Biologics Manufacturing Assistant
1 month ago
We are seeking a highly skilled Biologics Manufacturing Assistant to join our Operations Department in Keele, Staffordshire. As a key member of our team, you will be responsible for the support and maintenance of our GMP facility, ensuring compliance with current Good Manufacturing Practice (GMP) standards.
Key Responsibilities- Maintenance of the GMP facility, including daily and campaign cleaning, to ensure a safe and efficient working environment.
- Compliant completion of GMP documentation, including accurate and timely recording of activities and results.
- Preparation and autoclaving of materials for GMP contracts, ensuring adherence to quality and regulatory requirements.
- Performance of autoclave performance testing, to ensure equipment is functioning correctly and safely.
- Transfer of materials and equipment as part of project start-up activities, to facilitate smooth operations.
- Management of small equipment calibration and re-calibration, to ensure accuracy and precision.
- Flexibility to support teams delivering scientific processes within the GMP facility, to meet business needs.
- Adherence to proper compliance with Health and Safety of all operations within the team, in accordance with the Health, Safety and Environmental policies and procedures.
- Allocation of timesheet codes for assigned programs of work and in-house activities, to ensure accurate tracking and reporting.
To be successful in this role, you will need to demonstrate strong written and verbal communication skills, ideally with 5 or more GCSEs (or equivalent) at grade A-C/4-9, including English Language and Mathematics.
You will also need to be self-motivated, enjoy working in a busy environment, and be adaptable to work alone or as part of a team. Strong organizational skills and ability to follow instructions to meet timelines are essential. Practical experience in a laboratory environment would be an advantage, but full training will be provided.
About Charles River LaboratoriesCharles River Laboratories is a global contract research organization (CRO) providing a range of services to support the development of new medicines. Our mission is to improve the quality of people's lives by helping to bring life-saving therapies to market faster. We are committed to diversity and inclusion, and we recognize and recruit all talent.
For more information, please visit our website.
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Biologics Manufacturing Assistant
1 month ago
Keele, United Kingdom Charles River Laboratories, Inc. Full timeAbout the RoleWe are seeking a highly skilled and motivated Biologics Manufacturing Assistant to join our Operations Department in Keele, Staffordshire. As a key member of our team, you will be responsible for supporting and maintaining the GMP facility, ensuring compliance with current Good Manufacturing Practice (GMP) standards.Key...
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Biologics Manufacturing Assistant
1 month ago
Keele, United Kingdom Charles River Laboratories, Inc. Full timeAbout the RoleWe are seeking a highly skilled and motivated Biologics Manufacturing Assistant to join our Operations Department in Keele, Staffordshire. As a key member of our team, you will be responsible for supporting and maintaining the GMP facility, ensuring compliance with current Good Manufacturing Practice (GMP) standards.Key...
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4 weeks ago
Keele, United Kingdom Charles River Laboratories, Inc. Full timeAbout the RoleWe are seeking a highly skilled Biologics Manufacturing Assistant to join our Operations Department in Keele, Staffordshire. As a key member of our team, you will be responsible for the support and maintenance of our GMP facility, ensuring compliance with current Good Manufacturing Practice (GMP) standards.Key ResponsibilitiesMaintenance of the...
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Biologics Manufacturing Assistant
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Keele, United Kingdom Charles River Laboratories, Inc. Full timeAbout the RoleWe are seeking a highly skilled Biologics Manufacturing Assistant to join our Operations Department in Keele, Staffordshire. As a key member of our team, you will be responsible for the support and maintenance of our GMP facility, ensuring compliance with current Good Manufacturing Practice (GMP) standards.Key ResponsibilitiesMaintenance of the...
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