Supplier Quality Senior Specialist

Posted 5 Days Ago
Be an Early Applicant
Bedford, MA, USA
Hybrid
111K-185K Annually
Senior level
Biotech • Pharmaceutical
The Role
Manage supplier quality lifecycle for domestic and international suppliers (CMOs, APIs, raw materials, 3PLs). Serve as primary contact for 3PL/pharma partners, oversee supplier performance, lead supplier qualification/onboarding, handle deviations and CAPAs, support supplier change control, audits, and metrics reporting, and drive continuous improvement to maintain compliant vendor management and supply risk mitigation.
Summary Generated by Built In

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

The Supplier Quality Senior Specialist is responsible for maintaining Lantheus’s Supplier Quality Management (SQM) program, ensuring that systems, processes and procedures between Quality, Supply Chain, Technical Operations and R&D are compliant and aligned with business needs. This Senior Specialist is responsible for acting as the primary point of contact and relationship manager for Third Party Logistics (3PL) and Pharma Partners. They are also responsible for developing and managing an Approved Vendor List and ensuring procedures are in place for supplier lifecycle management, including initial assessment, qualification and onboarding, monitoring and offboarding, with continuous improvement initiatives. Domestic and international suppliers consist of Contract Manufacturing Organizations (CMO), drug substance precursors, active pharmaceutical ingredient (API) providers, raw material and component suppliers, contractors, 3PL and service providers.

The Supplier Quality Senior Specialist oversees supplier performance on an ongoing basis, implements a program of monitoring and continuous improvement and, if necessary, eliminate suppliers from the approved vendor list. This Senior Specialist executes all actions that contribute to the success of maintaining a compliant vendor management program.  They also maintain oversight and execution of all assigned Corrective and Preventative actions related to Supplier Quality management.

The position can be either remote or hybrid, with occasional onsite requirements at the department location in Bedford, Massachusetts.

Key Responsibilities/Essential Functions

  • Adhere to existing supplier lifecycle management program to ensure appropriate controls, processes and procedures are developed, implemented and maintained to ensure full compliance with regulatory requirements and alignment with industry best practices.
  • Serve as primary point of contact for 3PL and Pharma Partners.
  • Own and manage 3PL/Pharma Partner relationships; attend and/or own periodic touchpoints.
  • Support external audit planning, including risk-based execution and observation remediation.
  • Oversee supplier performance and quality data sources and metric reporting to identify quality issues and trends, as well as implement corrective actions and effectiveness criteria to hold suppliers accountable to promised performance improvement plans.
  • Own and resolve supplier-related deviations and CAPAs relating to non-conforming materials and services to identify true root causes and drive timely closure with suppliers.
  • Oversee supplier change management program, ensuring cross-functional participation and timely implementation to meet compliance standards and business needs.
  • Serve as Quality lead for new vendor triage process and provide Supplier Quality review of new material setup in GxP systems
  • Support disposition of discrepant, damaged, or expired supplier materials as
  • Assure planned changes to supplier management processes are fully approved and compliant with Lantheus procedures and regulatory guidelines.
  • 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.
  • Ensure adherence to supplier quality management budget plan
  • Function as an internal consultant and resource for site training/education coordination needs, including providing leadership and information to operations.
  • Serves as Subject Matter Expert for internal Committees and Boards as required in support of supplier management as determined by business need.

Basic Qualifications

  • Requires a BS degree in a scientific discipline and minimum of 7+ years’ experience in a GMP environment, preferably in a Quality- related discipline or Supplier Quality Management within the Pharmaceutical, Biotech and /or Medical Device industry, or equivalent combination of education and experience.
  • 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.
  • Must have demonstrated experience with Quality Management System databases.
  • Requires the ability to work independently to own projects and execute to 100% completion with minimal supervision.
  • Strong negotiating and collaboration skills are essential; incumbent must be able to influence and drive suppliers to high levels of performance.

Other Requirements 

  • Travel to suppliers (about 25%) will be required based on business needs.
  • Strong understanding of principles of Analytical/Chemistry required to support Supplier Analytical Testing and method development preferred but not required.

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 July 23, 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.

Skills Required

  • BS degree in a scientific discipline and minimum 7+ years' experience in a GMP environment in Quality or Supplier Quality Management within Pharmaceutical, Biotech or Medical Device industry (or equivalent)
  • Excellent written, verbal and presentation skills with ability to interact effectively with all levels of management
  • Good understanding of cGMP requirements by FDA, EMA, and ICH Q8, Q9 and Q10
  • Demonstrated experience with Quality Management System databases
  • Ability to work independently to own projects and execute to completion with minimal supervision
  • Strong negotiating and collaboration skills with ability to influence suppliers to meet performance expectations
  • Travel to suppliers (~25%) as required by business needs
  • Strong understanding of analytical/chemistry principles to support supplier analytical testing and method development

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.

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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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