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Biogen

Develops therapies for neurological disorders

Head of Global Product Quality - Biologics

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree and at least 12 years of experience in the pharmaceutical industry, including biological product development and/or production experience.
  • At least 7 years of experience in Quality associated with biopharmaceutical or pharmaceutical production.
  • At least 5 years of experience in people management and project management.
  • Extensive knowledge of good manufacturing practices (GMP), good clinical practice (GCP), good distribution practice (GDP), International Council for Harmonisation (ICH) guidelines, and international regulations.
  • Experience in an international matrix environment.
  • Technical expertise in manufacturing, testing, or technical development.
  • Strong written and verbal communication skills.
  • Ability to influence partners and stakeholders and negotiate effectively.

Responsibilities

  • Lead asset strategy and compliance best practices across products within a modality.
  • Review major regulatory submissions and help establish regulatory strategic plans.
  • Develop and cross-train staff to increase flexibility and support growth.
  • Execute specification strategy for regulatory submissions and address agency concerns.
  • Collaborate with cross-functional teams to support product specifications and shelf-life strategy.
  • Chair the Specification Review Board and ensure cross-functional vetting of specifications.
  • Represent Biogen at external forums to stay informed about emerging expectations and trends.
  • Ensure timely completion of Annual Product Reviews and Product Quality Reviews and conduct trend monitoring.
  • Support internal audits, certifications, and external audits of contract manufacturing organizations (CMOs).
  • Support combination product and device implementations in asset strategy.
  • Oversee product quality across Biogen’s biologics portfolio and ensure quality-related activities align with company policies and good manufacturing practice guidelines.
  • Facilitate execution of activities among business partners, the Chemistry, Manufacturing, and Controls (CMC) Asset Team, and the Quality organization.
  • Lead teams on existing and new products and technologies, aligning quality practices across the portfolio.

About the Company

Biogen

Develops therapies for neurological disorders

Biogen is a global biotechnology company focused on neuroscience. It discovers, develops, and delivers therapies for neurological disorders, such as multiple sclerosis and other neurodegenerative diseases. Its product process starts with research and development to identify potential drugs, followed by clinical testing and regulatory approval, ultimately leading to commercialization and patient treatment. Biogen differentiates itself through a long history (founded in 1978), a deep specialization in neuroscience, and an integrated pipeline that moves ideas from discovery to approved medicines, aiming to create value for shareholders while helping communities. The company’s goal is to advance therapies for neurological diseases to improve patients’ lives and generate sustainable value for stakeholders.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
1978

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