CMC writing activities including authoring CMC sections.

Work with the Global Regulatory Lead and Regulatory Affairs management to lead and define regulatory strategy and to compile and submit, in a timely manner, regulatory documents according to regulatory requirements and lead EU HA interactions. The Senior Manager of Regulatory Affairs Strategy, will

The Regional Regulatory Affairs Lead will provide sound regulatory advice, support the launch & re-launch of products in an efficient manner, ensuring all formulations and product claims meet legal requirements and align with company policies. BSc / MSc Degree in Food Legislation, Regulatory Affairs

We are looking to expand our Regulatory Affairs team and are currently looking for an experienced Regulatory Consultant to join us on a one-year fixed contract or a permanent basis. We are a forward-thinking regulatory affairs consultancy, DLRC Ltd takes the time to understand individual needs and f

This includes developing the vision for and responsible for overall leadership and strategic direction of the Regulatory Affairs team to ensure licenses are obtained in a timely manner in line with business strategy and the business markets products with consistently high quality, safety and efficac

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 regulatory services. Regulatory Affairs Manager Clinical Trials. Freyr is a fast-growing, innovative company specializing in providing end-to-en

Develop and execute CMC-regulatory strategies and oversee the preparation of key regulatory documents, including Module 3 sections. Proven track record in CMC-regulatory affairs within the pharmaceutical industry. Lead and manage CMC-regulatory activities across various development and marketed prod

The successful candidate will play a critical role in ensuring compliance with global regulatory requirements, leading technical file preparation, regulatory approvals, and new product submissions. Minimum of 3-5 years’ experience in regulatory affairs within the medical device industry. Sign in t

Provide ongoing regulatory support to the regulatory affairs team lead and project teams to ensure regulatory concerns are addressed and relevant data is generated to meet project objectives. Document and track regulatory submissions and regulatory authority license approvals for the EU market, part

The Director of Regulatory Affairs will lead the regulatory function and play a central role in shaping and executing global regulatory strategies for our ophthalmology assets. Regulatory Affairs, with significant exposure to ophthalmology or related therapeutic areas. Strong experience in authoring

Provide expertise as the Global Regulatory Lead to Product Development Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and outside. Provide expertise as the Global Regulatory Lead to Product Development Teams and regulatory single point-of-contact for produ

Quality Assurance and Regulatory Affairs Manager. Quality Assurance & Regulatory Affairs Manager. An opportunity has become available for an experienced Quality Assurance and Regulatory Affairs Manager to join the company on a permanent basis.

In the Regulatory Affairs team, you’ll support and strengthen Monzo’s regulatory relationships and work closely with Executives to help shape our vision and regulatory affairs strategy as Monzo continues to grow. For Regulatory Affairs this means ensuring our regulators are kept informed, managi

HC UK/I Regulatory Affairs Lead page is loaded. HC UK/I Regulatory Affairs Lead. Inputs into Home Care Global Regulatory Affairs (RA) strategy.

This role will provide strategic regulatory and scientific support on non-clinical and clinical development plans and work with both Regulatory Affairs - Strategic Project Leads and Regulatory Affairs - Life cycle management teams with an objective of getting fast access of innovative medicines to p

As an Senior Manager, Global Regulatory Affairs, Precision Medicine, you will help develop and execute Precision Medicine regulatory strategy in alignment with the drug global regulatory strategy and in compliance with the appropriate IVD regulations. Represent Regulatory Affairs Precision Medicine

Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinical Trial Applications (CTAs) and Marketing Authorization Applications (MAAs). Proven experience in CMC re

Maintain internal product documentation to ensure accuracy and regulatory alignment. Deliver training to internal teams on regulatory topics and updates. Minimum 5 years of experience in a regulatory or technical role within food, feed, chemicals, or related sectors.