TOPRA Jobs - Regulatory Affairs vacancies
TOPRA Jobs is a specialist job board for regulatory affairs roles in the UK and mainland Europe. It is regularly used by a wide variety of global and regional organisations, as well as government agencies and consultancies.
Our jobs cover roles in the human medicines, medical devices and veterinary sciences sectors. We advertise all types of roles within the sectors, from senior executive to entry level (including paid internships).
Our clients have included AstraZeneca, GlaxoSmithKline, GSK, Merck, Mylan, Parexel, Pfizer, RB, Roche and many more.
TOPRA Jobs is regularly updated, so whether you are looking for your first job, career progression or a change of role, you’re in the right place.
For more info about us: https://www.topra.org/
TOPRA is the professional membership organisation for individuals working in healthcare regulatory affairs. We work with our members internationally to enable and promote excellence across the healthcare regulatory profession.
- Provision of highly respected regulatory training for over 40 years
- World-leading postgraduate qualifications
for regulatory affairs - Unique competency accreditation programme for regulatory professionals
- Peer-to-peer networking and quality resources for members
- Define values and standards of good practice.
TOPRA's values are to be: |
Our members say we are: |
Trusted | Respected |
Open | Educational |
Progressive | Professional |
Responsive | |
Authoritative |
Latest jobs
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Regulatory Affairs Specialist
Regulatory Affairs Specialist At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and
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Global Regulatory Affairs CMC Manager (100%) in the Albumins Team
For our Global Regulatory Affairs department, we are currently looking for a : Global Regulatory Affairs CMC Manager (100%) in the Albumins Team Do
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Manager, Clinical Quality Compliance
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovat
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QC Compliance Specialist
The QC Compliance Specialist will be responsible for managing QC's Change Controls/CAPAs and Workflows. In this role a typical day might include, b...
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Senior Manager Regulatory Affairs SFL
Would you like to join and contribute to a successful and growing multi-national organization in the heart of Europe and one of the world’s leading...
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Specialist, Regulatory Compliance
Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and
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Director, Regulatory Compliance Quality Operations - EMEA - Homebased
Who we are: Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology
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Principal Regulatory Officer / UK; Pharma & Generic Products / Project Manage
Principal Regulatory Officer / UK; Pharma & Generic Products / Project Manage Excellent opportunity for a 'top-end' Senior Regulatory Officer/Associ
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Continuous Improvement Officer III
Job description: We are at the centre of the rapidly growing cell and gene therapy sector. We deliver life-changing therapies to patients, and so can
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Sr SSU & Reg Specialist (Contract & Feasibility)
Senior Site Start-Up & Regulatory Specialist - Feasibility, Contract and Budget Specialist This is a sponsor dedicated opportunity in Copenhagen, D...
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Regulatory Affairs Associate Consultant
Mexico Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a...