Manager, QC Stability

5 days ago


Norwood, United States Moderna, Inc. Full time

The Role

In this role, you will assist in managing operational oversight of the stability programs within the Norwood Quality Control team. You will be responsible for leading and overseeing all operational aspects of the in-house stability program, focusing on the commercial stability program. You will interact closely with partners within Global Stability, Technical Development, Digital Lab Systems, QC laboratories, and more.

Heres What Youll Do

Lead the day-to-day operations of the Norwood QC stability program including and not limited to stability study initiations, pull and set down schedules, stability protocols, program metrics, stability data reporting and trending, stability assessments for investigations, change controls and other quality systems as required.

Responsible for management of stability data using LIMS system and other digital tools as required; compilation of reports and trending for both internal and external reporting purposes such as expiry evaluations, OOS/OOT investigations, regulatory filings, regulatory commitments, and annual product quality reports.

Author, review, revise and approve various documentation related to stability program operation including stability protocols, reports, specifications, SOPs, expiry and shelf-life assessments.

Track, monitor and report on stability program metrics and KPIs; effectively utilize metrics and KPIs to identify areas for continuous improvement and implement corrective or preventative action plans.

Support various quality systems as related to the stability program including deviations, OOS/OOT investigations, change controls, CAPAs and effectiveness checks ensuring on-time record metrics achieved.

Collaborate closely with program teams to consistently meet timelines for availability of critical stability data needed to support filings and regulatory agency commitments.

Partner with Norwood QC lab teams to drive on-time testing and review of stability samples.

Serve as QC stability program subject matter expert for health authority inspections as well as team guidance and mentorship.

May lead or support internal or cross functional projects related to the stability program.

Additional duties as may be assigned from time to time

Heres What Youll Need (Basic Qualifications)

Advanced degree in a scientific discipline (e.g., Biology, Chemistry, Pharmacy) or related field.

BS with 5-8 years, MS with 3-5 years in cGMP Quality Control environment or similar pharmaceutical quality discipline.

Heres What Youll Bring to the Table (Preferred Qualifications)

Working knowledge of GMP regulations, ICH guidelines, and stability testing requirements.

Extensive experience with stability programs and ideally supporting commercial stability.

Excellent organizational, communication, and problem-solving skills.

Ability to work effectively in a fast-paced, dynamic environment.

Experience with regulatory inspections and interactions with health authorities.

A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:

Highly competitive and inclusive medical, dental and vision coverage optionsFlexible Spending Accounts for medical expenses and dependent care expensesLifestyle Spending Account funds to help you engage in personal enrichment and self-care activitiesFamily care benefits, including subsidized back-up care options and on-demand tutoringFree premium access to fitness, nutrition, and mindfulness classesExclusive preferred pricing on Peloton fitness equipmentAdoption and family-planning benefitsDedicated care coordination support for our LGBTQ+ communityGenerous paid time off, including:
Vacation, sick time and holidays
Volunteer time to participate within your community
Discretionary year-end shutdown
Paid sabbatical after 5 years; every 3 years thereafterGenerous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents 401k match and Financial Planning toolsModerna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit optionsComplimentary concierge service including home services research, travel booking, and entertainment requestsFree parking or subsidized commuter passesLocation-specific perks and extras

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, theinfrastructure 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 peopleare 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 proud to be an equal opportunity workplace and is an affirmative action employer.

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. Were focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to 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. (EEO/AAP Employer)

-



  • Norwood, Massachusetts, United States Moderna, Inc. Full time

    The Role: The Senior Manager will manage operational oversight of the clinical and commercial stability programs within the Norwood Quality Control team. He/she/they will be responsible for leading and overseeing all technical and operational aspects of the in-house stability program for clinical and commercial products. The Senior Manager will interact...

  • Manager, QC Chemistry

    3 months ago


    Norwood, United States Moderna, Inc. Full time

    The RoleModerna is seeking a Manager, Chemistry to support our Quality Control team specializing in Individualized Neoantigen Therapy (INT) clinical production. This position will be based in our cGMP Manufacturing site in Norwood, MA. The individual in this role will focus on managing QC Analysts and supervisors in support of Analytical activities including...


  • Norwood, United States Moderna, Inc. Full time

    The Role: This individual contributor role involves leading the global implementation and maintenance of laboratory automation and robotics across Modernas Quality Control (QC) laboratories. The incumbent will be responsible for the project planning, coordinating implementation, and management of automated systems including Hamilton liquid handlers, Andrew+...


  • Norwood, Massachusetts, United States Moderna, Inc. Full time

    The Role: This individual contributor role involves leading the global implementation and maintenance of laboratory automation and robotics across Modernas Quality Control (QC) laboratories. The incumbent will be responsible for the project planning, coordinating implementation, and management of automated systems including Hamilton liquid handlers, Andrew+...


  • Norwood, United States Randstad Life Sciences Full time

    Job DescriptionJob Description6 Month ContractNorwood, MAPR: $27-32/hour SHIFT: 3/2/2/3/2/2 schedule 12-hour rotating day shift, 6am – 6pmOR12-hour rotating day shift, 6pm – 6am Job SummaryIn this role, you will perform routine sample management and support various laboratory activities at Moderna’s manufacturing facility. This position will focus...


  • Norwood, United States Randstad Life Sciences Full time

    Job DescriptionJob Description6 Month ContractNorwood, MAPR: $25-34/hourShift: M-F, 2nd Shift Job SummaryReporting to the Supervisor of Quality Control, Seeking a Quality Control Raw Materials Associate I, Sampler based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further...


