Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Join us in producing life-saving mRNA vaccines and operate cutting-edge production equipment.
- Company: Moderna, a leader in innovative vaccine production with a mission to make healthcare accessible.
- Benefits: Enjoy quality healthcare, generous paid time off, and wellness support.
- Why this job: Be part of a team making a real difference in global health.
- Qualifications: 3+ years in GMP manufacturing and a degree in Pharmaceutical production technology.
- Other info: Dynamic work environment with opportunities for growth and collaboration.
The predicted salary is between 30000 - 50000 £ per year.
Overview
Moderna is seeking a skilled Manufacturing Associate and digitally savvy Operator to join our mRNA vaccines production unit. The successful candidate will operate production equipment in accordance with cGMP compliance and health and safety regulations. The role requires excellent technical skills, a scientific approach, rapid learning capacity for new technologies in mRNA, and meticulousness. The position is central to Moderna’s mission of producing safe, effective vaccines and requires a balance of scientific understanding, operational skills, collaboration, and digital acumen.
Moderna’s mission includes establishing a leading-edge research, development, and manufacturing facility at Harwell as part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative aims to create highly skilled jobs and foster collaboration with academic, NHS, and government partners across the UK. We are seeking global experts to join us in this endeavor to help make life-saving vaccines accessible worldwide.
Responsibilities
- Adhering to Moderna’s safety procedures and maintaining housekeeping of assigned areas to ensure compliance and safety.
- Executing operations activities according to current good manufacturing practices (cGMP), standard operating procedures, and manufacturing documentation.
- Collaborating with QA peers for timely closure of documentation related to commercial batch disposition.
- Participating in investigations (RCA) and CAPA tasks to address deviations and compliance issues.
- Using performance tools in collaboration with the team to meet operational KPI objectives.
- Responding to and troubleshooting routine equipment, process, and digital issues rapidly.
Additional responsibilities
- Proactively identifying and reporting compliance or health and safety issues to supervisors.
- Keeping training records and documentation up to date.
- Performing routine maintenance tasks (e.g., lubrication, mechanical checks, filter changes) using hand tools.
- Flexibility to work off-hours and overtime when necessary.
- Contributing to multiple projects and continuous improvement initiatives in a fast-paced environment.
- Collaborating effectively in a dynamic, cross-functional matrix environment.
Requirements
- 3+ years of experience in a GMP manufacturing environment
- This site-based role requires presence at Moderna’s site full-time and is not eligible for remote work
Qualifications & Skills
- A university degree with a specialization in Pharmaceutical production technology or equivalent
- Experience with filtration and chromatography, and cold chain management a plus
- Experience in audit/inspection preparation, understanding Health authority and regulatory guidelines
- Ability to collaborate fluidly with peers, leadership and cross-functional support groups
- Excellent written, oral communication, and organizational skills
- Ability to maintain attention to detail while executing multiple tasks with minimal supervision
- Demonstrated commitment to Moderna\’s values of Bold, Collaborative, Curious, and Relentless
Benefits
- Quality healthcare and insurance benefits
- Lifestyle Spending Accounts to support well-being
- Free premium access to fitness, nutrition, and mindfulness classes
- Family planning and adoption benefits
- Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown
- Savings and investments
- Location-specific perks and extras
Work Model & Hours
Moderna’s working hours and shift patterns are under review for 24/7 operations. The 2-2-3 Panama schedule describes a 28-day rotation with 12-hour shifts, typically involving four teams with cycles of work and rest days. Outside of campaign periods, shifts may revert to a standard Monday to Friday model.
Moderna is a smoke-free, alcohol-free, and drug-free work environment. Moderna is committed to equal opportunity in employment and non-discrimination for all applicants, and to offering reasonable accommodations where needed. For accommodations, contact the Accommodations and Adjustments team at leavesandaccommodations@modernatx.com.
To learn more about current opportunities, visit modernatx.com/careers
#J-18808-Ljbffr
(Fixed-Term) Manufacturing Associate II - Shift Position employer: Moderna
Contact Detail:
Moderna Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land (Fixed-Term) Manufacturing Associate II - Shift Position
✨Tip Number 1
Get to know the company inside out! Research Moderna's mission, values, and recent projects. This will help you tailor your conversations and show that you're genuinely interested in being part of their team.
✨Tip Number 2
Network like a pro! Connect with current employees on LinkedIn or attend industry events. Building relationships can give you insider info and might even lead to a referral, which is always a bonus!
✨Tip Number 3
Prepare for the interview by practising common questions related to GMP and mRNA technologies. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your relevant experience.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the Moderna team and ready to contribute to their mission.
We think you need these skills to ace (Fixed-Term) Manufacturing Associate II - Shift Position
Some tips for your application 🫡
Show Off Your Skills: Make sure to highlight your technical skills and experience in GMP manufacturing. We want to see how your background aligns with the role, so don’t hold back on showcasing your expertise!
Tailor Your Application: Take a moment to customise your application for this specific role. Use keywords from the job description to demonstrate that you understand what we’re looking for and how you fit into our mission.
Be Clear and Concise: When writing your application, keep it clear and to the point. We appreciate well-structured responses that get straight to the heart of your qualifications and experiences.
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 this exciting opportunity at Moderna.
How to prepare for a job interview at Moderna
✨Know Your GMP Basics
Make sure you brush up on your knowledge of current Good Manufacturing Practices (cGMP). Be ready to discuss how you've applied these principles in your previous roles, as this will show your understanding of the industry's standards and your commitment to safety.
✨Show Off Your Technical Skills
Prepare to talk about your experience with production equipment and any specific technologies related to mRNA vaccines. Highlight any hands-on experience you have with filtration, chromatography, or cold chain management, as these are key areas for the role.
✨Collaboration is Key
Since the role involves working closely with QA and other teams, think of examples where you've successfully collaborated in a cross-functional environment. Be ready to share how you handle communication and teamwork, especially when troubleshooting issues.
✨Be Ready for Rapid Learning
Demonstrate your ability to learn quickly by discussing instances where you've had to adapt to new technologies or processes. This will show that you're not just technically skilled but also curious and eager to grow within the role.
