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- Tasks: Support and maintain a GMP facility, ensuring cleanliness and compliance.
- Company: Join Charles River Laboratories, a leader in drug development and improving lives globally.
- Benefits: Enjoy career growth opportunities, a supportive team, and a chance to make a real impact.
- Why this job: Be part of a mission-driven company that helps bring life-saving therapies to market faster.
- Qualifications: Minimum 5 GCSEs including English and Maths; lab experience is a plus.
- Other info: Flexible working environment with a focus on teamwork and innovation.
The predicted salary is between 30000 - 42000 ÂŁ per year.
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At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
Job Summary
Our manufacturing site in Keele, is offering an opportunity for a Biologics Manufacturing Associate.
Responsible for the support and maintenance of the GMP facility. Responsibilities will include; daily and campaign cleaning within the GMP facility, ensuring that operational, quality and Health & Safety targets are met as required by the Company.
To ensure that all activities performed are in line with the Code of Conduct.
What You’ll Be Doing
- Maintenance of the GMP facility including daily and campaign cleaning.
- Compliant completion of GMP documentation.
- Materials preparation and autoclaving for GMP contracts.
- Responsibility for performing autoclave performance testing.
- Materials and equipment transfer as part of project start up activities.
- Responsibility for the management of small equipment calibration/re-calibration.
- Working flexibly to support the teams delivering scientific processes within the GMP facility.
- To perform manufacturing operations within the appropriate current Good Manufacturing Practice (cGMP) standards, ensuring compliance is maintained, as defined in the Company Quality system.
- To adhere to proper compliance with Health and Safety of all operations within the team, in accordance with the Health, Safety and Environmental policies and procedures.
- To work within the companies policies for timesheet allocation codes for assigned programmes of work and in house activities.
- Perform other duties that from time-to-time management will assign.
Skills And Experience
- Education: Minimum 5+ GCSE grade A-C including English Language and Mathematics or equivalent qualification.
- Experience: Previous practical laboratory experience is desirable.
- Other: Able to demonstrate strong written, verbal communication skills and practical skills. A self-starter, who shows initiative and is a team player. Able to work flexibly.
Profile And Requirements
About Corporate Functions
The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.
For more information, please visit www.criver.com.
229105
Seniority level
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Seniority level
Entry level
Employment type
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Employment type
Full-time
Job function
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Job function
Science
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Industries
Automation Machinery Manufacturing
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Biologics Manufacturing - Associate employer: Charles River Laboratories
Contact Detail:
Charles River Laboratories Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Biologics Manufacturing - Associate
✨Tip Number 1
Familiarise yourself with Good Manufacturing Practice (GMP) standards, as this role heavily involves compliance with these regulations. Understanding the principles of GMP will not only help you in the interview but also demonstrate your commitment to quality and safety in manufacturing.
✨Tip Number 2
Highlight any previous laboratory experience you have, even if it's not directly related to biologics. Be prepared to discuss specific tasks you've performed that relate to cleaning, equipment calibration, or documentation, as these are key responsibilities in the role.
✨Tip Number 3
Showcase your ability to work as part of a team. This position requires collaboration with various departments, so be ready to share examples of how you've successfully worked in teams in the past, especially in high-pressure environments.
✨Tip Number 4
Research Charles River Laboratories and their mission to improve lives through drug development. Being knowledgeable about the company’s values and recent achievements can help you stand out during interviews and show your genuine interest in being part of their team.
We think you need these skills to ace Biologics Manufacturing - Associate
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Biologics Manufacturing - Associate position. Understand the key responsibilities and required skills, such as GMP compliance and laboratory experience.
Tailor Your CV: Customise your CV to highlight relevant experience and skills that align with the job requirements. Emphasise any previous laboratory work, compliance with health and safety standards, and your ability to work in a team.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the company. Mention how your background and skills make you a great fit for Charles River Laboratories and their mission to improve lives.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail.
How to prepare for a job interview at Charles River Laboratories
✨Understand GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) standards, as this role heavily involves compliance with these regulations. Be prepared to discuss how you would ensure adherence to these practices in your daily tasks.
✨Showcase Your Laboratory Experience
If you have previous practical laboratory experience, make sure to highlight it during the interview. Discuss specific tasks you've performed that relate to the responsibilities of the Biologics Manufacturing Associate role.
✨Demonstrate Teamwork and Initiative
Charles River values self-starters who can work well in a team. Prepare examples of how you've successfully collaborated with others in past roles and how you took the initiative to solve problems.
✨Communicate Clearly
Strong written and verbal communication skills are essential for this position. Practice articulating your thoughts clearly and concisely, especially when discussing technical topics related to biologics manufacturing.
