MSAT CDMO Manager
Listed on 2026-08-03
-
Pharmaceutical
Regulatory Compliance Specialist, Validation Engineer
Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and United Kingdom, Lantheus has been providing radiopharmaceutical solutions for nearly 70 years.
Today, we’re expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world.
At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We’re dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress.
Join us and be part of a company where your contributions make a real impact, because we know someone’s health is in our hands.
Summary of role
We are seeking a Manager of CDMO Manufacturing Science & Technology (MSAT) for our Springfield location. The MSAT CDMO Manager provides technical and people leadership for MSAT activities supporting pharmaceutical and/or radiopharmaceutical drug product manufacturing across internal and external manufacturing networks. This role is accountable for execution of multiple technology transfer and manufacturing support projects while ensuring alignment with cGMP requirements and business objectives.
The MSAT CDMO Manager leads MSAT staff, interfaces with senior stakeholders, and ensures delivery of technically sound and compliant manufacturing solutions.
This position is based in New Jersey and requires a presence on-site 5 days per week, and open to applicants authorized to work for any employer within the United States.
Responsibilities
- Lead multiple MSAT projects, including full technology transfer execution from initiation through commercial manufacturing.
- Lead and manage team staff, including assignment of work, prioritization of activities, mentoring, and technical development of team members.
- Serve as primary MSAT technical lead for assigned manufacturing sites and external partners.
- Oversee and approve deviation investigations, CAPAs, and change controls.
- Provide technical oversight for process validation, qualification, and lifecycle management activities.
- Review and approve technical documentation including tech transfer packages, validation strategies, and regulatory support documents.
- Provide strategic input into control strategies, process robustness, and continuous improvement initiatives.
- Lead, mentor, and develop MSAT scientists; assign work and manage priorities.
- Collaborate with Quality, Manufacturing, Validation, Supply Chain, and Regulatory Affairs to ensure aligned execution.
- Represent MSAT during regulatory inspections, audits, and governance forums.
- Actively promote safety culture and Lantheus values.
Basic Qualifications
- Bachelor’s degree with 7+ years of relevant experience;
Master’s degree with 5+ years; or PhD with 3+ years of relevant experience. - Demonstrated experience leading tech transfer and manufacturing support activities in a regulated environment.
- Prior experience managing or leading technical teams.
- Strong understanding of cGMPs and regulatory expectations.
Other Requirements
- Willingness to work onsite and travel up to ~20% as required.
- Strong leadership, communication, and decision‑making skills.
- Ability to manage multiple complex technical initiatives concurrently.
- Strong organizational, communication, and problem-solving skills.
- Experience with radiopharmaceuticals is preferred.
- Understanding GMP/GLP principles.
- Knowledge of hazardous material safety and cGMP requirements.
- Strong attention to detail and documentation accuracy
- Previous lab experience in Manufacturing and/or Quality Control at an aseptic processing facility is preferred.
- Previous experience in Quality, Compliance and/or Manufacturing of radiopharmaceutical products is preferred.
Core Values
The ideal candidate will embody Lantheus core values:
- Let people be their best
- Resp…
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).