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- Tasks: Ensure quality standards in drug manufacturing and assist with quality-related issues.
- Company: Join Charles River, a leader in drug therapy development for 75 years.
- Benefits: Comprehensive training, career growth, and a chance to impact global health.
- Why this job: Make a difference in healthcare while building a fulfilling career.
- Qualifications: Experience in quality roles preferred, but training provided for the right candidate.
- Other info: Fast-paced environment with opportunities for teamwork and independent work.
The predicted salary is between 30000 - 40000 £ per year.
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.
Our Keele site is looking to recruit an Operational Quality Assurance Officer on a permanent, full time basis. The ideal candidate will have experience of working in a Quality role, to GMP standards but this is not essential as full comprehensive training will be provided to the successful candidate. This role is based in both the GMP manufacturing facility and office space working.
As part of the role you will need to have excellent attention to detail, have a proactive approach to problem solving, and be able to effectively communicate, both verbally and in writing. The role will require you 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.
Quality Assurance Officer 1 in Newcastle upon Tyne employer: Charles River Labs
Contact Detail:
Charles River Labs Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer 1 in Newcastle upon Tyne
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Charles River on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by brushing up on GMP standards and quality assurance processes. We recommend practising common interview questions and having examples ready that showcase your attention to detail and problem-solving skills.
✨Tip Number 3
Show your passion for the role! During interviews, express why you’re excited about contributing to drug therapies and how your skills align with the company’s mission. It’s all about making that personal connection.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take the initiative to engage directly with us.
We think you need these skills to ace Quality Assurance Officer 1 in Newcastle upon Tyne
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Quality Assurance Officer role. Highlight any relevant experience in quality roles or GMP standards, even if it’s just a small part of your background.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you’re passionate about quality assurance and how your proactive problem-solving skills can benefit our team. Be genuine and let your personality shine through!
Showcase Attention to Detail: Since this role requires excellent attention to detail, make sure your application is free from typos and errors. A polished application shows us you care about quality right from the start!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Charles River Labs
✨Know Your GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) standards, even if you haven't worked in a Quality role before. Understanding the basics will show your commitment to quality and help you answer questions confidently.
✨Showcase Your Attention to Detail
Prepare examples from your past experiences that highlight your attention to detail. Whether it's a project you managed or a problem you solved, being able to articulate how you caught errors or improved processes will impress the interviewers.
✨Practice Problem-Solving Scenarios
Think of potential quality-related issues that could arise in a GMP environment and how you would address them. Practising these scenarios will help you demonstrate your proactive approach to problem-solving during the interview.
✨Communicate Clearly and Confidently
Since effective communication is key for this role, practice articulating your thoughts clearly. Whether it’s through mock interviews or discussing your experiences with friends, being able to convey your ideas succinctly will make a great impression.