Director of Supplier Quality Management & CDMO Oversight

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Bedford, MA, USA
In-Office
172K-287K Annually
Biotech • Pharmaceutical
The Role

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

The Director of Supplier Quality Management & CDMO Oversight is a senior quality leader responsible for establishing and executing the strategy that ensures all external partners—including Contract Development and Manufacturing Organizations (CDMOs), raw material suppliers, packaging vendors, and critical service providers—consistently deliver safe, compliant, and high‑quality pharmaceutical products. This role oversees the full lifecycle of external manufacturing quality, from supplier qualification and governance to ongoing performance monitoring, issue resolution, and continuous improvement.

The director serves as the primary quality interface with CDMOs and key suppliers, ensuring alignment with global cGMP requirements, regulatory expectations, and internal quality standards. This leader drives operational excellence, strengthens supply reliability, and supports successful regulatory submissions and inspections through robust oversight and proactive risk management.

This position is based in Bedford, Massachusetts and requires a presence on-site (two/three) days per week and is open to applicants authorized to work for any employer within the United States.

Key Responsibilities/Essential Functions

  • Lead the Supplier Quality Management function for Lantheus, setting a clear vision, strategy and process for the harmonized quality management of suppliers, contractors and consultants.
  • Develop and execute the global Supplier Quality and CDMO oversight strategy aligned with corporate quality objectives.
  • Establish and lead a comprehensive external quality governance model, including Quality Business Reviews, performance scorecards, and risk-based oversight plans.
  • Serve as the senior quality representative for external manufacturing within cross-functional leadership forums.
  • Oversee the qualification, approval, and periodic re-evaluation of CDMOs, raw material suppliers, and service providers.
  • Ensure quality agreements are established, maintained, and effectively implemented.
  • Provide quality oversight for all externally manufactured drug substances, drug products, intermediates, and clinical supplies.
  • Ensure robust management of deviations, investigations, CAPAs, change controls, and batch disposition activities.
  • Partner with CDMOs to ensure process robustness, data integrity, and adherence to cGMP and regulatory requirements.
  • Support technology transfers, scale-up activities, and process validation at external sites.
  • Lead quality risk assessments for external partners and implement mitigation strategies.
  • Drive continuous improvement initiatives across the external supply network to enhance quality performance and reliability.
  • Monitor and analyze supplier performance metrics, identifying trends and opportunities for improvement.
  • Ensure CDMOs and suppliers are inspection-ready and compliant with global regulatory expectations (FDA, EMA, MHRA, etc.).
  • Partner closely with Technical Operations, Supply Chain, Regulatory Affairs, Procurement, and Quality Assurance to ensure seamless external manufacturing operations.
  • Develop and maintain a strong partnership with key suppliers and act as the primary conduit for quality related issues from suppliers, contractors and consultants. Partner with Procurement and R&D, at an early stage, to identify development as well as commercial suppliers and contractors for new product introduction programs and redundancy in supply.
  • Act as the primary Quality representative for supplier management projects to support cost control programs, inventory management planning and compliance and business risk mitigation programs.
  • Oversee and ensure adherence to supplier quality management budget plan

Basic Qualifications

  • Requires a Bachelor’s degree in a scientific discipline and minimum of 8-10+ years proven experience managing CDMOs and global suppliers in a cGMP environment within the Pharmaceutical, Biotech and /or Medical Device industry. 
  • Minimum of 5 years people management experience preferred.
  • Incumbent must have excellent written, verbal and presentation skills. Must be able to interact effectively with all levels of management, both internal and external.
  • Must have a good understanding of cGMP requirements by FDA, EMA, ICH Q8, 9 and 10 etc.
  • Strong negotiating and collaboration skills are essential; incumbent must be able to influence and drive suppliers to high levels of performance.

Other Requirements

  • Strong analytical and problem solving skills with a risk-based mindset.
  • Experience with technology transfer, process validation, and commercial product lifecycle management
  • Exceptional communication, negotiation, and relationship building abilities.
  • Ability to influence at all levels and lead cross functional teams in a matrixed environment.
  • Strategic thinker with the ability to balance long term vision and operational execution.

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 $172,000-$287,000 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 May 8, 2026.

Lantheus is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression, sexual orientation, marital status, military service and veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any characteristic protected under applicable federal, state, or local laws and ordinances.

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 make a request to the Lantheus Talent Acquisition team at [email protected].

Lantheus is an E-Verify Employer.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Lantheus Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Lantheus and has not been reviewed or approved by Lantheus.

  • Healthcare Strength Benefits materials highlight comprehensive medical, dental, vision, mental‑health resources, wellness programs, and supporting tools. Employer‑verified listings also indicate coverage breadth across core health protections.
  • Retirement Support A 401(k) with company match is a core element and is described favorably within benefits details. Company disclosures indicate consistent access to welfare/benefit programs for eligible employees across levels.
  • Leave & Time Off Breadth The package features generous PTO, paid holidays, and paid parental leave, with flexible and hybrid work arrangements where roles allow. These offerings are presented as a comprehensive time‑off program.

Lantheus Insights

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The Company
HQ: Bedford, Massachusetts
1,252 Employees
Year Founded: 1956

What We Do

Lantheus is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes across oncology, neurology and cardiology. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and the United Kingdom, Lantheus has been providing radiopharmaceutical solutions for 70 years.

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