At a Glance
- Tasks: Execute quality control testing for raw materials and products in a dynamic lab environment.
- Company: Join a leading vaccine company making a global health impact.
- Benefits: Enjoy stock options, gym membership, and employee assistance programmes.
- Other info: Collaborative team culture 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.
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 in accordance with best cGMP work practices, Quality Standards and metrics. 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.
Requirements
- 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 elevate 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) in Livingston employer: Valneva
Valneva is an exceptional employer, offering a dynamic and inclusive work environment where employees are empowered to make a meaningful impact on global public health through innovative vaccine development. With a strong commitment to employee growth, we provide comprehensive training, stock options, and wellness benefits, fostering a culture of collaboration and continuous improvement. Located in the UK, our state-of-the-art facilities ensure that our QC Technicians work in a clean, safe, and supportive atmosphere, making it an ideal place for those passionate about quality control in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land QC Technician (Analytical) in Livingston
✨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 practising common questions and showcasing your analytical skills. Be ready to discuss your experience with SOPs and cGMP practices, as these are key in the QC field.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and interests, like us at Valneva. Check our website regularly for openings and apply directly to stand out!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can leave a lasting impression and show your enthusiasm for the role. Plus, it keeps you on their radar as they make their decision.
We think you need these skills to ace QC Technician (Analytical) in Livingston
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the QC Technician role. Highlight your experience with analytical methods and any previous work in a GMP environment. We want to see how your skills match what we're looking for!
Showcase Your Attention to Detail:In your application, emphasise your ability to maintain high standards of hygiene and cleanliness in a lab setting. Mention specific examples where you’ve ensured compliance with quality standards, as this is crucial for us at StudySmarter.
Be Clear and Concise:When writing your cover letter, keep it clear and to the point. Explain why you're passionate about working in quality control and how you can contribute to our mission of improving global public health. We love straightforward communication!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, we love seeing candidates who take that extra step!
How to prepare for a job interview at Valneva
✨Know Your SOPs
Familiarise yourself with the Standard Operating Procedures (SOPs) relevant to the QC Technician role. Be prepared to discuss how you’ve applied these in previous positions, especially in relation to cGMP practices. This shows you understand the importance of compliance and quality standards.
✨Showcase Your Analytical Skills
Be ready to talk about your experience with analytical methods like ELISA, electrophoresis, or any assays you've worked with. Bring examples of how you’ve successfully executed these tests and any challenges you overcame. This will demonstrate your technical expertise and problem-solving abilities.
✨Emphasise Team Collaboration
Since the role involves working within a team, highlight your ability to contribute to a supportive and collaborative environment. Share specific instances where you’ve worked well with others, perhaps during investigations or CAPA processes, to show you’re a team player.
✨Prepare for Scenario Questions
Expect questions that assess your response to deviations or unexpected results in the lab. Think of examples from your past experiences where you identified issues and how you escalated them appropriately. This will illustrate your accountability and commitment to maintaining high standards.
