Associate II, Quality Control

The Role:

The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing. Also this individual may support special projects as assigned. This role is 1st or 2nd shift Monday to Friday (5 x 8hrs).

Heres What Youll Do:

• Requesting sampling releasing and shipping of raw materials

• Sample coordination including cross functional collaboration with internal and external labs

• Train and perform testing for methods including HPLC Bioanalyzer osmolality pH conductivity TruScan.

• RM spectroscopy appearance and dimensional verification.

• Supporting domestic and international sample shipments.

• Inspect product and raw material retain samples.

• LIMS (LabVantage) sample logging and result entry.

• AQL visual inspection of drug product.

• Raw material and consumable component inspection and release.

• Controlled temperature unit management maintenance and troubleshooting.

• Clean room gowning and aseptic techniques.

• Managing/stocking of QC lab supplies and routine lab cleaning.

• Write/revise SOPs protocols and reports.

• Complete and maintain cGMP documentation for work performed.

• Participate in initiating quality systems records such as deviations change controls CAPAs.

• Support investigations as required

• QC Management designee for QC inspection label issuance and reconciliation

• Establish and maintain a safe laboratory working environment.

• Foster a positive and inclusive work culture that promotes collaboration innovation and continuous improvement.

• Follow all relevant GxP regulations guidelines and company policies to ensure compliance with regulatory and internal requirements.

• Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions

• Follow Good Documentation Practices and Data Integrity requirements to ensure data documentation and records are completed and maintained for use by the business and available to support audits or inspections.

• Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence

Heres What Youll Need (Basic Qualifications):

• Education: BS in a relevant scientific discipline.

• Experience: 0-2 years with BS or 3 experience in GMP QC laboratory setting.

• Demonstrated aptitude or ability to learn: Able gain a strong understanding of GxP regulations.

Our Working Model

As we build our company we have always believed that an in-person culture is critical to our success. This role is 100% onsite reflecting the importance of being physically present to support the work collaborate closely with colleagues and contribute to our site-based operations.

Working onsite enables real-time collaboration strong team connections direct mentorship and the hands-on partnership needed to deliver our mission. 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.

Pay & Benefits

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

• Competitive healthcare plus voluntary benefit programs to support your unique needs
• A holistic approach to well-being with access to fitness mindfulness and mental health support
• Family planning benefits including fertility adoption and surrogacy support
• Generous paid time off including vacation volunteer days sabbatical global recharge days and a discretionary year-end shutdown
• Savings and investments to help you plan for the future
• Location-specific perks and extras

The salary range for this role is $63200.00 - $100900.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individuals position within the salary range will be based on several factors including but not limited to specific competencies relevant education qualifications certifications experience skills performance and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus other incentive compensation or equity award subject to company plan eligibility criteria and individual performance.

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.

If you want to make a difference and join a team that is changing the future of medicine we invite you to visit to learn more about our current opportunities.

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 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 .

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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