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Associate Director, Quality Compliance
Lantheus Billerica, MA
$190k-237k (estimate)
Full Time | Pharmaceutical 3 Weeks Ago
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Lantheus is Hiring an Associate Director, Quality Compliance Near Billerica, MA

Description

Lantheus is headquartered in Bedford, Massachusetts with offices in New Jersey, Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has helped physicians enhance patient care with its broad product portfolio.

Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostics, targeted therapeutics, and artificial intelligence (AI) solutions that empower clinicians to find, fight and follow disease. At Lantheus our purpose and values guide our behaviors in all interactions and play a vital role in creating a dynamic environment that contributes to our success. Every employee is crucial to our success; we respect one another and act as one knowing that someone's health is in our hands. We believe in helping people be their best and are seeking to bring together a diverse group of individuals with different viewpoints and skill sets to be a part of a productive and inclusive team.

Summary of Role

This role is responsible for providing leadership and compliance oversight for Lantheus' in-house and contract manufacturing activities and processes. The individual will manage and provide direction to one or more direct reports and interface with cross-functional teams, ensuring that processes and activities are performed in compliance with company policies, procedures, standards and applicable local, state, federal, and international regulations governing drug products and medical devices. This role will closely interact with cross-functional colleagues across multiple sites.

Key Responsibilities/Essential Functions

  • Manages the internal audit program, inspection readiness and external audits / inspections, Compliance Surveillance, Quality metrics, Quality Management Review (QMR), and other compliance activities as assigned.
  • Acts as Subject Matter Expert on applicable standards and regulations for the organization.
  • Manages inspection readiness and manages regulatory inspection processes relating to cGMP including, but not limited to, FDA, MHRA, EMA, Health Canada, and Notified Body, across multiple sites. Provides corporate training on inspection readiness, inspection process and best practices.
  • Develops and manages the internal auditing program to ensure a constant state of compliance. Plans and executes compliance audits of internal operations as they relate to GxPs to ensure compliance with policies, procedures, and regulatory requirements; drives timely completion of associated corrective actions. Track and trend multi-site compliance issues to assure alignment with corporate standards.
  • Manages the Compliance Surveillance program, tracking and trending new and changed regulations, agency guidance documents, industry standards, etc., identifying impact to Lantheus and driving resolution to close gaps.
  • Respond in a timely manner to compliance concerns and contribute to problem resolution.
  • Manages the creation and maintenance of compliance metrics, development of trend data of audit / inspection observations and communication of results expediently to applicable groups.
  • Identify areas of improvement and participates in process improvement initiatives. Implements quality and process improvements evaluating multiple perspectives. Creates new processes aimed at continual improvements, supporting a LEAN company culture. Manages multiple projects, realigning resources and priorities to meet challenging timeframes.
  • Manages the range of performance management processes for direct reports. Contributes to budgetary processes, including efficiency opportunities, in collaboration with leadership.
  • Other duties, projects and activities as assigned.

Basic Qualifications

  • Bachelor's degree in a related medical, science or business discipline and minimum 10 years' functional experience in Quality, Regulatory or comparable compliance discipline within the pharmaceutical, biopharmaceutical, medical device, or equivalent industries; or equivalent combination of education and experience.
  • Demonstrated proficiency and knowledge of cGMP, ICH, and other US and worldwide regulatory requirements.
  • Previous people management and/or team leadership experience 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
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

Job Summary

JOB TYPE

Full Time

INDUSTRY

Pharmaceutical

SALARY

$190k-237k (estimate)

POST DATE

06/08/2024

EXPIRATION DATE

08/07/2024

WEBSITE

lantheus.com

HEADQUARTERS

NORTH BILLERICA, MA

SIZE

200 - 500

FOUNDED

1956

TYPE

Public

CEO

MARY ANNE HEINO

REVENUE

$200M - $500M

INDUSTRY

Pharmaceutical

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About Lantheus

Lantheus engages in developing, manufacturing, selling and distributing diagnostic image agents and products.

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