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- Tasks: Join a dynamic team as a Biologics Manufacturing Operator, executing vital manufacturing processes.
- Company: Charles River is a leading contract research organisation dedicated to improving global health.
- Benefits: Enjoy a collaborative work environment with opportunities for career growth and development.
- Why this job: Make a real impact on drug therapies while working in a supportive and innovative culture.
- Qualifications: Minimum HNC/HND in a science subject; previous lab experience is a plus.
- Other info: Diversity and inclusion are core values at Charles River, welcoming all talent.
The predicted salary is between 28800 - 43200 £ per year.
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Biologics Manufacturing Operator, Newcastle
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Client:
Location:
Newcastle, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
dca5842b6d72
Job Views:
6
Posted:
16.07.2025
Expiry Date:
30.08.2025
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Job Description:
For 75years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
Job Summary
Our manufacturing site in Keele, is offering an opportunity for an upstream Biologics Manufacturing Operator.
Job alert service
Responsible for the execution of assigned work of in house and contracted programmes of work for the development, transfer or cGMP Manufacture of processes as assigned to them.
What You\’ll Be Doing:
Responsibilities will include: participating in multidisciplinary teams for assigned work ensuring that all allocated activities are executed in a timely manner according to schedules set and ensuring that operational, quality and Health & Safety targets are met as required by the Company.
- To execute and complete assigned programmes of work both in house and contractually in a timely manner.
- To record data and communicate results through verbal and written work.
- To ensure that all operations and procedures are performed after appropriate training; that training is maintained for performing all operations and procedures and regularly updated in job training manuals.
- To actively maintain the execution of 5S system of facility management.
- To ensure laboratory notebooks, Process Development and Production documentation is completed in a timely manner and maintained to high standards as per Company
- To form part of multidisciplinary teams working within all areas of the Operations Group.
- 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 ensure consideration for cGMP needs are met when developing processes.
Skills and Experience:
- Minimum HNC/HND in a science subject or equivalent and / or Degree in Biochemistry, Biotechnology, Biochemical Engineering or equivalent qualification.
- Previous practical laboratory experience is desirable.
- 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.
About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.
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 over 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 80% of the drugs approved by the FDA in the last five years.
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.
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Created on 16/07/2025 by TN United Kingdom
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Biologics Manufacturing Operator employer: Charles River Laboratories, Inc.
Contact Detail:
Charles River Laboratories, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Biologics Manufacturing Operator
✨Tip Number 1
Familiarise yourself with current Good Manufacturing Practice (cGMP) standards, as this role heavily relies on compliance with these regulations. Understanding the nuances of cGMP will not only help you in interviews but also demonstrate your commitment to quality and safety in manufacturing.
✨Tip Number 2
Network with professionals in the biologics and pharmaceutical industries. Attend relevant conferences or webinars, and connect with employees from Charles River on platforms like LinkedIn. This can provide insights into the company culture and potentially lead to referrals.
✨Tip Number 3
Showcase your practical laboratory experience during any discussions or interviews. Be prepared to discuss specific techniques or projects you've worked on that relate to biologics manufacturing, as this will highlight your hands-on skills and readiness for the role.
✨Tip Number 4
Demonstrate your ability to work in multidisciplinary teams by sharing examples from your past experiences. Highlighting your teamwork skills will resonate well with the collaborative nature of the role at Charles River, making you a more attractive candidate.
We think you need these skills to ace Biologics Manufacturing Operator
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience and skills that align with the Biologics Manufacturing Operator role. Emphasise any laboratory experience, teamwork, and compliance with cGMP standards.
Craft a Strong Cover Letter: Write a cover letter that showcases your passion for the role and the company. Mention specific reasons why you want to work at Charles River and how your background in life sciences makes you a great fit.
Highlight Communication Skills: Since strong written and verbal communication skills are essential for this position, provide examples in your application of how you've effectively communicated results or collaborated within teams in previous roles.
Showcase Initiative and Flexibility: In your application, demonstrate your ability to be a self-starter and a team player. Share instances where you've taken the initiative or adapted to changing circumstances in a work environment.
How to prepare for a job interview at Charles River Laboratories, Inc.
✨Understand cGMP Standards
Familiarise yourself with current Good Manufacturing Practice (cGMP) standards, as they are crucial for the role. Be prepared to discuss how you have adhered to these standards in previous experiences or how you would ensure compliance in your work.
✨Showcase Teamwork Skills
Since the role involves working within multidisciplinary teams, highlight your ability to collaborate effectively. Share examples of past team projects and your contributions to achieving common goals.
✨Demonstrate Communication Skills
Strong written and verbal communication skills are essential. Prepare to discuss how you have communicated complex information clearly in previous roles, whether through reports, presentations, or team discussions.
✨Prepare for Practical Questions
Expect practical questions related to laboratory procedures and data recording. Brush up on your technical knowledge and be ready to explain your approach to problem-solving in a lab environment.
