At a Glance
- Tasks: Execute quality control testing for vaccines and ensure compliance with industry standards.
- Company: Join a leading vaccine company making a global health impact.
- Benefits: Enjoy stock options, gym membership, and employee assistance programmes.
- Other info: Dynamic team environment with opportunities for growth and learning.
- Why this job: Be part of groundbreaking vaccine development and contribute to public health.
- Qualifications: Experience in QC labs and knowledge of GMP practices required.
The predicted salary is between 30000 - 40000 £ per year.
We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs. We have leveraged our expertise and capabilities both to commercialize three vaccines, including the world’s first and only chikungunya vaccine, and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease and Zika. With operations in Austria, Canada, France, Sweden, the United Kingdom, and the U.S., we are committed to making a positive impact on global public health. Together, we are a global Company which is open to people of all backgrounds. Our diverse and inclusive workforce makes Valneva a great place to work.
Our Quality Control team are now recruiting for a QC Technician (Analytical). Primary responsibility will be to execute defined and trained Quality Control department testing for the release of raw materials, intermediate products and final products according to defined procedures and protocols and according with best cGMP work practices, Quality Standards and metrics.
- Execute analytical procedures for testing of raw materials, intermediate products and final products, according to defined SOPs and protocols.
- Apply best cGMP work practices and techniques to test and release raw materials and product within defined specifications.
- Ensure that all necessary training is complete in the procedures conducted, and operate in compliance with best cGMP working practices at all times.
- Conduct on-time reporting according to the defined and trained document management standards including review and verification of analytical data.
- Immediately elevate and report any deviations to materials, facilities, processes or procedures to the Laboratory Manager.
- Be accountable for the analytical laboratories being clean, tidy and well organised and in a state of continuous inspection readiness.
- Conduct all activities in the most careful and safe manner and in full compliance with HSE requirements.
- Ensure that at any time equipment, facilities and materials used in the QC laboratories comply with defined standards.
- Support change controls, investigations and CAPA’s in the most diligent manner.
- Identify areas for continuous improvement and upscale those to the Head of QC.
- Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team setting.
- Maintain adequate stocks of materials and equipment and laboratory consumables.
- Assist in monitoring and maintaining calibration status of all equipment within the Quality Control department.
- Storage of in process, and final products samples including, for stability and retention purposes.
- Preparation of SOPs (where applicable) in accordance with Valneva Quality systems.
- Perform filing duties and other QC administrative duties as required by the Laboratory Manager.
- To undertake any other duties as requested by the Laboratory Manager/Senior Analyst in accordance with company requirements.
- Shift work and out of hours work as required, including weekend work.
Experience:
- Previous experience working within a QC laboratory working to GMP within a recognised quality system.
- Writing and working to SOP documentation.
- Analytical methods experience, in a production-focused environment, in assays (not limited to) Haemagglutination assays, micro-plate assays such as ELISA and dye binding colorimetric assays (Bradford Method, Coomassie Plus), Electrophoresis, TVC and UV Spectrophotometry.
- Assay development, validation and transfer experience desirable.
- Experience of working within Quality Management Systems which include deviations, change controls and CAPA’s.
- Cell culture and Microbiological experience would be preferable.
- Plaque testing and ELISA experience highly desirable.
- Proven track record of being able to maintain the highest standards of hygiene and cleanliness in a laboratory environment.
- All round experience of working within a laboratory environment.
Benefits:
- Stock Options
- Employee Assistance Programme
- Gym membership OR fitness allowance
- EV Salary Sacrifice
- Many others included
QC Technician (Analytical) - Livingston, United Kingdom employer: Valneva SE
Valneva SE is an excellent employer that prioritises employee development and fosters a collaborative work culture in the heart of a thriving biotech hub. With a commitment to innovation in vaccine quality, employees benefit from comprehensive training opportunities, competitive compensation, and a supportive environment that encourages continuous improvement and teamwork. Working here means being part of a mission-driven organisation dedicated to making a meaningful impact on global health.
StudySmarter Expert Advice🤫
We think this is how you could land QC Technician (Analytical) - Livingston, United Kingdom
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their mission and values, especially since they focus on public health. Tailor your answers to show how you can contribute to their goals.
✨Tip Number 3
Practice common interview questions and have your own ready. Think about how your experience with GMP and analytical methods aligns with what they’re looking for. Confidence is key!
✨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 are proactive and engaged with our company.
We think you need these skills to ace QC Technician (Analytical) - Livingston, United Kingdom
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the QC Technician role. Highlight your relevant experience in GMP environments and any analytical methods you've worked with. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about working in vaccine development and how your background makes you a great fit for our team. Keep it concise but impactful!
Showcase Your Attention to Detail:In the QC world, attention to detail is key. When filling out your application, make sure everything is accurate and well-organised. This reflects your ability to maintain high standards in a lab setting, which we value highly.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the info you need about the role and our company there!
How to prepare for a job interview at Valneva SE
✨Know Your GMP Basics
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Familiarise yourself with the key principles and how they apply to quality control in a laboratory setting. This will show that you understand the importance of compliance and can contribute to maintaining high standards.
✨Familiarise with Analytical Techniques
Since the role involves various analytical methods, it’s crucial to be well-versed in techniques like ELISA, electrophoresis, and spectrophotometry. Prepare to discuss your hands-on experience with these methods and any relevant assays you've worked on. This will demonstrate your technical expertise and readiness for the job.
✨Prepare for Scenario Questions
Expect questions about how you would handle specific situations, such as deviations from protocols or equipment malfunctions. Think of examples from your past experiences where you successfully navigated challenges in a QC environment. This will highlight your problem-solving skills and ability to work under pressure.
✨Show Your Team Spirit
Valneva values a collaborative environment, so be ready to talk about your experiences working in teams. Share examples of how you’ve contributed to a positive team dynamic or supported colleagues in achieving common goals. This will reflect your fit within their inclusive culture.
