At a Glance
- Tasks: Conduct microbiological analysis and ensure product quality 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 personal and professional growth.
- Why this job: Be part of groundbreaking vaccine development and contribute to public health.
- Qualifications: Degree in Microbiology or relevant experience with GMP knowledge.
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 QC Micro team have a fantastic new opportunity to join the team here in Livingston, to undertake microbiological tasks and analysis for the release and monitoring of facilities, raw materials, intermediate and final product samples according to defined procedures and protocols, in accordance with regulatory requirements.
Responsibilities include:
- Perform Microbiological procedures including Total Viable Counts, Growth Promotion, Gram Stain, Microbial Growth Check by Incubation and Endotoxin for testing of raw materials, intermediate products and final product samples, according to defined SOPs and protocols.
- Perform In Operation & At Rest Environmental monitoring of Cleanrooms & Support areas as required, to support manufacturing processes and Facility Contamination Control (FCC).
- Comply with GMP guidelines and regulatory body requirements.
- Full compliance with HSE requirements.
- Write QMS documentation, e.g. SOPs, Deviations, Change Controls, CAPA.
- Maintain databases, logs and support the generation of QC trend data.
- Be responsible for QC Laboratories being clean, tidy and well-organised and in a state of continuous inspection readiness.
- Ability to work in a supportive and collaborative team setting and work individually as required. Shift work and out of hours work as required.
Your Experience ideally includes the following:
- Degree in Microbiology or related subject or relevant experience.
- Demonstrable experience working in a GMP environment.
- Good Aseptic Technique.
- Experience of Quality Management Systems.
Benefits:
- Stock Options.
- Employee Assistance Programme.
- Gym membership OR fitness allowance.
- EV Salary Sacrifice.
- Many others included.
QC Technician (Micro) in Livingston employer: Valneva
Valneva is an exceptional employer, particularly for those seeking a meaningful role in the healthcare sector. Located in Livingston, our inclusive and diverse work culture fosters collaboration and innovation, while offering robust employee growth opportunities through training and development. With benefits like stock options, gym memberships, and a supportive environment, we are dedicated to making a positive impact on global public health and ensuring our employees thrive both personally and professionally.
StudySmarter Expert Advice🤫
We think this is how you could land QC Technician (Micro) in Livingston
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Valneva. 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 Valneva.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Valneva. 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 Valneva is looking for. A tailored application can really make you stand out!
We think you need these skills to ace QC Technician (Micro) in Livingston
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 Valneva!
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 Valneva 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 Valneva!
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 Valneva, 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 Valneva
✨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 Valneva 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 Valneva’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.
