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Senior Manager Global Regulatory Affairs CMC

CSL

Bern, Bern, Switzerland; King of Prussia, PA; Waltham, MAOnsitePosted 20 days ago
Full TimeSenior LevelRegulatory AffairsBiotechnology
Original posting ↗

Summary

The Senior Manager Global Regulatory Affairs CMC - Biological & Non-Biol. Products partners closely with CSL's R&D, Manufacturing, Quality, and Regulatory Affairs stakeholders to address regulatory strategy challenges and deliver innovative, timely regulatory solutions that meet evolving CMC regulatory and compliance requirements for the assigned product portfolio.

Job description

Main Responsibilities and Accountabilities

  • Lead the global regulatory CMC strategy across the assigned development and commercial biological & non-biol. product portfolio, collaborating closely with cross-functional leaders in Global Regulatory Affairs CMC, Global Regulatory Affairs, R&D, Quality, Global Operations, and other business functions.
  • Manage the development and submission of high-quality, compliant CMC regulatory submissions and submission components, including new marketing applications, clinical trial applications, variations/supplements, periodic compliance reports and renewals.
  • Ensure accurate and timely change control assessments of change control notifications in CSL's quality management system for biological & non-biol. product-related change controls.
  • Leverage external insights to refine strategies and implement innovative regulatory approaches that enhance CSL's competitive positioning.
  • Represent CSL in official regulatory CMC capacities, acting as an authorized official or responsible person in interactions with regulatory agencies.
  • Maintain strong, positive relationships with regulators and ensure timely responses to inquiries and requests.
  • Develop strategic and tactical plans for Global Regulatory Affairs CMC, advising leadership and CSL stakeholders on regulatory requirements and their implications for project timelines, compliance, and business strategy.
  • Contribute to the evaluation of new business opportunities in collaboration with development teams.
  • Provide regulatory consultation to internal CSL functions, including Global Operations, R&D, and IT, to support the design and implementation of business processes that ensure regulatory compliance and operational excellence.
  • Provides tactical and strategic regulatory input and guidance, including active participation in problem solving analysis by assessing and proposing alternative solutions to issues and prepare contingency plans while still meeting regulations.
  • Maintains an ongoing and interactive relationship with regional and local regulatory teams to assure that all aspects of the company's regulatory activities are conducted in full compliance with applicable regulations and at the highest level of ethical standards.
  • Ensure regulatory policies and procedures are developed and implemented in accordance with applicable international standards and requirements.
  • Support the creation and execution of regulatory policies, processes, and SOPs that meet global regulatory requirements while driving operational efficiency and effectiveness.
  • Support the outsourcing of regulatory activities, including submission quality assurance, to ensure timely and compliant delivery of services aligned with business and regulatory requirements.

Position Qualifications and Experience Requirements

  • A bachelor's degree in biological or chemical sciences, or a related field is required; an advanced degree (e.g., MS, PhD) is strongly preferred.
  • Over 5 years of progressive experience in regulatory roles within the biologics or plasma industry, demonstrating increasing levels of responsibility.
  • Strong technical foundation with in-depth knowledge of global regulations and international standards governing drug product development, manufacture, registrations, and life-cycle management.
  • Proven expertise in authoring, reviewing, and managing regulatory submissions ensuring accuracy, compliance, and timely delivery.
  • Demonstrated ability to lead cross-functional teams and collaborate effectively with key stakeholders.
  • Skilled in motivating, mentoring, and guiding diverse teams within a matrixed organizational structure, fostering a culture of accountability and excellence.
  • Exceptional oral and written communication skills, with a strong ability to negotiate, influence, and represent regulatory positions effectively.
  • Committed to the highest standards of compliance, integrity, and adaptability, with a strong focus on aligning regulatory strategy with evolving business needs.
  • Ability to use precedent and previous experience to develop innovative and flexible approaches to achieve goals.

Requirements

  • Bachelor's degree in biological or chemical sciences or related field
  • Advanced degree (MS, PhD) strongly preferred
  • Over 5 years of progressive experience in regulatory roles within biologics or plasma industry
  • In-depth knowledge of global regulations and international standards governing drug product development, manufacture, registrations, and life-cycle management
  • Proven expertise in authoring, reviewing, and managing regulatory submissions
  • Demonstrated ability to lead cross-functional teams and collaborate with key stakeholders
  • Skilled in motivating, mentoring, and guiding diverse teams within a matrixed organizational structure
  • Exceptional oral and written communication skills with ability to negotiate and influence
  • Commitment to high standards of compliance, integrity, and adaptability

Company overview

CSL Limited is an Australian multinational specialty biotechnology company that researches, develops, manufactures, and markets products to treat and prevent serious human medical conditions. Founded in 1916 as Commonwealth Serum Laboratories, CSL has grown to become the world's fifth largest biotechnology company with operations in over 35 countries. The company specializes in blood plasma derivatives, vaccines, antivenoms, and cell culture reagents used in medical and genetic research applications. CSL operates through several key divisions including CSL Behring (focusing on rare and serious diseases), CSL Seqirus (one of the world's largest influenza vaccine providers), CSL Plasma, and CSL Vifor. With over 32,000 employees globally, CSL maintains a strong R&D pipeline and has invested over US$3.3 billion in research and development over the past five years. The company is publicly traded on the Australian Securities Exchange and has its global headquarters in Parkville, Melbourne, Australia.

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