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- Tasks: Supervise microbiological tests and ensure quality control in a dynamic lab environment.
- Company: Join a leading vaccine company making a global health impact.
- Benefits: Enjoy stock options, gym membership, and an employee assistance programme.
- Why this job: Be part of groundbreaking vaccine development and contribute to public health.
- Qualifications: Experience in QC labs, GMP knowledge, and strong leadership skills required.
- Other info: Collaborative team culture with opportunities for continuous improvement and career growth.
The predicted salary is between 36000 - 60000 £ 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.
We are seeking a skilled and versatile Senior QC Technician (Micro) to join our team. To supervise and perform Microbiological tests for the release of raw materials and intermediate products according to defined procedures and protocols. Provide technical expertise in Microbiological assays and drive projects to completion to agreed timelines. Oversee the daily running of the laboratories and support the Microbiology Manager.
Responsibilities
- Execute Microbiological procedures including Endotoxin Kinetic Chromogenic Method, Total Viable Count Testing, Growth Promotion including Environmental Isolates, Microbial Growth Check by Incubation, Environmental Monitoring including Gowning and Compressed Gases, and any other testing as required by the Line Manager.
- Apply cGMP work-practices and techniques to test and release raw materials and intermediate products.
- Ensure that all QC technicians are appropriately trained and competent in the procedures they are conducting and are following cGMP working practices at all times.
- Ensure appropriate trending is up to date to allow the reporting of the rolling monthly environmental monitoring report in a timely manner.
- Be responsible for the development, collating and reporting of key quality and business metrics, and use such metrics to drive a culture of continuous process improvement within the area of responsibility.
- Conduct on-time reporting according to the defined and trained document management standards including review and verification of microbiological data provided by the QC technicians.
- Immediately escalate and report any deviations to materials, facilities, processes, or procedures to the Manager.
- Be accountable for the microbiological laboratories being clean, tidy, and well organised and in a state of continuous inspection readiness.
- Write QMS documentation including SOPs, Change Control, Deviations, CAPAs.
- Identify areas for continuous improvement and escalate those to the Microbiological Manager and QC Head of Department.
- Actively contribute to the development and maintenance of an enthusiastic, supportive, and collaborative environment within the team-setting.
- To undertake any other duties as requested by the line manager in accordance with company requirements.
- Shift work and out of hours work as required.
Experience
- Working within a QC laboratory environment, working to GMP within a recognised quality system.
- Experience of working in a Supervisor/Senior role.
- Ability to prioritise, organise and schedule work within a busy laboratory.
- Experience of writing and working to SOP documentation.
- QMS experience in writing Deviations, CAPAs, Change Control.
- Experience in Environmental Monitoring.
- Technical experience and understanding in Microbiological assays such as Sterility, Endotoxin, Mycobacteria & Mycoplasma.
- Understanding of the European and U.S. Pharmacopeia desirable.
- Validation and qualification of assays knowledge would be advantageous.
- Experience driving a team to achieve individual, team and organisational objectives.
- Experienced in relationship handling with external bodies, such as suppliers, regulatory and audit authorities.
Benefits
- Stock Options
- Employee Assistance Programme
- Gym membership OR fitness allowance
- EV Salary Sacrifice
- Many others included
Senior QC Technician (Micro) in Livingston employer: Seleville Business Solutions
Contact Detail:
Seleville Business Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QC Technician (Micro) in Livingston
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work in QC or microbiology. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Make sure you can confidently discuss microbiological assays and cGMP practices. We want you to shine when it comes to showcasing your expertise!
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in the interviewer's mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, you’ll be part of a diverse and inclusive team that’s making a real impact on global public health.
We think you need these skills to ace Senior QC Technician (Micro) in Livingston
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior QC Technician role. Highlight your experience in microbiological testing and any relevant supervisory roles. We want to see how your skills match what we're looking for!
Showcase Your Experience: In your cover letter, don’t just list your qualifications; tell us about specific projects or achievements that demonstrate your expertise in cGMP practices and microbiological assays. We love a good story!
Be Clear and Concise: When writing your application, keep it clear and to the point. Use bullet points where possible to make it easy for us to read through your qualifications and experiences. We appreciate 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. We can’t wait to hear from you!
How to prepare for a job interview at Seleville Business Solutions
✨Know Your Microbiology Inside Out
Make sure you brush up on your microbiological assays and cGMP practices. Be ready to discuss specific techniques like Endotoxin Kinetic Chromogenic Method and Total Viable Count Testing. Showing that you can talk confidently about these methods will impress the interviewers.
✨Showcase Your Leadership Skills
As a Senior QC Technician, you'll be supervising others. Prepare examples of how you've led teams in the past, especially in a QC lab environment. Highlight any experience you have in training staff or driving projects to completion.
✨Be Ready for Problem-Solving Questions
Expect questions about how you would handle deviations or issues in the lab. Think of scenarios where you identified areas for improvement or dealt with unexpected challenges. This will demonstrate your critical thinking and proactive approach.
✨Understand the Company’s Impact
Familiarise yourself with the company’s mission and the vaccines they develop. Being able to articulate why you want to work for a company that addresses unmet medical needs will show your passion and alignment with their goals.
