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- Tasks: Conduct QC testing and inspections for vaccine manufacturing and ensure compliance with regulations.
- Company: Join a leading global biopharmaceutical organisation in Liverpool.
- Benefits: Gain valuable experience in a dynamic industry with potential for career growth.
- Why this job: Make a difference in vaccine production while developing your skills in a vital field.
- Qualifications: Experience in QC testing and knowledge of cGMP standards required.
- Other info: 6-month contract with opportunities to contribute to critical health initiatives.
The predicted salary is between 30000 - 40000 £ per year.
We are supporting a global biopharmaceutical organisation based in Liverpool in the search for an experienced QC Analyst to join their Quality Control team on a 6-month contract. This role will focus on the compliant execution of QC testing, inspection, and release activities across both bioassay and incoming materials/components, supporting critical vaccine manufacturing operations. You will also contribute to technical and validation studies, ensuring alignment with both departmental and site objectives.
Key Responsibilities
- Perform QC testing on in-process, intermediate, and finished vaccine products
- Conduct data review and interpretation in line with approved SOPs
- Ensure all work is carried out in compliance with cGMP and regulatory standards
- Accurately document all laboratory activities, ensuring data integrity
- Support method validation, transfer, and technical studies
- Perform primary QC inspection and sampling of raw materials
- Conduct testing of primary and secondary packaging components
- Review and interpret analytical data in accordance with SOPs
- Support the release of raw materials and components for manufacturing
- Assist in deviations, investigations, and CAPA activities
Requirements
- Fluent in English (written and verbal)
- Proven experience in QC testing techniques relevant to the role (bioassay and/or raw materials/components testing)
- Strong experience working within a cGMP-regulated environment
- Clear understanding of GMP compliance, documentation, and data integrity principles
- Aware of equipment qualification and method validation requirements
- Understanding of root cause analysis and its application within investigations
- Strong IT skills with experience using electronic laboratory and quality systems (e.g. LIMS, electronic documentation systems)
- Demonstrable experience working within the pharmaceutical or biopharmaceutical industry under cGMP conditions
QC Bioassay Analyst in Liverpool employer: Adepto Technical Recruitment Ltd
Contact Detail:
Adepto Technical Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Bioassay Analyst in Liverpool
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical industry, especially those who work in QC. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of cGMP and QC testing techniques. We recommend practising common interview questions related to bioassay and raw materials testing to show you’re the right fit.
✨Tip Number 3
Don’t forget to showcase your experience with electronic lab systems like LIMS during interviews. We want to see how you can bring your tech skills to the table and improve our quality control processes.
✨Tip Number 4
Apply through our website for the best chance at landing that QC Bioassay Analyst role. It’s the quickest way to get your application in front of the right people and show us you mean business!
We think you need these skills to ace QC Bioassay Analyst in Liverpool
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in QC testing techniques, especially in bioassay and raw materials/components. We want to see how your skills align with the job description, so don’t be shy about showcasing relevant projects or roles you've had!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your background fits perfectly with our needs. We love seeing enthusiasm and a clear understanding of the QC processes involved in vaccine manufacturing.
Showcase Your Compliance Knowledge: Since this role is all about cGMP compliance, make sure to mention your experience working in regulated environments. We’re looking for candidates who understand GMP compliance, documentation, and data integrity principles, so highlight any relevant experiences you have!
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 gives you a chance to explore more about our company and culture!
How to prepare for a job interview at Adepto Technical Recruitment Ltd
✨Know Your QC Basics
Make sure you brush up on your knowledge of QC testing techniques, especially those related to bioassays and raw materials. Be ready to discuss specific methods you've used and how they align with cGMP standards.
✨Familiarise Yourself with SOPs
Since you'll be working with standard operating procedures (SOPs), it’s crucial to understand them inside out. Prepare examples of how you've adhered to SOPs in past roles, particularly in a regulated environment.
✨Showcase Your Data Integrity Skills
Data integrity is key in this role. Be prepared to talk about how you've ensured data accuracy and compliance in your previous positions. Highlight any experience with electronic laboratory systems like LIMS.
✨Prepare for Technical Questions
Expect technical questions related to method validation and root cause analysis. Brush up on these topics and think of scenarios where you've applied these principles in your work. This will show your depth of knowledge and problem-solving skills.