×
Register Here to Apply for Jobs or Post Jobs. X

Regulatory Compliance, Senior Manager

Job in Boston, Suffolk County, Massachusetts, 02101, USA
Listing for: Takeda Pharmaceutical
Full Time position
Listed on 2026-02-15
Job specializations:
  • Management
    Regulatory Compliance Specialist, Risk Manager/Analyst
Job Description & How to Apply Below

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description
About the role:

The Plasma-Derived Therapies (PDT) R&D Organization is dedicated to bringing forward new plasma-derived therapies for patients with immunologic, hematologic, and other complex diseases.

The Regulatory Compliance, Senior Manager ensures that the organization gains regulatory approval for new products and product amendments, and maintains the currency of product licenses and permits. This role involves monitoring regulatory developments, ensuring compliance, and preparing necessary documentation to support Takeda's mission.

How you will contribute:
  • As a Regulatory Compliance, Senior Manager in our PDT organization, you will ensure the organization is aware of and compliant with legislation and regulations pertaining to the business

  • Monitor and interpret regulatory developments, determining the impact on business operations and compliance programs

  • Implement compliance measures and ensure adherence to regulatory standards

  • Prepare, review, and approve regulatory compliance documents for internal and external audiences

  • Manage large projects or processes with limited oversight from the manager

  • Coach, review, and delegate work to lower-level professionals

  • Serve as a consultant to management and an external spokesperson on major matters

Minimum Requirements /

Qualifications:
  • BSc degree, preferred; BA accepted.

  • Advanced scientific degree (MSc, PhD, or Pharm

    D) preferred.

  • 6+ years of pharmaceutical industry experience. This is inclusive of 4 years of regulatory compliance or combination of 4+ years regulatory and/or related experience.

  • Proficient in regulatory compliance, capable of advising others and handling highly complex compliance issues independently.

  • Performs advanced Environment Health and Safety tasks independently, capable of coaching others and making improvement recommendations.

  • Leads new product development projects, advising on market analysis and customer needs, capable of managing complex situations and guiding others.

  • Capable of independently managing and improving organizational structures and processes, can coach others in effective organization.

  • Leads project management efforts in complex situations, advising and coaching others, and contributing to process improvements.

  • Advanced writing ability, capable of crafting well-structured content for a variety of complex scenarios and can mentor others in improving their writing skills.

  • Fully capable of executing complex risk analysis independently, advising on mitigation strategies, and coaching others in risk analysis methods and principles.

  • Fully capable of managing time in highly complex situations and can coach others on time management techniques and improvements.

  • Excellently manages tasks requiring high attention to detail, independently addresses complex scenarios, and advises others on maintaining precision.

  • Skilled in creating and delivering persuasive and impactful presentations in a variety of complex situations, able to mentor others in developing their presentation skills.

  • Advanced in auditing, capable of handling highly complex situations, making improvement recommendations, and coaching others.

  • As an expert professional within the organization, you develop innovative solutions to complex problems aligned with organizational objectives. Your work involves addressing intricate issues, requiring in-depth analysis and judgment. You also engage with key contacts outside your expertise area and contribute to the development of new concepts and standards. Operating with considerable autonomy, you serve as a consultant to management and an external spokesperson on major matters, often working independently and leading function teams or projects.

    Additionally, you play a role in training and mentoring junior staff.

More about us:

At Takeda, we are transforming patient care through the…

Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary