Higher Scientist - Standards Lifecycle - £34,841 p.a. + benefits We are currently looking for a Higher Scientist to join our Standards Lifecycle team the Science, Research & Innovation group. This is a full-time opportunity, on
Job Description Qualified Person (QP)- Romford, Essex Competitive salary plus and benefits Permanent full time Ethypharm is a European-based specialty pharmaceutical company with global reach and is a committed player in the treatment of pain, addiction,
Job Description Regulatory Affairs Manager – 16-month FTC North London, UK – Hybrid £65,000 - £70,000 + Bonus Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines.
Job Description General Purpose of Role: To QP certify manufacturing processes/activities performed under PCI Pharma Services MHRA licenses. Main Responsibilities: To review Batch Manufacturing Documents to ensure compliance with UK and EU GMP and the Product Specification
Job Description There is a Quality Manager (RP) vacancy for a Pharmaceutical Company based in Hertfordshire! This is a permanent, on-site opportunity for an organization that imports and exports a wide range of healthcare products, domestically
Job Description Havas SO is a purpose-built healthcare communications agency bringing together a diverse team of creative and communication experts. What makes Havas SO different from others is that we can custom-build the best solutions for
Job Description Title: Principal Scientist – UK Based Location: Merthyr Tydfil, Onsite Contract Type: Permanent Company Summary Planet Pharma are partnered with one of our longest standing clients, seeking to hire a Principal Scientist to join
Job Description OBJECTIVE Maintaining the database through registration/transfer of patients, notifying consultants of abnormal results and answering telephone enquiries. To perform appropriate pharmacovigilance activities for company products ensuring that the company is compliant with relevant MHRA/EU regulations,
Job Description We are proud to tell you about Curia Curia is experiencing growth and we have an exciting opportunity for an experienced Program Manager to join our Glasgow site which is part of Curia Global.
The Quality Technician will assist the QA officer in the review of procedures, completed batch paperwork including manufacturing and analytical documentation. Be the QA representative for new campaigns dealing with aspects including process instruction sheets, change
Job Description OBJECTIVE To perform PV activities in line with relevant MHRA/EU regulations, directives and guidelines KEY ACCOUNTABILITIES Using the Global Safety Database, process safety reports received from all sources for assigned products, as per regulatory requirements
Assistant/Regulatory Affairs Manager Salary: £55k-65k Location: Watford Flexibility: Hybrid (3 days in office per week) Contract type: Permanent Job description Job description • Manage required regulatory processes for EU and UK products including national phase of
Hobson Prior are currently looking for a Quality Assurance Manager to join a brilliant pharmaceutical organisation on a permanent basis. Our client is focused on providing healthcare products for people who are severely ill.Please note that
Job Description AssureBio has exclusively partnered with a pharmaceutical business to recruit a new Head of Site Quality. This is a unique role that will require an individual to lead the way in assuring high quality
Job Description Job Title: Regulatory Affairs Manager Company: TORTUS AI Location: Holborn, London, UK About TORTUS AI: TORTUS is one of the fastest growing AI startups in the UK, building the next generation of AI co-pilots
Job Description QP Morpeth, Northumberland Up to £110,000 per annum + bonus + package Permanent role *Relocation Package if required* Cpl Life Sciences are partnering with a large pharmaceutical company in the North East of England,
Job Description DURATION – Starting as a 6 month contract SALARY- COMPETITIVE LOCATION- Heathrow area SUMMARY: This is the perfect time to join an exciting research-driven, biopharmaceutical company who work on reproductive medicine, gastroenterology and urology.
Job Description About this Opportunity: Our client, a Global Pharmaceutical CDMO, is seeking a Qualified Person to join their expanding Pharmaceutical manfacturing operation and become a key part of their leadership team. As the Qualified Person
Job Description The Company Fresenius Kabi is a global healthcare company that specialises in lifesaving medicines and technologies for infusion, transfusion and clinical nutrition. Our products and services are used worldwide to help care for critically
Job Description Title: Regulatory Submissions - Post Marketed Products - Global Company Company: Pharmaceutical Company Location: Slough About the Company: The company is a leading global pharmaceutical company dedicated to improving patients lives by developing innovative