Summary Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra. Dechra are a growing, global specialist within the w...
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Summary Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra. Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and ...
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The Recruitment Co are recruiting for a Study Monitor (Clinical Operations) to join our clients expanding team. A world-leading manufacturer of high-quality technical products. Contract: Permanent Salary: 28,017pa Shifts: Full time The Role: Oversee ...
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Job Title: Specialist Biomedical Scientist- Haematology and Blood Transfusion Location: Essex Salary: 35,392 to 42,618 per annum Joining Bonus of 5,000 and 1,500 wellbeing allowance Job Type: Permanent, Full time We are seeking an enthusiastic and mo...
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Quality Systems Analyst Medical Devices Plymouth Permanent Contract Focus of the role Principally to manage and control quality system documentation and eQMS consisting of Standard Operating Procedures, drawings, work instructions, procedures, materi...
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Our client is an established medical technology manufacturer producing molecular diagnostics and point of care devices for the international market. Due to rapid expansion they have a position for a 12 month fixed-term contract with the Quality Engin...
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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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Quality Assurance Executive Permanent position Manchester Salary negotiable bonus Cpl Life Sciences are partnering with a large pharmaceutical company to recruit for a Quality Assurance Executive. The purpose of this job is to assist the Head of Regu...
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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...
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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...
Position: Clinical Data Administrator Location: Witney Working Days: Mon-Fri Pay Rate: 30,000 Main Purpose of Role The primary objective of this role is to deliver high-quality and efficient data management support to Clinical Affairs, the Science Su...
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Position: Office Administrator (Support Clinical and Science Support teams) Location: Witney Working Days: Mon-Fri Pay Rate: 26,000 Main Purpose of Role The primary objective of this role is to deliver high-quality and efficient data management suppo...
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Quality Assurance Manager - Good Clinical Practice Our client, based in Cheshire are recruiting for a contract GCP QA Manager to join them for a 6 month project. This is an exciting opportunity to join a dynamic company with a great culture. Role: Pr...
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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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A new instruction for a temporary Lab Technician with a key manufacturing client in the area. The role is within the Quality Team. Benefits, Salary, Hours of Work & Culture: Excellent rate of pay Super professional, friendly, laboratory team setting ...
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