Regulatory Affairs Jobs in Reading
1 - 15 of 47
Search results - Regulatory Affairs Jobs in Reading
Pharma Partners Recruitment Ltd-Reading
Job Description
Job title: Pharmaceutical Affairs Officer (UK/IE)
A Pharmaceutical company in Berkshire are seeking a Regulatory Affairs Officer to join their team. This role will be responsible for the preparation, submission and follow up...
Freyr Solutions-Reading
About Freyr
Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. We partner with leading pharmaceutical, biotechnology, and medical device...
PE Global-Reading
Job Description
PE Global are currently recruiting for a Senior Regulatory Affairs Specialist with experience in Cosmetics and/or Medical Devices for a 5 month contract role with a leading multinational Consumer Health client based in Reading...
Reading
Pharmaceuticals Regulatory Affairs Associate – Homebased and Office
Opportunity:
This is a great opportunity for a Regulatory Affairs (RA) Specialist to develop your career in regulatory affairs for drug products.
Do you have experience in product...
cv-library.co.uk -
Freyr Solutions-Reading
About Freyr
Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. We partner with leading pharmaceutical, biotechnology, and medical device...
The RFT Group-Reading
Regulatory Affairs Director
Our client is a young exciting publicly listed clinical-stage company dedicated to transforming the lives of patients in its therapy areas. With its novel and proprietary drug products and current clinical development...
Reading
Talentmark is recruiting for a Regulatory Affairs Specialist to join a company in the Pharmaceutical industry, at their site based in Reading, on a contract basis initially for 6 months.
Salary: £63.52 per hour PAYE or £86.22 per hour Umbrella...
cv-library.co.uk -
Regulatory Affairs – Related jobs in Reading:
Pharma Partners Recruitment Ltd-Reading
Job title: Pharmaceutical Affairs Officer (UK/IE)
A Pharmaceutical company in Berkshire are seeking a Regulatory Affairs Officer to join their team. This role will be responsible for the preparation, submission and follow up of registration...
Reading
TalentMark is recruiting for a Regulatory Affairs Specialist to join a company in the Pharmaceutical industry, at their site based in Reading, on a contract basis initially for 4 to 6 months.
Salary: £50.75 per hour PAYE or £68.89 per hour...
cv-library.co.uk -
GS1-Reading
Position Overview
The Director, Healthcare Global Regulatory Affairs and Public Policy is a leadership role responsible for shaping and advancing GS1’s global healthcare regulatory and public policy agenda. The role operates at the intersection...
Fusion Group-Reading
need?
• Degree in life sciences, pharmacy or related field (advanced regulatory qualification desirable)
• Proven experience in regulatory affairs or regulatory intelligence within biotech, pharma or CRO environments
• Strong hands-on exposure to Early...
Planet Pharma-England
Regulatory Affairs Manager (EU) | Leading Pharma
We’re hiring a Regulatory Affairs Manager to support products in development and post-MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global...
SRG-Reading
analysis, and study design.
• Support short‑ to medium‑term strategic planning for global RWE programmes and Medical Affairs evidence generation.
• Contribute to submissions to regulatory agencies, NITAGs and health authorities, including key documents (e.g...
Uniphar Group-England
The role:
• The Director of Regulatory Affairs is responsible for assigned regulatory strategy and operations related to unlicensed medicines (ULMs), early access programs, and commercial product launches across Europe. This role ensures regulatory...
Planet Pharma-England
Regulatory Affairs Manager (EU) | Leading Pharma
We’re hiring a Regulatory Affairs Manager to support products in development and post-MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global...
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