36 Document Jobs

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Quality Associate

Quality Associate

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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Quality System Analyst

Quality System Analyst

21 May by Adecco

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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Laboratory Technician

Laboratory Technician

Scientific Laboratory Technician – Oxford. Are you looking to start your career within the Scientific industry or have current experience with Lab Maintenance to offer? Then look no further with this Scientific Laboratory Technician role. As a Scient...

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Regulatory Affairs Labelling Manager contract

Regulatory Affairs Labelling Manager contract

Regulatory Affairs Labelling Manager Your new company This consultancy is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Affairs Labelling professional for a contract job. This job is outside IR35 and ha...

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QA & RA Officer

QA & RA Officer

Evolve are recruiting for a leading medical technology organisation who are seeking a Quality Assurance and Regulatory Affairs Officer You will be responsible for providing technical support, guidance, and discipline for medical device manufacturing,...

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Field Service Engineer

Field Service Engineer

20 May by Reed

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...

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Study Manager Team Lead

Study Manager Team Lead

We have an exciting new opportunity for a Study Manager Team Lead to join a leading international CRO based in the North Yorkshire area. As the Study Manager Team Lead you will be responsible for directly line managing a team of Study Managers for re...

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Quality Engineer

Quality Engineer

20 May by Real Staffing

Are you a Quality Engineer with a passion for ensuring product quality and patient safety? We're seeking a Quality engineer to join a leading Global Medical Device Company, where you will play an important role in the execution of sound quality pract...

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QC Analyst - Level 1

QC Analyst - Level 1

23 April by SRG

QC Analyst - Global Pharmaceutical company Contract: 12 months contract Location: Worthing, UK SRG are working with a global pharmaceutical company to help them find a Lab Analyst to join their busy team. This is an exciting opportunity for an enthus...

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Regulatory Specialist

Regulatory Specialist

9 May by SRG

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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Quality Assurance Executive

Quality Assurance Executive

1 week ago by Cpl Life Sciences

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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Quality Assurance Officer

Quality Assurance Officer

15 May by The One Group

Cambridge is well-known for its cluster of Medical Device organisations but this one really is genuinely one of the special ones. With their ethos at the heart of what they do, they are passionately working towards saving thousands of lives through e...

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Senior Trial Master File Study Owner

Senior Trial Master File Study Owner

8 May by Pharmalex

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 ...

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Trial Master File Study Owner

Trial Master File Study Owner

8 May by Pharmalex

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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Regulatory Coordinator

Regulatory Coordinator

30 April by Cpl Life Sciences

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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Office Administrator

Office Administrator

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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