Select Pharma Jobs in United Kingdom

Job Description · An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. · Responsibilities: · Primarily responsible for post-approval and compliance acti ...

A pharmaceutical company in Greater London is seeking a Principal Regulatory Affairs Officer. The role involves providing full regulatory input for the submission and assessment of Marketing Authorisation Applications, ensuring compliance with UK and EU legislation. Candidates sh ...

Responsibilities Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications. Manages increasi ...

Job Description · Responsibilities: · Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applicati ...

Job Description · Within this role you will be responsible for leading and motivating the manufacturing team to deliver high-quality production. Supervise all manufacturing activities, monitor performance, allocate resources, ensure workflow meets packaging demands, maintain GMP ...

A leading pharmaceutical company in Sunbury-on-Thames seeks a Principal Regulatory Affairs Officer to provide regulatory input and support for product submissions. The role involves preparing and responding to questions for Marketing Authorisation Applications, with increasing co ...

A pharmaceutical company in Greater London is seeking a Principal Regulatory Affairs Officer. The role involves providing full regulatory input for the submission and assessment of Marketing Authorisation Applications, ensuring compliance with UK and EU legislation. Candidates sh ...

Job Description · An excellent opportunity has arisen for an experienced regulatory professional to join my client, an established Regulatory consultancy, on an initial 12 month contract basis - the contract can be on a 6 or 12 month basis, full time or part time and fully remote ...

Job Summary: · The Manufacturing Supervisor will lead and motivate the manufacturing team to deliver high-quality production by supervising all activities, monitoring performance, allocating resources, ensuring workflow meets packaging demands. · ...

Responsibilities · Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications. Manages increa ...