Regulatory Affairs Specialist Jobs in Cumbria
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Search results - Regulatory Affairs Specialist Jobs in Cumbria
Cure Talent-Carlisle
Cure Talent is delighted to be working with a fast-growing specialist consultancy that delivers tailored Quality and Regulatory support to some of the UK’s most exciting MedTech innovators.
Make your application after reading the following skill...
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beBee Careers-England
Key Skills
• Project management and multitasking skills
• Strong communication skills
• Team player
• Solution focussed.
• Ability to build and maintain relationships
• Fluent knowledge of written and verbal English
• Highly organized and...
Cure Talent-Carlisle
Cure Talent is delighted to be working with a fast-growing specialist consultancy that delivers tailored Quality and Regulatory support to some of the UK’s most exciting MedTech innovators.
Scroll down the page to see all associated job...
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Planet Pharma-England
firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical...
Planet Pharma-Carlisle
expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications...
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GENinCode Predictive Genetics-England
regulations for In-Vitro Diagnostics Devices or Medical Device (software); in particular FDA 21CFR Part 820/Part 11, IVDR and ISO 13485.
• Minimum of 5 years of experience in regulatory affairs for in-Vitro Diagnostics Devices or Medical Device (software...
Planet Pharma-Carlisle
firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical...
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SRG-England
Job Description
Job Title: Medical Information Customer Experience Specialist (MICES)
Location: Tadworth – Hybrid (2-3 days onsite)
Employment Type: 12 months Contract – Strong likelihood of extension
Role Summary
We are looking for a Medical...
Indegene-Carlisle
regulatory guidelines, publication requirements, commercial and marketing requirements, etc. to develop quality medical content in broader content areas.
• Work with the medical information and medical affairs teams during congresses, product launches...
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Planet Pharma-England
Quality, Regulatory Affairs, R&D, and Program Management—to ensure legal documents align with business goals and timelines.
• Maintain and update contract templates and assist in improving contracting processes and tools.
• Coordinate with external legal...
Planet Pharma-England
bodies for our commitment 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...
Planet Pharma-England
commitment 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...
Planet Pharma-England
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...
Planet Pharma-England
bodies for our commitment 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...
Planet Pharma-England
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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