Regulatory Affairs Jobs in Berkshire
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Search results - Regulatory Affairs Jobs in Berkshire
Randstad Delivery (GBS)-Maidenhead
as a Regulatory Affairs Specialist. You would be supporting across global patches with tasks ranging from international registration of products to impact assessments.
Role details:
Title: Regulatory Affairs Specialist
Start Date: ASAP
Pay rate: £121,000 per...
Verbatim Pharma-Slough
Job Description
Senior Regulatory Affairs Manager - Global Clinical Trial Services - Hybrid Opportunity
Are you ready to advance your career and join a business who are a leader in Clinical Services? Providing the opportunity to specialise...
Verbatim Pharma-Slough
Senior Regulatory Affairs Manager - Global Clinical Trial Services - Hybrid Opportunity
Are you ready to advance your career and join a business who are a leader in Clinical Services? Providing the opportunity to specialise in a niche area...
i-Pharm Consulting-Reading
Job Description
Job Title: Project Manager – Medical Affairs Communications
Location: Reading, UK
Contract: 6 months
Pay Rate: £35 - £40/hour
Hours: Monday – Friday, 37.5 hours per week
Our client is looking for a dynamic and organised Project...
Kao (UK) Ltd-Slough
Today, Molton Brown is one of the leading global brands in Kao's global cosmetics portfolio. Growing from small-scale artisans into the international fragrance brand it is today, its pioneering presence is felt in our stores and websites, travel...
CK Group-Reading
CK Group are recruiting for a Medical Affairs Project Manager, to join a leading provider of advanced analytics, research and technology solutions to the life sciences industry, at their site based in Reading, on a contract basis for 6 months.
Rate...
appcast.io -
Kao (UK) Ltd-Slough
Today, Molton Brown is one of the leading global brands in Kao's global cosmetics portfolio. Growing from small-scale artisans into the international fragrance brand it is today, its pioneering presence is felt in our stores and websites, travel...
Regulatory Affairs – Related jobs in Berkshire:
Reading
CK Group are recruiting for a Medical Affairs Project Manager, to join a leading provider of advanced analytics, research and technology solutions to the life sciences industry, at their site based in Reading, on a contract basis for 6 months...
cv-library.co.uk -
Randstad-Maidenhead
Affairs Specialist. You would be supporting across global patches with tasks ranging from international registration of products to impact assessments. Role details:Title: Regulatory Affairs SpecialistStart Date:...
randstad.com -
CK GROUP-Reading
CK Group are recruiting for a Medical Affairs Project Manager, to join a leading provider of advanced analytics, research and technology solutions to the life sciences industry, at their site based in Reading, on a contract basis for 6 months...
joblookup.com -
Karo Healthcare-Maidenhead
ownership, we're rapidly heading towards a €1 billion European leadership position in consumer health.
Join us at Karo Healthcare on our exciting journey. We're currently looking for a Team Lead Pharma Submissions & Compliance, Global Regulatory Affairs...
workable.com -
CK Group- Science, Clinical and Technical-Reading
Job Description
CK Group are recruiting for a Medical Affairs Project Manager, to join a leading provider of advanced analytics, research and technology solutions to the life sciences industry, at their site based in Reading, on a contract basis...
Planet Pharma-Reading
and regulatory affairs to drive product growth and ensure alignment with market needs.
Responsibilities:
• Product Strategy Development: Develop and execute comprehensive marketing strategies for allergy-related products, including new product launches, market...
Parkside Recruitment-Windsor
and guidance documents, e.g., in the area of Computerised System Validation, Data Integrity, Manufacturing, Pharmacovigilance, Clinical Development, Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance
• Experience as a Lead Auditor...
Planet Pharma-Maidenhead
to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities...
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