Manager, Regulatory Affairs, Labeling - Hybrid

Lantheus
Bedford, MA, US
Full-time

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

Responsible for the development, maintenance and implementation of global product labeling components and applying knowledge of global regulations to ensure high quality and compliant labeling documents.

Key Responsibilities / Essential Functions

  • Provides leadership to the Regulatory labeling team in the creation and maintenance of global product labeling components.
  • Collaborates with other functional work teams , Supply Chain, Operations, Commercial and Clinical, providing regulatory guidance to aid in the preparation and submission of global product labeling materials.
  • Reviews labeling for compliance with applicable region’s labeling regulations and requirements. Make recommendations aimed at ensuring compliance.
  • Oversees activities within the labeling management system.
  • Serves as the key contact for global product labeling documentation materials and questions, ensuring they are completed in accordance with regulations.
  • Supports metrics to track the effectiveness of the labeling review process and provide recommendations as necessary for process improvements.
  • Employs a current understanding of our product offerings and the industry to impart beneficial, operational regulatory advice to a range of internal functional partners.
  • Maintains current knowledge of and ensure all work activities are conducted in compliance with the full range of related internal and external systems, technology, regulatory requirements and related policies and procedures.
  • Actively promotes safety rules and awareness. Always demonstrates good safety practices including appropriate use of protective equipment.

Reports and takes initiative to correct safety and environmental hazards.

  • Offer creative solutions and strategies, including risk mitigation strategies.
  • Evaluate regulatory risks and make recommendations relative to the labeling strategy.

Basic Qualifications

  • Bachelor’s degree with 4-6 years regulatory experience in a pharmaceutical environment.
  • Minimum 2 years’ experience in Regulatory Labeling
  • Knowledge of advertising, labeling, and promotion regulations and guidance for pharmaceuticals and devices.
  • Non-routine travel based on business need.

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

Lantheus is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law.

Lantheus is an E-Verify Employer in the United States. Lantheus will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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 .

LI-HYBRID

6 days ago
Related jobs
Promoted
The Mullings Group
Boston, Massachusetts
Remote

The new Global Regulatory Affairs Director is a critical hire to this organization leading PMA regulatory negotiations as the FDA point person as well as guiding clinical affairs, quality management, R&D, and all company team leaders toward successful pre-market approval. In collaboration with the V...

Promoted
Genabio Diagnostics
Bedford, Massachusetts

IVD or medical device FDA registration.International Device Licensing and Registrations.FDA and other inspection agencies as needed....

Lantheus
Bedford, Massachusetts

Provides leadership to the Regulatory labeling team in the creation and maintenance of global product labeling components. Responsible for the development, maintenance and implementation of global product labeling components and applying knowledge of global regulations to ensure high quality and com...

Promoted
Ladders
Somerville, Massachusetts

The Senior Regulatory Affairs Manager is a key member of the Legal, Regulatory Affairs & Compliance (LRAC) team. The Senior Regulatory Affairs Manager will also serve as the LRAC subject matter expert for all project implementation work associated with the assigned portfolio of regulations. The ...

MassGenics
Cambridge, Massachusetts

Regulatory Affairs Manager III. This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsibilities include preparation and compilation of submissi...

The Fountain Group
Cambridge, Massachusetts

The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Manager III for a prominent Pharmaceutical client of ours. This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations, and p...

Harvard University
Cambridge, Massachusetts

Supports the University’s regulatory and policy work at the state level and in Harvard’s host communities, including Cambridge and Boston. Establishes and maintains an internal network of colleagues across campus to analyze, interpret, and translate opportunities, risks, and questions associated wit...

Mass General Brigham
Somerville, Massachusetts

The Senior Regulatory Affairs Manager is a key member of the Legal, Regulatory Affairs & Compliance (LRAC) team. Regulatory Affairs Manager-(3291838). The Senior Regulatory Affairs Manager will also serve as the LRAC subject matter expert for all project implementation work associated with the assig...

jobbot
Boston, Massachusetts

Lead regulatory affairs activities, including the preparation of regulatory submissions and interactions with regulatory authorities. We are seeking Quality Assurance & Regulatory Affairs Manager to join our dynamic team. This is an exciting opportunity for a seasoned Quality Assurance & Regulatory ...

Alkermes
Waltham, Massachusetts

The Manager/Senior Manager of CMC Regulatory Affairs will be responsible for supporting commercial CMC and GMP activities for contracted manufactured products and Alkermes’ European office. The Manager/Senior Manager will also participate to formulate regulatory CMC strategies for product developmen...