Trabajos regulatory affairs en Egham

CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to ...

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in Uxbridge or Cambridge on a contract basis for 12 months. Company: Our client is ...

Regulatory Affairs Coordinator CTA/CTR (Consultant) Job Type: 12 Month Contract Location: Berkshire, UK - 2 days on site per week Rate: Up to £55 per hour PAYE (inside IR35) We are partnered with a ...

Associate Regulatory Affairs Type: Contract Length: 12 Months Location: London We've currently partnered with a global pharma who are looking for a Associate regulatory affairs CMC in their London ...

Regulatory Affairs Associate Location: Maidenhead / M4 corridor. Salary: Very competitive salary on offer Planet Pharma are supporting a leading large global pharma company with the search for a new ...

Ensure system compliance and quality assurance, collaborating with QA and Regulatory Affairs to meet global medical regulations and standards. * Design for Manufacture (DFM): Implement DFM principles ...

We are looking for an Administration Officer to work in a busy, frontline position within Applications Management, Regulatory Affairs. Your role will be responsible for the overseeing of application ...

Work closely with legal and regulatory affairs to mitigate risks. * Reporting and Analysis: * Generate and analyse operational reports to track key performance indicators. (Delivery /transit times ...

Work closely with legal and regulatory affairs to mitigate risks. * Reporting and Analysis: * Generate and analyse operational reports to track key performance indicators. (Delivery /transit times ...

Serve as a local Medical Affairs representative in standing and project-based cross-functional ... regulatory or legal requirements * Provide brand support for the preparation and final signatory ...

Experience of working in medical affairs in the pharmaceutical industry * Therapeutic area ... Stakeholder management (specifically clinical, medical, legal/regulatory stakeholders internally ...

Manage and oversee the personal tax affairs for a diverse portfolio of clients, ensuring compliance with tax regulations and deadlines. * Provide expert advice on personal tax planning, minimizing ...

Job Description We have a fantastic opportunity for Global Product Regulatory Compliance Specialist reporting to the Product Regulatory Compliance Program Manager. As a Global PRC Specialist you will ...

... medical affairs in the pharmaceutical industry Therapeutic area experience of neurological ... legal/regulatory stakeholders internally, and external physicians) Apply: It is essential that ...

CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Regulatory Affairs Associate Role:. Experience in a Regulatory Affairs role in CMC, including preparation of submissions to Agencies and fami...

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...

Extensive experience in Regulatory Affairs with experience acting as therapeutic area European Regulatory Affairs lead, defining and implement regulatory strategies and executional plans. Define and advise the GRT on regional considerations in developing creative regulatory strategy, lead develop...

Working with the regulatory team (and core stakeholders across multiple areas), your role will be to operate as a Regulatory Lead, providing centralised regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved. A global pharmaceutical c...

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...

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 ...

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. ...

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 ...

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...

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...