At a Glance
- Tasks: Conduct microbiological testing and ensure product quality in a fast-paced lab.
- Company: Leading pharma/biotech company with strong scientific standards.
- Benefits: Competitive day rate and exposure to cutting-edge QC practices.
- Other info: Gain valuable experience in a GMP-regulated environment.
- Why this job: Join a collaborative team and make a real impact on product quality.
- Qualifications: Degree in Microbiology or related field, with hands-on lab experience.
The predicted salary is between 30000 - 40000 £ per year.
This is a contract role within a regulated pharmaceutical/biotech QC laboratory, focused on supporting product quality, environmental monitoring, and GMP-compliant testing. The position requires strong laboratory experience in both microbiology and QC testing, with a focus on generating accurate, reliable, and compliant data in a fast-paced environment.
Key Responsibilities
- Perform QC testing of raw materials, intermediates, and finished products
- Conduct microbiological testing including bioburden, sterility testing, and environmental monitoring
- Work in accordance with GMP/GLP standards and internal SOPs
- Investigate OOS/OOT results, deviations, and support laboratory investigations
- Review and document QC and microbiology data to ensure accuracy and compliance
Candidate Profile
- Degree in Microbiology, Biology, Chemistry, or related discipline
- Experience in a pharmaceutical, biotech, or CRO QC laboratory environment
- Hands-on experience with microbiology techniques (bioburden, sterility, EM)
- Strong understanding of GMP environments and aseptic practices
- High attention to detail and ability to work in a structured environment
What’s on Offer
- Contract role in a leading pharma/biotech QC environment
- Exposure to both microbiology and quality control testing
- GMP-regulated laboratory with strong scientific standards
- Collaborative team environment
- Competitive day rate (based on experience)
Quality Control Scientist employer: Barrington James Limited
As a Quality Control Scientist in our leading pharmaceutical/biotech QC laboratory, you will thrive in a collaborative and dynamic environment that prioritises scientific excellence and compliance. We offer competitive day rates, opportunities for professional growth, and the chance to work with cutting-edge technologies while ensuring product quality and safety. Join us to be part of a team that values accuracy, reliability, and innovation in a GMP-regulated setting.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Scientist
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like Barrington James Limited.
We think you need these skills to ace Quality Control Scientist
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Barrington James Limited.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Barrington James Limited. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Barrington James Limited
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Barrington James Limited.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Barrington James Limited achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
