At a Glance
- Tasks: Conduct quality control testing and support manufacturing operations in a dynamic lab environment.
- Company: Join a growing team in a regulated manufacturing setting focused on quality and innovation.
- Benefits: Gain exposure to diverse analytical techniques and ongoing professional development opportunities.
- Other info: Flexible working hours with occasional weekend shifts and potential relocation support.
- Why this job: Make a real impact by ensuring high-quality products in a collaborative team.
- Qualifications: 1+ years in a lab, knowledge of GMP, and strong analytical skills.
The predicted salary is between 40500 - 49500 £ per year.
- QC Analyst
- Full-Time | Monday to Friday (9:00am - 5:00pm)
About the Role
We are seeking a motivated and detail-oriented QC Analyst to join a growing Quality Control team within a regulated manufacturing environment.
This is an excellent opportunity for someone with experience in pharmaceutical, biotechnology, or fine chemical laboratories who is looking to broaden their technical expertise and develop their career within a quality-focused business.
Working as part of a close-knit team of analysts, you will support manufacturing operations through the testing of raw materials, intermediates, and finished products, while also contributing to environmental monitoring, stability studies, and continuous improvement initiatives.
The role offers exposure to a wide range of analytical techniques and technologies, providing an excellent platform for ongoing development.
- What You'll Be Responsible For
- Quality Control Testing
- Perform testing of raw materials, intermediates, in-process samples, and finished products in accordance with approved procedures.
- Support manufacturing and customer delivery schedules through timely completion of analytical testing.
- Conduct testing associated with stability studies and product quality programmes.
- Review and interpret analytical data, ensuring compliance with GMP requirements.
- Analytical Techniques
- Generate and analyse data using a variety of analytical methods, including:
- HPLC
- GC
- AKTA systems
- TLC
- UV-Visible Spectroscopy
- Titration techniques
- Flow Cam
Apply strong technical and troubleshooting skills to resolve analytical issues and support investigations.
Microbiology & Environmental Monitoring
Carry out environmental monitoring activities, including
- Cleanroom monitoring
- Contact plates
- Viable and non-viable monitoring
- Luminometer testing
Conduct microbiological testing, including
- Bioburden testing
- Endotoxin testing
Support monitoring of purified water systems and controlled environments.
Quality & Compliance
Maintain accurate and compliant laboratory records in line with GMP and Quality Management System requirements.
Support investigations relating to
- Deviations
- Out-of-Specification (OOS) results
- Change controls
- Corrective and Preventive Actions (CAPAs)
Ensure compliance with pharmacopoeial requirements, ICH guidelines, and laboratory procedures.
Laboratory Operations
Support routine laboratory activities including
- Equipment calibration and maintenance
- Reagent preparation
- Inventory management
- Purchasing consumables
- Documentation and archiving
Work collaboratively with manufacturing, R&D, technology transfer, and external laboratory partners.
About You
You are a quality-focused laboratory professional who enjoys analytical problem-solving, working in a regulated environment, and contributing to the delivery of high-quality products.
You'll bring
- At least 1 year's experience working within a pharmaceutical, biotechnology, or fine chemical laboratory.
- A good understanding of GMP and Quality Management Systems.
- Experience with analytical testing and laboratory techniques.
- Strong attention to detail and an organised approach to documentation and compliance.
- Excellent problem-solving and technical troubleshooting skills.
- Strong IT, analytical, and numerical capabilities.
- Particularly Relevant Experience
- HPLC analysis
- Microbiological testing
- Environmental monitoring
- Stability studies
- AKTA systems
- Endotoxin and bioburden testing
- Laboratory investigations and GMP documentation
- Personal Attributes
We're looking for someone who is
- Positive and team-oriented
- Comfortable working independently and as part of a team
- Proactive and willing to learn
- Flexible and adaptable
- Confident communicating with colleagues across different departments
- Happy to support occasional overtime or weekend work when required
Why Join Us?
- Join a supportive and collaborative team environment.
- Gain exposure to a wide range of analytical and microbiological techniques.
- Work across quality control, manufacturing support, and product development activities.
- Access ongoing training and professional development opportunities.
- Be part of a business that values quality, innovation, and continuous improvement.
- Location & Working Pattern
- Monday to Friday, 9:00am - 5:00pm
- Primarily laboratory-based role (approximately 80% lab, 20% office)
- Occasional weekend working on a rotational basis to support business requirements
- Relocation support may be available for the right candidate
The Opportunity
This is an excellent opportunity for an analyst with experience in chemistry, microbiology, or pharmaceutical quality control to join a friendly and highly collaborative team.
Whether your strengths lie in HPLC, microbiology, or a broader analytical background, you'll have the opportunity to develop your skills across multiple areas while contributing to the manufacture and release of high-quality products.
QC Analyst employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
StudySmarter Expert Advice🤫
We think this is how you could land QC Analyst
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like SRG. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like SRG.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like SRG. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what SRG is looking for. A tailored application can really make you stand out!
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at SRG!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show SRG that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at SRG!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At SRG, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at SRG
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at SRG that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with SRG’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
