Lantheus Holdings

MSAT CDMO Manager

Lantheus Holdings$111K — $185K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 7+ years of experience; Master's degree with 5+ years; or PhD with 3+ years of experience in a relevant field.
  • Experience in leading technology transfer and manufacturing support in a regulated environment.
  • Proven ability in managing or leading technical teams.
  • In-depth knowledge of cGMP regulations and expectations.

Responsibilities

  • Lead multiple MSAT projects from technology transfer initiation through to commercial manufacturing.
  • Manage and mentor MSAT team, prioritizing assignments and developing team skills.
  • Act as the primary technical lead for assigned manufacturing sites and external partners.
  • Oversee investigations of deviations, CAPAs, and change controls for compliance.
  • Provide technical oversight for process validation and lifecycle management.
  • Review and approve technical documents like tech transfer packages and regulatory support documents.
  • Input strategically into control strategies and continuous improvement initiatives.

Benefits

  • Comprehensive health benefits package including medical, dental, and vision coverage.
  • Life and disability benefits essential for employee security.
  • 401(k) plan with company contributions to support retirement savings.
  • Generous paid time off, including vacation, holidays, and sick leave.
  • Paid parental leave to support family needs.
Full Job Description
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
  • Respect one another and act as one
  • Learn, adapt, and win
  • Know someone's health is in our hands
  • Own the solution and make it happen

The pay range for this position is between $111,000 and $185,000 annually.

Actual base pay offered may vary depending on a number of factors such as job-related knowledge, skills and experience. Employees in this position are eligible for a discretionary performance-based cash incentive, and depending on the level of the role may be eligible for a discretionary annual equity award. Benefits for this position include a comprehensive health benefits package that includes medical, prescription drug, dental, and vision coverage. Other offerings include life and disability benefits, pre-tax accounts, a 401(k) with company contribution, and a variety of other benefits. In addition, employees are eligible for a generous time off package including paid vacation, holidays, sick days, and paid parental leave. Interested candidates can apply at Lantheus.com. Applications for this position will be accepted until 9/1/2026.

About Lantheus Holdings

Lantheus Holdings is a medical imaging company that develops, manufactures, and commercializes diagnostic imaging agents and products. The company's products are used in a variety of medical imaging procedures, including cardiovascular, oncological, and neurological imaging. Lantheus Holdings was founded in 1956 and is headquartered in North Billerica, Massachusetts. The company operates through two segments: Diagnostic Imaging and Therapeutic Imaging. The Diagnostic Imaging segment includes the production and sale of diagnostic imaging agents, while the Therapeutic Imaging segment includes the production and sale of therapeutic imaging agents. Lantheus Holdings is committed to developing innovative products that improve patient outcomes and has a strong track record of success in this area.
Learn more about Lantheus Holdings
Size
612 employees
Market Cap
$3.4 billion
Industry
Net Income
-$13.4 million
Founded
1956
5 Year Trend
+7.1%
Revenue
$339.4 million
NASDAQ

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