Regulatory affairs jobs in Southall

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 ...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Associate to join their team in Uxbridge. Working in a busy global department, there is a focus on ...

Regulatory Affairs Officer (Hybrid working) I am currently working with a Parrell Import organisation based in North East London, this is a great opportunity for someone wanting to progress their ...

A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an ...

As Associate Director, Global Regulatory Affairs Strategy, you will be responsible for: * Lead the global regulatory strategy for biomarkers, companion diagnostic tests, digital health, and other ...

Responsibilities · Responsible for maintaining and supporting the promotion of regulatory affairs and ensuring that overall regulatory compliance of the Company, is maintained. · The position ...

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 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 ...

The Regulatory Affairs function understands, provides advice on and influences the various regulatory components of the energy sector so that ... ZIPC1_UKTJ

Reporting to the Senior Regulatory and Quality Affairs Manager, you will actively contribute to the development and maintenance of an effective Quality System, ensure compliance of the products to ...

Partnering with BT's wider Regulatory Affairs team in interactions with Ofcom in the UK, and colleagues in other jurisdictions. What you'll be doing * You will report to a Senior or Principal Lawyer ...

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 ...

Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France ...

The role will be supported by the; · Product team - constantly improving software to meet the delivery team's needs · Regulatory affairs team - understanding client business and compliance ...

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 ...

... affairs and avoid abuse of the privileged relationship that exists caring for vulnerable adults. * To adhere to all regulatory and statutory obligations and Tezlom's policies, procedures and ...

Joining the Agile Talent Community as an Interim Regulatory Reporting Consultant, you will have the freedom to work on projects that you choose, whether full or part-time within FS BRS and support ...

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 ...

Provide QA support during regulatory authority inspections, as applicable. * Carry out internal and external audits. RA Responsibilities * Maintain effective control of the license portfolio ...

Contribute to strategic improvement projects to improve business processes in line with the applicable regulatory requirements and Medicareplus Regulatory Strategy * Prepare and present Quality Data ...

Liaise with clients and suppliers to address quality issues and discrepancies. * Assist in the preparation for annual audits and regulatory inspections. Requirements: Experience: * Essential