Offres regulatory affairs à Chester

Reporting to the Chief Regulatory Officer, this role will be responsible for all regulatory activities for medical device and combination products, including defining the device regulatory strategy and overseeing all device submissions across global markets. Device Regulatory Affairs, Senior Dire...

Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...

Provide high level strategic and operational regulatory direction and mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approvals in international markets, regulatory strategic development plans and risk ...

This is a key new hire within the Scientific and Regulatory Affairs team – you will provide regulatory support to the chemicals management and Government and Public Affairs team. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, R...

Regulatory affairs CMC Consultant. Ensure that the content of CMC work-packages and documentation are phase appropriate, meet regulatory expectations and enable approval of regulatory submissions. At least five years in a scientific/technical CMC development or CMC – regulatory affairs function. ...

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. Minimum of 3+ years of experience in regul...

With broad and comprehensive expertise within the Regulatory environment you will lead project work and partner with the business to solve complex regulatory issues that impact the department or wider business. Support external regulatory agency audits, providing regulatory input to minimize pote...

Senior Regulatory Affairs Specialist who will be responsible for planning, creating, and implementing solutions for regulatory registration and release of products for distribution into specific geographies. Senior Regulatory Affairs Specialist – Medical Devices & IVD’s. Minimum of 4 to 5 years p...

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...

Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Main...

Works with the Lead, Regulatory Affairs, and the Development Team, and with moderate/minimal supervision, with select project teams within subsidiary organizations to develop and oversee program-specific regulatory, clinical, and development strategies. Responsible, with direction from Lead, Regu...

May write new regulatory SOPs and regulatory intelligence databanks, and/or propose revisions and/or act as reviewer for regulatory SOPs, as assigned and appropriate. Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for ...

Provide regulatory affairs expertise to clients seeking regulatory strategic input to their development programmes. Senior/Executive Director of Regulatory Affairs. Solid understanding of Regulatory Life Cycle Management and eCTD format for regulatory filings. Applies senior regulatory affairs ex...

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...

Job DescriptionWe are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products w...

We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, ...

As Associate Director, Global Regulatory Affairs Strategy, you will be responsible for:. Understand the regulatory landscape, assess regulatory risks, and develop global filing strategies. Align global development plans with regulatory requirements by integrating regional regulatory strategy liai...