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    Production Supervisor Nightshift - Oxford, Oxfordshire, United Kingdom - Moderna Therapeutics

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    Description
    Manufacturing Supervisor, Drug Substance, Night Shift page is loaded Manufacturing Supervisor, Drug Substance, Night Shift
    Apply locations Oxford - England Drug Manufacturing time type Full time posted on Posted 2 Days Ago job requisition id R15088 *We are excited to announce that we are expanding our team and have multiple positions available for this role - join us in shaping the future
    • 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.

    Our mission is to establish a leading-edge research, development, and manufacturing facility, 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 and NHS partners across the UK.

    Moderna is seeking a Night Shift Manufacturing Supervisor, Drug Substance for our state-of-the-art mRNA vaccines production unit at our Manufacturing Site in the UK.

    This role is pivotal in managing production timelines, ensuring cGMP compliance, and overseeing health and safety regulations.

    You will be instrumental in the technical ramp-up of manufacturing processes and be required to demonstrate digital proficiency and operational leadership.

    Enforce safety procedures and Moderna's guidelines, ensuring compliance with local HSE requirements.
    Start fostering a collaborative relationship with the Day Shift team.
    Develop batch records, SOPs, and training materials for various phases of commercial programs.
    Coordinate with the Quality Assurance team for the timely disposition of commercial batches.
    Manage documentation processes and oversee training and development of staff.
    Manage team performance and development, including regular one-on-one sessions.
    Collaborate with Supply Chain to maintain inventory and review process orders.
    Respond to routine equipment, process, and digital issues, ensuring continuous operation.
    Lead projects aimed at continuous improvement, aligning operations with corporate goals and commercial demand.
    Drive initiatives to maintain manufacturing excellence.
    Ensure team performance monitoring and make necessary adjustments for improvement.
    Lead in troubleshooting and optimizing manufacturing processes.
    Typically, 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
    Proven track record of success in a fast-paced production environment at a biotech/pharmaceutical company preferably in GMP
    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
    Experience in coordinating with supply chain for raw materials and inventory management.
    We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
    Quality healthcare and insurance benefits
    Lifestyle Spending Accounts to create your own pathway to well-being
    Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown

    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.If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.

    Moderna is committed to equal employment opportunity 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.

    Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
    Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities.

    Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at .

    Team Lead - mRNA Vaccines Production – Night Shift
    locations 2 Locations time type Full time posted on Posted 3 Days Ago Manufacturing Supervisor, Drug Product - Night Shift
    locations 2 Locations time type Full time posted on Posted 2 Days Ago Manufacturing Supervisor, Drug Substance - Day Shift
    locations 2 Locations time type Full time posted on Posted 2 Days Ago #J-18808-Ljbffr


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