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Supervisor, Quality Assurance Operations

Supervisor, Quality Assurance Operations

ModernaGreat Barrington, MA, US
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Supervisor, Quality Assurance Operations

ModernaTX, Inc. seeks a Supervisor, Quality Assurance Operations for its Norwood, Massachusetts location.

Heres What Youll Do :

  • On behalf of a global biotechnology company, maintain responsibility for quality oversight of clinical operations.
  • Responsible for ensuring quality oversight of mRNA platform in clinical manufacturing.
  • Provide real-time quality leadership and on-the-floor operational support for the clinical manufacturing team.
  • Make quality decisions that may impact operations, ensuring appropriate escalation.
  • Coordinate training, professional development, and growth of the Clinical Quality Assurance team.
  • Monitor process operations to ensure compliance with procedures and specifications.
  • Demonstrate knowledge of standard manufacturing compliance, quality disposition, and quality system review.
  • Identify risks and communicate gaps for quality and GMP process / systems.
  • Enforce adherence to current Good Manufacturing Practices (cGMPs), standard operating procedures (SOPs), and manufacturing documentation.
  • Partner with manufacturing and support management teams to focus on site initiatives.
  • Oversee and perform review of executed electronic and paper batch record documentation.
  • Support product disposition.
  • Supervise approximately 4 Quality Assurance Operations Associates / Specialists.

Heres What Youll Bring to the Table :

Minimum requirements :

  • Requires a minimum of a Bachelors degree, or foreign equivalent, in Chemistry, Chemical Laboratory Technology, Manufacturing Engineering or a related field and 4 years of experience in the position offered, or as a Quality Assurance Specialist, Sr. Specialist, or related position.
  • Alternatively, employer will accept an Associates degree in the stated fields and 5 years of experience in the stated positions.
  • 4 years of experience must include :
  • Quality assurance in early and late-stage clinical products applying Good Manufacturing Practices (cGMP) and FDA guidelines;
  • Leveraging knowledge of Quality Management Systems (QMS) to review and approve deviations, change controls, and corrective and preventive actions (CAPAs);
  • Collecting, analyzing, and interpreting data related to quality metrics, defect rates, and process performance indicators; and
  • Performing risk assessments and implementing mitigation strategies.
  • May telecommute up to 2 days per week.
  • Apply at https : / / modernatx.wd1.myworkdayjobs.com / en-US / M_tx (Job ID : R17937) or email resume and cover letter to careers@modernatx.com with subject line : R17937.

    At Moderna, we believe that when you feel your best, you can do your best work. Thats why our US benefits and global well-being resources are designed to support youat work, at home, and everywhere in between.

  • Best-in-class healthcare coverage, plus a suite of voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Lifestyle Spending Accounts to personalize your well-being journey
  • Family planning and adoption benefits
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities
  • Location-specific perks and extras
  • 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.

    Our Working Model

    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.

    Moderna is a smoke-free, alcohol-free, and drug-free work environment.

    Equal Opportunities

    Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons 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 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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

    Accommodations

    Were 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 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 contact the Accommodations team at leavesandaccommodations@modernatx.com .

    Export Control Notice

    This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicants ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.

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