At a Glance
- Tasks: Join our team as a QC Analyst, performing tests in a regulated lab.
- Company: Work with a global pharmaceutical leader in sterile injectable products.
- Benefits: Enjoy a competitive rate of £14.37 p/h and a 4 on, 4 off shift schedule.
- Why this job: Perfect for Biological Science grads looking to kickstart their career in biosafety.
- Qualifications: Must have a biological background and experience with cell cultures.
- Other info: Opportunity to work until December 2025 with potential for growth.
Job Title: QC Analyst – Biosafety Location: Speke, Liverpool. Contract: Until Oct Rate: £14.37 p/h (inclusive of shift uplift) Shift: 4 days on, 4 days off. 7am – 7pm.SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some GMP experience to further their career. Main responsibilities: Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations. Performing routine QC testing Documenting laboratory results in an accurate and timely manner. Complying with GMP regulatory requirements at all times. Key requirements: Experience of working to GMP/pharmaceutical regulatory requirements is desirable Experience within cell cultures required – roughly 6 months Biological background either from university degree or relevant work in the field Computer skills, excel, word, outlook Preferrable LIMS and SAP Carbon60, Lorien & SRG – The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
QC Analyst - Biosafety employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst - Biosafety
✨Tip Number 1
Make sure to highlight any experience you have with GMP regulations in your conversations. This is a key requirement for the QC Analyst role, and demonstrating your familiarity with these standards can set you apart from other candidates.
✨Tip Number 2
If you have experience with cell cultures, be prepared to discuss specific techniques or projects you've worked on. This will show your practical knowledge and help you connect with the team during interviews.
✨Tip Number 3
Familiarize yourself with the company’s products and their impact on public health, especially regarding flu treatments. Showing that you understand their mission can demonstrate your genuine interest in the role.
✨Tip Number 4
Brush up on your computer skills, particularly in Excel and LIMS. Being able to discuss how you’ve used these tools in past roles can give you an edge in the technical aspects of the job.
We think you need these skills to ace QC Analyst - Biosafety
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the QC Analyst - Biosafety position. Highlight the key responsibilities and requirements, such as GMP experience and cell culture knowledge, to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasize any relevant experience you have in Quality Control, particularly in a GMP environment. Mention specific tasks you've performed that align with the responsibilities listed in the job description.
Showcase Your Education: As a Biological Science graduate, make sure to detail your educational background. Include any relevant coursework or projects that demonstrate your understanding of biosafety and quality control processes.
Proofread Your Application: Before submitting your application, carefully proofread your documents for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a QC role.
How to prepare for a job interview at SRG
✨Show Your GMP Knowledge
Make sure to highlight your understanding of Good Manufacturing Practices (GMP) during the interview. Be prepared to discuss any previous experiences you have had working in a GMP-regulated environment, as this will demonstrate your suitability for the role.
✨Discuss Your Cell Culture Experience
Since experience with cell cultures is a key requirement, be ready to talk about your hands-on experience in this area. Share specific examples of techniques you've used and any challenges you've overcome while working with cell cultures.
✨Prepare for Technical Questions
Expect technical questions related to biosafety and quality control testing. Brush up on relevant testing methods and regulations, and be ready to explain how you would approach various scenarios in the lab.
✨Demonstrate Your Computer Skills
As the role requires proficiency in computer skills, particularly in Excel, Word, and Outlook, be prepared to discuss how you have used these tools in your previous roles. If you have experience with LIMS or SAP, make sure to mention that as well.