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Regulatory Affairs Senior Director – CMC Large Molecules

Company Name: Spectrum Pharmaceuticals Inc
Location: Irvine, CA
Job Type: Full-time Regular
Contact Name: Earl Falls
Phone: 702-835-6300
Fax:
Email: This email address is being protected from spambots. You need JavaScript enabled to view it.
Salary: Negotiable

Job Description:

This position will support global CMC regulatory activities related to investigational/commercial large molecule biologic products. This position will serve as a strategic business partner in providing regulatory CMC guidance to various development teams and for preparation of global CMC regulatory submissions to achieve timely approvals. This position will also be responsible for managing various Regulatory Affairs personnel at the Director and Manager levels who provide CMC support for the company’s biologic product portfolio.

RESPONSIBILITIES:

  • Accountable for strategy, planning, definition of content, and preparation of global regulatory eCTD CMC submissions and responses to Health Authority questions related to investigational and commercial biologics.
  • Identifies supporting documents required for global CMC submissions
  • Prepares CMC briefings for meetings with regulatory agencies
  • Directs CMC activities associated with global regulatory registration of biologic products
  • Provides CMC regulatory guidance and support to project core teams
  • Provides CMC strategic support for biologic products
  • Reviews CMC submission documents relative to regulatory guidance requirements
  • Monitors, assesses, and maintains current awareness of evolving CMC regulations and guidance documents; apprises management of the impact of these changes.
  • Manages direct reports, including recruitment, training, coaching, development, assignments, coordination of workload priorities, and performance
  • Other activities as assigned

 

Job Requirements:

SKILLS, EDUCATION AND EXPERIENCE:

  • S./B.A. required in Chemistry or Life Sciences; advanced degree preferred
  • Minimum of 10 years of related experience in biologics
  • Specific experience related to the preparation of global regulatory eCTD CMC submissions for investigational and commercial biologic products
  • Prior regulatory affairs managerial experience, with direct supervision of mid- to senior-level regulatory professionals, or equivalent managerial role required
  • Demonstration of positive interaction skills and work ethic
  • Proven communication skills (verbal and written)
  • Good organizational skills and attention to detail
  • Capable of working independently and in a team environment
  • Ability to manage multiple tasks simultaneously
  • Ability to successfully negotiate in a team environment
  • Good skills with MS Word, Excel, PowerPoint, and Document Management Systems

 

AVAILABILITY:

Must be available to work extra hours, as required, to complete projects

 

LOCATION:

  • Position is located in Irvine, CA or Cambridge, MA