Operations Management part time jobs in £40,000 - £50,000
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Ofgem works on behalf of energy consumers to ensure that every household and business in the UK can rely on a safe, affordable and environmentally ...
This is a fantastic opportunity for a driven individual with an experienced and diverse background in corporate research, market research or business
Policy Designers will lead and support a range of policy development projects with design, data, and digital tools at their core.
As a CMC Regulatory Project Manager, you will responsible for a portfolio of biopharmaceuticals and Cell & Gene Therapy products.
We have an exciting opportunity available in our Regulatory Affairs Management team.
This is an opportunity to join the Pharma Supply Quality Assurance group within R&D at GSK Harlow.
We are seeking a highly motivated and experienced Regulatory Affairs professional to join our expanding Devices group within Global..
The Contract Manager will ensure there are clear management controls for governance, performance management, business communication
This position is a key partner to the Consumer Health supply chain, leading audits and compliance in Good Manufacturing Practice..
We are currently recruiting for a Technical Site Operations Manager to support the delivery of World Class facilities that are safe.....
The Chief of Staff is a key leadership role within the R&D Operations organization reporting into the Head of R&D Operations and supporting
This role ensures GSK's global energy and utility strategies and initiatives have the privilege of focus to ensure delivery.
This role ensures GSK's global sustainability strategies and initiatives have the privilege of focus to ensure delivery.
The role is responsible for the leadership of a team focused on defining and driving the GCI/EM regulatory policy, advocacy and intelligence
In this role you will lead operations for Value Evidence and Outcomes (VEO).
Ensure the development of appropriate regional regulatory strategy(s) and their execution for assigned asset(s) consistent with Medicines Development
The Regulatory Project Manager is responsible for the timely production of approved documentation for clinical trials and marketing applications