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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.
We are currently looking to recruit a Operational Quality Assurance Officer to work in the Quality Assurance department at our Keele facility. The ideal candidate will have experience working within a GMP Grade C cleanroom environment.
As part of the role you will need to have excellent attention to detail, have a pro active approach to problem solving, be able to effectively communicate, both verbally and in writing. The role will require you to be able to manage priorities whilst working both as part of a team and independently in a fast paced environment.
The main duties will include:
• Provide ‘in suite’ operational QA oversight and assistance on quality related issues within the GMP manufacturing Grade D and Grade C Facility.
• Provide Facility Systems support, including review and approval of HVAC Pressures, Temperature, and Cleaning Logs,
• Perform ‘in suite’ Room Inspections and Release.
• Issue, review and approval of GMP batch manufacturing records to support QP certification and release.
• Assist in performance of internal self-inspection audits
• Generation, review and approval of relevant quality documentation
• Support with assessment of deviation event investigations
• Support closure to plan of Change Controls and CAPA actions.
• Assist and lead continuous improvement projects
• Review and approval of Validation reports.
• Archiving of operational and quality control documentation
Education / Experience:
Ideally Science degree or equivalent, with proven relevant experience in a pharmaceutical Manufacturing or Quality Assurance role.
Minimum requirement science related A level with 2 years experience in an operational Quality Assurance role. You will have good working knowledge of GMP, ideally in the pharmaceutical sector but this is not essential.
This role will be based at Keele, Staffordshire.
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.
Great News! We've discovered an exciting live job opportunity for a Quality Assurance Officer position in Keele. This job is currently open for hiring/recruiting by Charles River Laboratories, Inc., exclusively for you at UK Jobs. Feel free to download the job details here.
The work culture at Charles River Laboratories, Inc. must adhere to the Ethics of Work Culture as described in the Ethical framework of the UN Charter. You can gain more insights into their local workplace environment by exploring their jobs Charles River Laboratories, Inc. and also by visiting their official website through Google.
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Yes, we found live job(s) for Charles River Laboratories, Inc. in Keele.
Quality Assurance Officer jobs are available in United Kingdom.
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The average salary range for Quality Assurance Officer in Keele varies, but the standard pay scale is rated "Standard" in Keele. Salary levels may vary depending on your industry, experience, and skills. It's essential to research and negotiate effectively.
To apply for a job at Charles River Laboratories, Inc. follow the application process following the "Apply Now" button at UK Jobs and also you can visit Charles River Laboratories, Inc. official career page and follow their application process.
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