  • Norwood, Massachusetts, United States Randstad Full time

    Job Summary:As a leading staffing and recruitment agency, Randstad is committed to finding top talent for prestigious life sciences and biopharma companies. We offer a unique opportunity for individuals to grow and learn in a dynamic environment.Key Responsibilities:Perform cGMP QC Chemistry testing for QC Chemistry, release, stability, and in-process...


  • Norwood, Massachusetts, United States Randstad Full time

    Job Summary:As a leading staffing and recruitment agency, Randstad is committed to finding top talent for prestigious life sciences and biopharma companies. We offer a unique opportunity for individuals to grow and learn in a dynamic environment. Our extensive network of top employers and detailed information about hundreds of positions make us the ideal...


  • Norwood, United States Randstad Life Sciences Full time $30 - $38

    Job DescriptionJob DescriptionAn immediate need for a A major Pharmaceutical company whose mission is to deliver the greatest possible impact to people through innovative medicines. Join this team to make a world of Change!2nd Shift, WED-SATJob SummaryIn this role, you will perform cGMP QC Chemistry testing for QC Chemistry, release, stability and in process...


  • Norwood, Massachusetts, United States Randstad Full time

    Job Summary: As a leading staffing and recruitment agency, Randstad is committed to finding top talent for life sciences and biopharma companies. Our extensive network and detailed information about hundreds of positions make us the ideal partner for your job search. If you're looking for a role where you can make a difference in others' lives, we have the...

  • Quality Control

    6 days ago


    Norwood, United States Randstad Life Sciences US Full time

    Associate II, Quality Control - Sample Management6 MonthsNorwood, MAHourly Pay: $38.75SHIFT: 3/2/2/3/2/2 schedule (12-hour rotating night shift, 3pm – 3am)Job SummaryIn this role, you will perform routine sample management and support various laboratory activities at manufacturing facility. This position will focus on general lab support activities. The...

  • Quality Control

    5 days ago


    Norwood, United States Randstad Life Sciences US Full time

    Associate II, Quality Control - Sample Management6 MonthsNorwood, MAHourly Pay: $38.75SHIFT: 3/2/2/3/2/2 schedule (12-hour rotating night shift, 3pm – 3am)Job SummaryIn this role, you will perform routine sample management and support various laboratory activities at manufacturing facility. This position will focus on general lab support activities. The...

  • Food Safety Manager

    9 hours ago


    Norwood, New Jersey, United States Winpak Full time

    Job SummaryWe are seeking a highly motivated and experienced Food Safety Manager to join our team at Winpak. The successful candidate will be responsible for leading the development and implementation of our SQF Certified System, ensuring the effectiveness of the system through verification, validation, and ongoing maintenance.Key ResponsibilitiesDevelop and...


  • Norwood, United States Activate Care Full time

    Job DescriptionJob Description** This is an onsite role where applicants should reside within the Norwood, MA area to be considered for this position. **About Activate Care:At Activate Care, we’re on a mission to improve health equity and drive improved health outcomes across the country. Our Community Care Record platform enables healthcare and community...


  • Norwood, Massachusetts, United States Randstad Life Sciences US Full time

    Contract PositionLocation: Norwood, MAPay Rate: $30-38/hour Available Shifts: Sunday to Wednesday, Day Shift: 8:00 AM - 6:00 PMORWednesday to Saturday, Evening Shift: 2:00 PM - 12:00 AMORSunday to Wednesday, Night Shift: 10:00 PM - 8:00 AMORWednesday to Saturday, Night Shift: 10:00 PM - 8:00 AM In this position, you will conduct cGMP Quality Control...


  • Norwood, Massachusetts, United States Actalent Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Equipment Specialist to join our team at Actalent. As a Quality Assurance Equipment Specialist, you will be responsible for ensuring the quality and reliability of our equipment and systems.Key ResponsibilitiesEquipment Maintenance and Troubleshooting: Support the team in investigating and...


  • Norwood, Massachusetts, United States Actalent Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Equipment Specialist to join our team at Actalent. As a Quality Assurance Equipment Specialist, you will play a critical role in ensuring the quality and reliability of our equipment and systems.Key ResponsibilitiesEquipment Maintenance and Troubleshooting: Support the team in investigating and...


  • Norwood, Massachusetts, United States Randstad Full time

    Job Overview: At Randstad, the leading staffing and recruitment agency globally, we are dedicated to connecting you with the ideal opportunity that fosters your growth in the life sciences sector. By leveraging our extensive network of esteemed employers, we provide you with insights into numerous positions that align with your career aspirations. If you are...


  • Norwood, United States firstPRO, Inc Full time

    firstPRO is now accepting resumes for an LMS Technical Project Manager in Norwood, MA. This is a direct hire role and onsite 2 days per week.The Labvantage LIMS Sr. Technical Project Manager will report to and work closely with the Director, Digital LIMS Systems to ensure the implementation of new solutions and improvement of existing systems (LabVantage)...


  • Norwood, United States firstPRO, Inc Full time

    firstPRO is now accepting resumes for an LMS Technical Project Manager in Norwood, MA. This is a direct hire role and onsite 2 days per week.The Labvantage LIMS Sr. Technical Project Manager will report to and work closely with the Director, Digital LIMS Systems to ensure the implementation of new solutions and improvement of existing systems (LabVantage)...