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- Tasks: Join a team to manufacture biologics and ensure quality standards are met.
- Company: Charles River Laboratories is a global leader in drug development and safety assessment.
- Benefits: Enjoy a full-time role with opportunities for career growth and a supportive work environment.
- Why this job: Make a real impact on global health while working in a dynamic, collaborative setting.
- 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.
The predicted salary is between 30000 - 42000 £ per year.
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For 75 years, 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.
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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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
Production
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Industries
Automation Machinery Manufacturing
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Biologics Manufacturing Operator employer: Charles River Laboratories
Contact Detail:
Charles River Laboratories 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
Highlight any practical laboratory experience you have, especially in biologics or related fields. If you've worked with multidisciplinary teams before, be sure to mention this, as teamwork is a key aspect of the role.
✨Tip Number 3
Prepare to discuss your problem-solving skills and how you've shown initiative in past roles. This position requires a self-starter attitude, so examples of how you've taken charge or improved processes will resonate well with the hiring team.
✨Tip Number 4
Research Charles River Laboratories and their contributions to drug development. Being knowledgeable about the company’s mission and recent projects can set you apart during interviews, showing that you're genuinely interested in being part of their team.
We think you need these skills to ace Biologics Manufacturing Operator
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Biologics Manufacturing Operator position. Tailor your application to highlight relevant skills and experiences that align with the job description.
Highlight Relevant Experience: If you have previous laboratory experience or qualifications in Biochemistry, Biotechnology, or related fields, be sure to emphasise these in your CV and cover letter. Use specific examples to demonstrate your practical skills and how they relate to the role.
Showcase Communication Skills: Since strong written and verbal communication skills are essential for this role, include examples in your application that showcase your ability to communicate effectively. This could be through previous work experiences, projects, or presentations.
Tailor Your CV and Cover Letter: Customise your CV and cover letter for the application. Use keywords from the job description and ensure that your documents reflect your enthusiasm for the role and the company. Make it clear why you want to join Charles River Laboratories and how you can contribute to their mission.
How to prepare for a job interview at Charles River Laboratories
✨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 would ensure compliance in your work and any relevant experiences you have had in similar environments.
✨Showcase Teamwork Skills
Since the role involves working within multidisciplinary teams, highlight your ability to collaborate effectively. Share examples of past experiences where you successfully worked as part of a team to achieve a common goal.
✨Demonstrate Communication Skills
Strong written and verbal communication skills are essential. Prepare to discuss how you have effectively communicated results and data in previous roles, and be ready to demonstrate these skills during the interview.
✨Prepare for Practical Questions
Expect questions that assess your practical laboratory experience and problem-solving abilities. Think about specific scenarios where you had to apply your knowledge in a lab setting and be ready to explain your thought process.
