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- Tasks: Supervise manufacturing processes and ensure compliance with quality standards.
- Company: Join a leading vaccine company making a global health impact.
- Benefits: Enjoy stock options, gym memberships, and professional development opportunities.
- Why this job: Be part of a diverse team dedicated to innovative vaccine production.
- Qualifications: Degree in a relevant field and 3+ years of supervisory experience required.
- Other info: Flexible schedules and a positive team environment await you!
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 that is open to people of all backgrounds. Our diverse and inclusive workforce makes Valneva a great place to work.
Our specialist manufacturing team is looking to recruit an experienced supervisor to join the team. The purpose of this role is to coordinate the execution of manufacturing steps according to defined procedures and protocols in line with cGMP work practices and quality standards. This role is dedicated to supervising production and resources, reviewing, organizing, and developing systems/processes to achieve:
- Effective supervisory control of all production activities
- Effective management of a small team of manufacturing staff
- Effective planning and coordination of manufacturing activities
- Effective planning and coordination with support functions
Responsibilities include:
- Planning and coordinating production plans to deliver products on time, with quality and cost considerations
- Ensuring all production steps are executed in compliance with cGMP standards
- Preparing manufacturing rooms for activities, ensuring availability of materials and documentation
- Supervising activities in cleanrooms
- Ensuring team and visitor safety, investigating safety events, and tracking actions
- Completing and maintaining accurate documentation for manufacturing activities
- Applying best cGMP practices and ensuring equipment, facilities, and materials meet standards
- Training and ensuring staff competency and compliance
- Managing cell bank activities, FBS qualification, and virus seedbank manufacture
- Motivating staff, reporting issues, and executing training plans
- Developing and reporting on quality and business metrics for continuous improvement
- Identifying process improvement opportunities
- Managing deviations, change controls, and CAPAs
- Maintaining a clean, organized, and inspection-ready environment
- Conducting activities safely and in compliance with HSE requirements
- Fostering a positive team environment and participating in improvement initiatives
- Managing team absence and performance reviews
- Performing other duties as required by management
Experience:
- Degree or equivalent experience in a relevant field
- At least 3 years of senior production experience
- Proven supervisory experience of 4+ staff
- Experience in vaccine production and animal cell culture
- Cell bank experience
Required Skills:
- Flexibility for varying schedules (shift/weekend)
- Understanding of the pharmaceutical industry
- Professional attitude and confidence in staff management
- Ability to develop team culture and recognize staff behaviours
Benefits include stock options, employee assistance, gym membership or fitness allowance, LinkedIn Learning, among others.
Manufacturing Supervisor – Livingston, United Kingdom employer: Valneva SE
Contact Detail:
Valneva SE Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manufacturing Supervisor – Livingston, United Kingdom
✨Tip Number 1
Familiarise yourself with cGMP standards and practices, as this role heavily emphasises compliance. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to quality and safety in manufacturing.
✨Tip Number 2
Highlight any experience you have in vaccine production or animal cell culture during networking opportunities. Engaging with professionals in the field can provide insights and potentially lead to referrals that could strengthen your application.
✨Tip Number 3
Showcase your leadership skills by discussing specific examples of how you've motivated teams or improved processes in previous roles. This will resonate well with the hiring managers looking for someone who can effectively manage a small team.
✨Tip Number 4
Research the company’s recent developments and their impact on global public health. Being knowledgeable about their products and initiatives will allow you to engage in meaningful conversations during interviews, showing your genuine interest in the role.
We think you need these skills to ace Manufacturing Supervisor – Livingston, United Kingdom
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in manufacturing and supervisory roles. Emphasise any specific experience you have in vaccine production or working under cGMP standards.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for public health and your understanding of the pharmaceutical industry. Mention how your skills align with the responsibilities outlined in the job description.
Highlight Relevant Skills: In your application, focus on key skills such as team management, planning and coordination, and process improvement. Provide examples of how you've successfully applied these skills in previous roles.
Proofread Your Application: Before submitting, carefully proofread your application to eliminate any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a manufacturing environment.
How to prepare for a job interview at Valneva SE
✨Know Your cGMP Standards
Familiarise yourself with current Good Manufacturing Practices (cGMP) as they are crucial in the pharmaceutical industry. Be prepared to discuss how you have applied these standards in your previous roles, especially in relation to vaccine production.
✨Demonstrate Leadership Skills
As a Manufacturing Supervisor, you'll need to manage a team effectively. Share examples of how you've motivated staff, handled conflicts, or improved team dynamics in past positions. Highlight your ability to foster a positive team environment.
✨Showcase Problem-Solving Abilities
Be ready to discuss specific instances where you've identified process improvements or managed deviations and change controls. This will demonstrate your proactive approach to maintaining quality and efficiency in manufacturing.
✨Prepare for Safety Discussions
Safety is paramount in manufacturing environments. Prepare to talk about your experience with safety protocols, investigating safety events, and ensuring compliance with HSE requirements. This shows your commitment to a safe working environment.