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Senior Manager, Analytical Science & Technology; AS&T

Job in Norwood, Jefferson County, Kentucky, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-02
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 130800 - 209400 USD Yearly USD 130800.00 209400.00 YEAR
Job Description & How to Apply Below
Position: Senior Manager, Analytical Science & Technology (AS&T)
Location: Norwood

The Role

Moderna is seeking a Senior Manager – Analytical Sciences & Technology (AS&T) – CMC based at their Norwood, MA site. The Senior Manager, AS&T - CMC Lead will provide technical expertise and program support for analytical method related activities that support late‑phase development and commercial programs. This individual contributor role will oversee qualification, validation, transfer, and lifecycle strategies for analytical methods across a global network.

The ideal candidate will have a strong background in regulatory submissions, analytical sciences, and method validation, with proven experience in late‑stage and commercial product support.

What You’ll Do
  • Late-Phase & Commercial Program Strategy
  • Method Transfer Leadership
  • Validation Master Plan Ownership
  • Analytical Method Lifecycle Management
  • Regulatory Submission Support
  • Regulatory Commitments & Queries
What You’ll Need (Basic Qualifications)
  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field
  • 8+ years of experience in Analytical Development, Quality Control, or related functions within the biopharmaceutical industry.
  • Strong expertise in analytical method qualification, validation, and lifecycle management in late‑phase and commercial settings.
  • Proven experience with regulatory submissions (BLA, MAA, etc.) and direct interactions with global health authorities.
  • In‑depth knowledge of ICH guidelines, GMP regulations, and industry best practices.
  • Excellent technical writing skills and ability to author high‑quality regulatory documentation.
  • Strong collaboration, communication, and influencing skills across cross‑functional and global teams.
  • This position is site‑based, requiring you to be at Moderna’s site full‑time. This position is not eligible for remote work.
What You’ll Bring to the Table (Preferred Qualifications)
  • Advanced degree (M.S., Ph.D.) in a scientific discipline.
  • Experience supporting biologics, vaccines, or other complex modalities.
  • Prior experience in global method transfers and managing a network of manufacturing/testing sites.
Work Environment & Expectations
  • This is an individual contributor position with high visibility and strategic impact.
  • Role requires cross‑functional engagement with Regulatory Affairs, Quality Control, Manufacturing and Technical Operations.
  • Some domestic and international travel may be required to support site transfers and regulatory engagements.
Pay & Benefits

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

  • Best‑in‑class healthcare coverage, 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 investment opportunities to help you plan for the future
  • Location‑specific perks and extras

The salary range for this role is $ - $. 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 individual’s 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.

Equal Opportunities

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…

Position Requirements
10+ Years work experience
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