Associate Director, Global Regulatory Affairs Cmc

vor 1 Woche

Zürich, Zürich, Schweiz ARIAD Vollzeit

Job Type:

Full Time
Job Level:

Senior
Travel:
Minimal (if any)

Global Regulatory Affairs (GRA) develops and executes innovative regulatory strategies to provide life-changing therapies to patients. GRA has a strategic role in all stages of global product development and across the Takeda Enterprise.


At Takeda, we strive to provide transformational opportunities for every member of our team, and we empower our people to take charge of their futures.

In an environment that fosters lifelong learning and a growth mindset, you'll have the support you need to thrive — at work and beyond.


Job ID R0117126
Date posted 03/26/2024
Location Zurich, Canton of ZurichAre you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an Associate Director, Global Regulatory Affairs CMC - Marketed Products in our Zurich office.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission.

As an Associate Director working on the Global Regulatory Affairs CMC team, you will be responsible and accountable for regulatory CMC development, registration and post-approval strategies, and a typical day will include:

OBJECTIVE:

  • GRA CMC member on Regulatory, Pharmaceutical Development, and Commercial project teams throughout commercial lifecycle. Ensures global strategies are successfully executed across both new product development and existing portfolio life cycle management.
  • Successfully communicates and negotiates with international Health Authorities as necessary, directly and indirectly.
  • Develops constructive relationships with and proactively communicates issues to key internal and external colleagues, including Alliance Partners.
  • Provides regulatory CMC expertise for new business development/due diligence activities.

ACCOUNTABILITIES:

  • Member of global crossfunctional teams which require experienced interpretation of applicable EMA/FDA/ICH/WHO/Global regulations to ensure CMC compliance within the organization.
  • Recommends direction for key operations and new initiatives in collaboration with local and global stakeholders.
  • Lead team members that define CMC content (data and documentation) requirements for regulatory submissions and reviews this content for conformance with established requirement.
  • Manages and develops staff, if required, including staff professional development and project oversight accountability.
  • Represents Takeda RA CMC in Health Authority meetings and leads preparation activities for meetings with Health Authorities on CMC related matters
  • Interacts directly with international Health Authorities, as required. Participates in and/or facilitates agency meetings.
  • Ensures project team colleagues, line management, and key stakeholders are apprised of developments that may impact regulatory success, exercising sound judgement and communicating in a professional and timely manner. Provides solutions to prevent recurrence of issues.
  • Stays abreast of current and evolving regulatory CMC requirements, applies this knowledge to assigned projects, and shares knowledge and experience with others to support their development.
  • Develops and maintains constructive relations with key internal and external colleagues, e.g. cross functional colleagues within Takeda, Alliance Partners, and Health Authority representatives.
  • Evaluate new business development opportunities or participate on due diligence teams
  • Proven ability to liaise with Regulatory Agencies, having served as lead in successful Agency Interactions related to CMC submissions and product development meetings; international experience preferred.
  • Evaluates change proposals for global regulatory impact and plans global variations and amendments.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

  • BS/BA Degree in a Scientific Discipline, Advanced Degree preferred.
  • 8+ years pharmaceutical Regulatory CMC experience including experience as an RA CMC product lead, or equivalent industry experience (e.g., Pharmaceutical Development, Analytical Development, Production, Quality Assurance).
  • Experience with pharmaceutical development of active pharmaceutical ingredient/drug substances or drug products, analytical characterization, process scaleup and/or regulatory registration of products is required.
  • Experience with global regulatory aspects of CMC involving undefined frameworks with medium technical complexity and defined scope. Proven ability to liaise with Regulatory Agencies having served as lead in successful Agency Interactions related to CMC submissions and product development meetings, international experience preferred.
  • Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and postmarket support.
  • Proven ability to provide strategic regulatory guidance to drug development, registration, and postmarket suppor

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