Medical Affairs Jobs in Tyne and Wear
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Search results - Medical Affairs Jobs in Tyne and Wear
Entrust Resource Solutions-Newcastle upon Tyne
Senior Regulatory Affairs Associate
Medical Device
West Lothian ~ remote working available but hybrid preferred
After an incredible 12 months of working towards FDA approval and opening overseas manufacturing sites, this Scottish born medical...
mindmatch.ai -
CY Partners-Newcastle upon Tyne
in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR or similar...
EPM Scientific-Newcastle upon Tyne
ensuring alignment with corporate objectives and regulatory requirements.Serve as a key medical expert, providing scientific support and guidance to internal teams, including clinical development, regulatory affairs, and commercial functions.Support...
mindmatch.ai -
CY Partners-Newcastle upon Tyne
in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR or similar...
SUN PHARMA-Newcastle upon Tyne
Job offer
For our dynamic growing, innovative Brands division in UK within an already established big generic International pharmaceutical company, we are looking for an outgoing experienced Senior Medical Affairs field professional who dares...
mindmatch.ai -
CY Partners-Newcastle upon Tyne
in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR or similar...
ADVANZ PHARMA-Newcastle upon Tyne
the Medical Affairs strategy, as discussed with management at a national level and approved by the Global Director Medical Affairs, through development and execution of a local MSL plan
• Contribute towards medical strategy for maintenance products and future...
joblookup.com -
1 similar job: London
Newcastle upon Tyne
in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR...
cv-library.co.uk -
CY Partners-Newcastle upon Tyne
Experience in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR...
mindmatch.ai -
CY Partners-Sunderland
Experience in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR...
Indegene-Newcastle upon Tyne
documentation, analysis and tracking of medical information documents.
• Work with the medical information and medical affairs teams during congresses, product launches, and key data releases and ensure assigned work is completed as per the timelines and SOPs...
mindmatch.ai -
CY Partners-Newcastle upon Tyne
in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR or similar...
Norgine-England
solutions.
We have an exciting opportunity for a Medical Advisor to join Norgine. The person holding this position will report to the Medical Director and be a member of the UK Medical Affairs team.
The core responsibility of the Medical Advisor and Final...
workable.com -
CY Partners-Newcastle upon Tyne
in quality assurance and regulatory affairs within the medical device, pharmaceutical or related industry.
• Possess a knowledge and understanding of Quality Management Systems (QMS) and standards and regulations according to ISO 13485 and IVDR or similar...
Michael Page-England
in Life Sciences or a related field
• Proven experience as a Regulatory Affairs & Quality professional within a medical device manufacturer or similar role
• Knowledge of legal and regulatory requirements within Software / AI as a medical device...
michaelpage.co.uk -
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