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...the context of our growing activities, we are looking for a Regulatory Affairs Specialist to join our teams in Spain.
You will integrate a team of... ...for pharmaceuticals (NCE, Biologicals and Biotech), Medical Devices, Combination products and Cosmetics
Strong computer...
Medical device
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...initiatives. We work across the medical, industrial, chemicals and... ...designers, and consumer insight specialists.
To support Sagentia... ...are recruiting a Human Factors Regulatory Consultant to join our world... ...with multidisciplinary medical device development teams in Sagentia...
Medical device
We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for... ...a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be... ...guidelines.
Knowledge and experience of medical device legislation in relation to clinical...
Medical device
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Senior Regulatory Associate
Job Type: Permanent
Job Title: Regulatory Affairs Officer/ Senior Officer
Attractive salary and package
An exciting opportunity to... ...(CFRs), Biologics License Applications (BLA), Medical Device Approvals (510(k)), Canadian Medical Device...
Medical device
Permanent employment
Worldwide
...products, with over 650 products covering medical devices, cosmetics and biocides, currently sold... ...relationships with critical suppliers' regulatory and supply teams to facilitate the successful... ...support the European Head of Regulatory Affairs and Pharmacovigilance in specific...
Medical device
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Flexible hours
2 days week
3 days week
Job Title: Senior Regulatory Affairs & PV Manager
Employment Type: Permanent position
Hybrid)
Remuneration: Competitive salary and... ...pharmaceutical company specialising in medicinal, non-medicinal, medical devices, and OTC products. The business is increasingly growing and...
Medical device
Permanent employment
Local area
Hybrid work
...organisation who are seeking a Director of International Quality and Regulatory Affairs on a full-time permanent basis. You will promote and adhere... ...and compliance with updated requirements including EU Medical Device Regulations.
Highly competitive salary and 20% annual...
Medical device
Permanent employment
Full time
Local area
Hybrid work
£45k - £53k per annum
...The Scotch Whisky Association Department
Industry Sustainability
Job Title
Regulatory Affairs Manager
Working hours
35 per week (flexible requests considered)
Reporting to
Deputy Director, Industry Sustainability Team
Salary
c. £45,000 – £53,000...
Suggested
Full time
Work at office
Hybrid work
Flexible hours
As the Head of Regulatory Affairs for the United Kingdom and Ireland, you will be responsible for leading and managing all regulatory activities... ...affairs within the pharmaceutical, biotechnology, or medical device industry, with a focus on the UK and Irish markets.
Demonstrated...
Medical device
£95k - £100k per annum
Reference Number: JO-(***) ***-****
Regulatory Strategic Lead
Rate: £95,000 - 100,000
Job... ...leader is developing innovative products in medical devices and diagnostics. This organization has... ...-depth background working in Regulatory Affairs on Medical Device/Diagnostic products...
Medical device
Permanent employment
Work at office
...maintained in a validated state in line with regulatory guidance. This role involves... ...technical writing skills.
Proclinical is a specialist employment agency and recruitment... ...within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Medical device
For contractors
...The opening position available is for a Regulatory CMC Manager who is solely focusing on... ...relevant experience.
Proclinical is a specialist employment agency and recruitment... ...pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Regulatory
#
Medical device
Contract work
Remote job
£50k per annum
...Software Regulatory Affairs Specialist(NHS/Medical Devices) - New - Training and Progression!
Salary: £50,000 + Bonus & Benefits
A leading software house in the healthcare space requires a Software based Regulatory Affairs Specialist(NHS/Medical Devices) to join its...
Medical device
Remote job
Job Title: Medical Information Specialist - German Speaking Location : Remote (based in UK)
Planet Pharma... ...to the Pharmaceutical, Medical Device and Biotechnology industries across the... ...really makes us unique in our field. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions...
Medical device
Permanent employment
For contractors
Work at office
Immediate start
Remote job
Rotating shift
...YJ, UK Req #233 04 April 2024
Corin is seeking a Senior Regulatory Affairs Specialist to be responsible for product registration and all... ...through experience and a positive track record.
Experience in medical device/orthopaedics regulatory affairs, ideally Class 3 is...
Medical device
Permanent employment
Contract work
Work at office
Worldwide
Hybrid work
2 days week
A pharmaceutical client is looking for CQV Engineer for an ongoing project, which involves the qualification of process equipment.
This is an initial 6-month minimum contract role with the view to extend.Perform field activities including: Compile data and prepare reports...
Medical device
Contract work
Temporary work
€50k - €70k per annum
...Group is excited to be working alongside a medical technology organisation in their search... ...experiences in start-up and medical technology / device industry would be preferred but not... ...Ensuring compliance with regulatory standards
Identifying and mitigating risks...
Medical device
Hybrid work
Flexible hours
...the framework of internal and external regulatory guidelines and procedures.
Implement... ...industry, preferably acquired in Regulatory Affairs or Quality Assurance departments.... ...prescription and OTC pharmaceutical, and medical devices products.
Management experience.
Ability...
Medical device
Side job
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Regulatory Affairs Project Manager (Cosmetic)
Assist in the development of regulatory strategies for global product distribution
• Keeping up to date with regulatory developments in major markets
• Development and maintenance of regulatory quality systems to support post...
Medical device
...entities:
Phase IV Clinical Trials
Strategic Consulting
Regulatory Affairs & Quality Management
Linguistic Validation
~ A separate... ...and to develop partnerships with biopharmaceutical and medical device company clients.
With its head office in Lyon, France and...
Medical device
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