Biologics Manufacturing Operator

Job Description

This job is with Charles River, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
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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