Production Supervisor
Merck Life Science
Date: 2 hours ago
City: Livingston
Contract type: Full time
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Your Role
We have an exciting opportunity for a Production Supervisor to join our team in Livingston. In this role you will ensure that all production operations are carried out in a correct & timely manner always observing appropriate practice, you will plan and allocate resources required to achieve the production plan. You will ensure that all relevant batch documentation has been completed satisfactorily following GMP and assist in the preparation and modification of company documentation, where necessary.
Key Responsibilities Include
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Your Role
We have an exciting opportunity for a Production Supervisor to join our team in Livingston. In this role you will ensure that all production operations are carried out in a correct & timely manner always observing appropriate practice, you will plan and allocate resources required to achieve the production plan. You will ensure that all relevant batch documentation has been completed satisfactorily following GMP and assist in the preparation and modification of company documentation, where necessary.
Key Responsibilities Include
- Ensure that all areas are maintained to a high, clean standard and all operations are logged correctly.
- Manage and record personnel issues relating to operators, with regard to induction, holidays, overtime, etc. Assist in the training of operators.
- Initiate and progress investigative documentation within the working areas.
- In the absence of the Production Manager, you will deputise where required by liaising with other departments.
- Update and maintain electronic spreadsheets, databases and planning systems as appropriate.
- Provide reports to the Production Manager as required.
- Previous experience in lead/supervisory role (directly and/or indirectly) and working to GMP standards within a regulated environment.
- Experience of working with red cell products would be desirable.
- Good organisation skills to plan through-put and allocation of operators.
- Good computer skills to ensure operation of the Company electronic systems and relevant databases.
- Excellent verbal, written and interpersonal communication skills.
- Ability to meet deadlines and targets.
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
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