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Hybrid working 2x a week Scope: This is an excellent opportunity for an experienced Clincial Trial Regulatory Specialist to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended. This role has come a...
Go to similar: Clinical jobs in maidenhead
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory...
Go to similar: Specialist jobs in maidenhead
Would you like to work on an industry leading high-performance computing platform? An opportunity is now available for a HPC Software Engineer to provide computer science support, through development and deployment of software techniques and solution...
Go to similar: Engineer jobs in maidenhead
Long Term Work at Household Name. On site Parking, Great Team , Lovely working environment 14.25 per hour. As a Laboratory Technician, you will have a specific focus on supporting the Laboratory Supervisor in the following: Responsible for the mainte...
Go to similar: Technician jobs in maidenhead
Do you have experience working within a highly sterile environment? Our client, a pharmaceutical company based in Borehamwood are looking for several Production Technicians to join their team. As the Production Technician you will be able to demonstr...
Go to similar: Technician jobs in maidenhead
Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: 22-25 per hour PAYE (inside IR35) We are partnered with a leading Pharmaceutical organisation who are looking for a jun...
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Quality Assurance Officer - Compliance 12 month Contract Buckinghamshire – Marlow Area 17.67 Subject to experience We are currently recruiting for one of the largest global pharmaceutical companies, recruiting for a Quality Assurance Officer to suppo...
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Exciting opportunity for a Production Manager to join a fast growing Medical Diagnostics manufacturer. The incoming individual will be responsible for overseeing all aspects of production operations, procedures and the Quality Management System and s...
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Clinical Evaluator An exciting opportunity has arisen for a Clinical Evaluator to join our thriving UK Medical Manufacturing Company. Working as an integral part of the Clinical Evaluation Team, the successful candidate will take responsibility for t...
Global Regulatory Affairs - Due Diligence Manager / Senior Manager Your new company This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a ...
Go to similar: Manager jobs in maidenhead
Lead Field Service Engineer Annual Salary: Up to 45k Location: UK-wide (with a focus on UK and Ireland) Job Type: Full-time We are seeking a Lead Field Service Engineer for a UK leading specialist supplier of Radiation Monitoring systems. This role o...
Go to similar: Engineer jobs in maidenhead
Quality Assurance Officer- Batch Release - Global Pharmaceutical Company Contract: 12-Month Contract Location: Marlow, UK Salary: 32,000 p/a Working Pattern: Hybrid SRG are working with a Global Consumer Pharmaceutical company to help them find a Qua...
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Job Title: Regulatory Life Cycle Management Scientist Location: Reading UK (RG2 Postcode) Rate: 18.85Ph - 33.31Ph PAYE - Depending on Experience Employment Type: Contract (12 Months) Hours: 37.5 hours per week Reference: PG3033 J ob Description: The ...
Go to similar: Manager jobs in maidenhead
The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Re...
Go to similar: Manager jobs in maidenhead
Are you a Trial Master File expert looking for your next role? Then, Cencora Pharmalex is your career opportunity Cencora PharmaLex is looking for an experienced Senior Trial Master File Study Owner to work within our Professional Services team on a ...
Are you a Trial Master File expert looking for your next role? Then, Cencora Pharmalex is your career opportunity Cencora PharmaLex is looking for an experienced Trial Master File Study Owner to work within our Professional Services team on a full-ti...
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