Lantheus Holdings

Quality Compliance Sr Specialist

Lantheus Holdings$111K — $185K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor of Science in a technical discipline or equivalent experience.
  • 7+ years in quality systems or assurance in pharmaceutical or medical device industries.
  • Proven experience with Annual Product Quality Reports and medical device post-market surveillance programs.
  • Strong knowledge of regulatory requirements like cGMP, ICH, ISO 13485, and ISO 14971.
  • Experienced in document control within an electronic quality management system.
  • Prior experience conducting quality system audits and complaint investigations.
  • Detail-oriented, organized, and self-motivated individual.

Responsibilities

  • Draft and submit APQR and PMSR reports for management approval.
  • Conduct internal and external quality audits.
  • Enhance Inspection Readiness program through training and walkthroughs.
  • Review documents for regulatory compliance and author revisions.
  • Lead the Compliance Surveillance Review program.
  • Analyze and trend Quality System KPIs for reporting.
  • Manage the lifecycle of corporate GxP documents, including creation and revision.
  • Facilitate corporate document requests across departments.
  • Initiate and track product quality complaints in the QMS.
  • Collaborate with various departments for timely complaint resolution.
  • Champion continuous improvement initiatives within the Quality Management System.
  • Promote safety practices and correct hazards.

Benefits

  • Comprehensive health benefits including medical, dental, and vision coverage.
  • Life and disability benefits.
  • 401(k) plan with company contributions.
  • Generous paid time off including vacation, holidays, and parental leave.
  • Additional pre-tax accounts and incentives.
Full Job Description
Summary of role
We are seeking a Quality Compliance Senior Specialist who will be responsible for overseeing and authoring Annual Product Quality Reports (APQR) for Lantheus commercial products, performing internal Quality System audits, leading the Compliance Surveillance Review Board, authoring and revising Quality System Documentation, as well as supporting document control activities including overseeing the document life cycle management of corporate policies and procedures within the Lantheus electronic quality management system.

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

Responsibilities
  • Supports writing and submitting Annual Product Quality Reports (APQR) and Post Market Surveillance Reports (PMSR) to senior management for approval.
  • Support internal audits and external audits.
  • Support the Inspection Readiness program including the training of personnel, and conducting walkthroughs to ensure facilities are inspection ready.
  • Review documents for compliance with regulatory guidelines and applicable standard operating procedures, authoring document changes as needed.
  • Lead Lantheus' Compliance Surveillance Review program
  • Perform trending of Quality Systems and Compliance KPIs for reporting into monthly and quarterly management reviews.
  • Maintain control of corporate level GxP documents throughout their lifecycle including creation, review, approval, issuance, revision, archival, and obsolescence.
  • Triage and route corporate level document requests across departments.
  • Initiates product quality complaints in the Lantheus Quality Management System (QMS)
  • Collaborate with Technical Support, Engineering, Analytical Laboratories, Manufacturing, Validation, Customer Service and Regulatory Affairs groups to ensure timely complaint investigations and closure.
  • Champion quality initiatives to continually support and improve the Quality Management System.
  • Actively promotes safety and awareness. Always demonstrates good safety practices including the appropriate use of protective equipment. Reports and takes initiative to correct safety and environmental hazards.
  • Actively demonstrates Lantheus values.
  • Other duties as assigned.

Basic Qualifications
  • Bachelor of Science in a technical discipline or equivalent combination of education and experience.
  • Minimum of 7 years of experience in quality systems, quality assurance or other quality discipline in the pharmaceutical, medical device, or biological industries.
  • Experienced in generating Annual Product Quality Reviews for commercial pharma products and/or experience with medical device post market surveillance programs.
  • Demonstrated proficiency and knowledge of cGMP, ICH, ISO 13485, ISO 14971, and other US and worldwide regulatory requirements.
  • Experienced in performing document control activities within an electronic quality management system.
  • Previous experience performing quality system audits.
  • Experienced in investigating Customer Product Quality Complaints, effectively communicating in written form, and collaborating with various internal and external business partners in problem resolution.
  • Organized, detail oriented and self-motivated.
  • Experienced with supporting pharmaceutical and/or medical device GMP compliance regulatory inspections.

Preferred Qualifications
  • Good planning and project management skills.
  • Good verbal, written and presentation skills at all levels both internally and externally.
  • Ability to communicate effectively at a variety of levels of the organization, as well as coach and mentor members of GxP functions on compliance requirements and topics.
  • Must be detail oriented with the ability to multitask and respond to ever changing priorities.
  • Ability to work independently and drive on time completion of responsibilities and assigned tasks.

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 - $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 30, 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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