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Manufacturing supervisor, drug substance - shift position

Harwell (DN10 5)
Manufacturing supervisor
Posted: 8 May
Offer description

The Role Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.​ Moderna's mission is to establish 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 will create a multitude of highly skilled jobs and foster collaboration with academic, NHS, and government partners across the UK. We're looking for global experts eager to join us in this endeavor, contributing to a future where access to life-saving vaccines is a reality for all.​ As a Team Lead in Manufacturing Operations, you will play a pivotal role in ensuring that Moderna’s production timelines and operational efficiencies align with the highest industry standards. You will lead a team responsible for executing cGMP-compliant manufacturing processes, overseeing health and safety adherence, and driving digital excellence in production workflows. Your expertise will contribute directly to the production of safe, effective mRNA vaccines, supporting our mission to revolutionize medicine. This role requires a blend of technical proficiency, operational leadership, and strong people management skills. The ideal candidate will foster a culture of excellence, mentor manufacturing associates, and champion a digital-first mindset to enhance team coordination and manufacturing efficiency. Here’s What You’ll Do Your key responsibilities will be: Lead a team responsible for executing cGMP-compliant manufacturing operations, ensuring adherence to health, safety, and environmental (HSE) regulations. Oversee the technical ramp-up of manufacturing processes and remain informed about advancements in mRNA technology. Maintain performance monitoring using established KPIs, ensuring production plans meet corporate goals and commercial demand. Act as a mentor and trainer, developing and retaining manufacturing associates to sustain a high-performing team. Manage team performance, including recognition, succession planning, and addressing performance gaps through structured feedback. Support supply chain management by overseeing inventory levels, process orders, and ensuring timely commercial batch disposition. Lead and participate in cross-functional projects focused on continuous improvement and operational efficiency. Your responsibilities will also include: Ensure full compliance with Moderna’s safety procedures, reinforcing gowning protocols and maintaining a clean general operating area. Open and investigate incidents, deviations, and HSE events in coordination with cross-functional teams. Develop batch records, SOPs, and training materials to support manufacturing processes. Collaborate closely with QA peers to ensure seamless documentation and timely batch disposition. Troubleshoot routine equipment, process, and digital issues to minimize disruptions. Adapt to off-hour work requirements, including overtime, as needed to support commercial demand. Align production schedules with corporate objectives, identifying risks and mitigating potential workflow disruptions. The key Moderna Mindsets you’ll need to succeed in the role: We behave like owners – You will lead your team with accountability and commitment, ensuring seamless manufacturing execution and continuous improvement of processes that go beyond any job description. You will take initiative, make data-driven decisions, and inspire those around you to take pride in Moderna’s mission. We digitize everywhere possible – You will leverage digital tools to enhance manufacturing efficiency, streamline team coordination, and optimize operational performance. Your ability to embrace digital-first solutions will be critical in maximizing our impact on patients. Here’s What You’ll Need ( Basic Qualifications) 5-7 years of experience in a GMP manufacturing environment A bachelor's degree in biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or related field preferred This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. Here’s What You’ll Bring to the Table (Preferred Qualifications) Proven track record of success in a fast-paced production environment at a biotech/pharmaceutical company preferably in GMP Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless, embodying these values in the workplace Ability to collaborate fluidly with peers, supervisors and cross-functional support groups required Exceptional written, oral communication, and organizational skills required Skills in project management, including planning, execution, monitoring, and closing projects. Experience with chromatography and tangential flow filtration would be an asset Experience in audit / inspection preparation, understanding Health authority and regulatory guidelines Knowledge of environmental monitoring practices in a cleanroom or controlled manufacturing environment Specific expertise in mRNA technology, vaccine production and equipment - beyond a general scientific understanding Understanding/Detailed knowledge of regulatory requirements specific to mRNA drug products and vaccine production Expertise in quality control measures and assurance processes specific to pharmaceutical manufacturing Knowledge of validation processes for manufacturing equipment and processes Ability to analyze production data and generate reports for management Specific methodologies for continuous improvement, such as Lean, Six Sigma, or others. Experience in leading Kaizen events or other process optimization initiatives Experience in coordinating with supply chain for raw materials and inventory management. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. At Moderna, we believe that when you feel your best, you can do your best work. That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between. Quality healthcare and insurance benefits Lifestyle Spending Accounts to create your own pathway to 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 a discretionary year-end shutdown Savings and investments Location-specific perks and extras! The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at leavesandaccommodations@modernatx.com. LI-JP1 -

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