Director, Regulatory Affairs

Date: Nov 22, 2022

Location: US-NJ-Bridgewater, New Jersey, US

Company: Bausch & Lomb

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. 

 

Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries , extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. 

Position Summary:

The Regulatory Affairs – CMC Director independently manages all regulatory CMC aspects of Bausch + Lomb Company Pharmaceutical products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices.  The Director is responsible for the regulatory CMC strategy of submissions for all products under his/her responsibility as well as managing interactions with regulatory authorities on CMC issues.

 

Key Responsibilities:

 

  • Formulate, lead and drive CMC regulatory strategy for development projects or marketed products with a focus on creativity and innovation, maximizing the business benefit balanced with regulatory compliance.
  • Proactively communicate CMC regulatory strategy, key issues and any other critical topics throughout the life cycle  to interdisciplinary project teams and to appropriate management level in Regulatory Affairs, R&D, TechOps and Supply Chain as appropriate in an a timely manner.
  • Lead and drive all CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products. Make quality regulatory decisions, balancing risks and benefits.
  • Identify as early as possible, the required documentation and any content, quality and/or timeline issues. Negotiate the delivery of approved technical source documents in accordance with project timeline.
  • Coordinate with Regulatory Operations to ensure timely and accurate submissions to Regulatory Authorities.
  • Manage interactions with FDA on CMC issues.
  • Provide regulatory support to other company functions during Regulatory Authority inspections.
  • Serve as Regulatory Affairs representative on facility/site Local Change Management Boards.
  • Participate in assigned due diligent business activities.
  • Review and provide input on proposed health authority guidance documents on CMC issues.
  • Other job responsibilities as needed

 

 

Qualifications:

  • Knowledge of pharmaceutical industry regulatory affairs CMC discipline throughout the product lifecycle, with awareness of preclinical, clinical, commercialization, and operations.
  • Knowledge of current and emerging issues and trends of the pharmaceutical regulatory environment.
  • Capability to react quickly to changes in the regulatory environment and make strategic recommendations to minimize risk to the business.
  • Ability to influence external regulatory stakeholders and shape the external regulatory environment.
  • Ability to interpret Regulatory Authority policies and CMC guidance and correctly apply them as appropriate in product development and post-approval activities.
  • Ability to influence and partner with cross-functional teams.
  • Ability to take innovative ideas from proof of concept to promote a successful product regulatory CMC submission and increase probability of regulatory approval.
  • Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly and conclusions are adequately supported by data.
  • Ability to assess project risks, and where appropriate, recommend contingency plans and strategies to mitigate regulatory risks.
    Self-motivated, detail-oriented and capable of working independently.
  • Demonstrated ability in analytical reasoning and critical thinking skills.
  • Strong business acumen and ability to see the business drivers outside of Regulatory Affairs.
  • Excellent communication skills; both oral and written.
  • Strong interpersonal skills with the ability to influence others in a positive and effective manner.
  • Demonstrated ability to contribute to a continuous learning and process improvement environment.
  • Capacity to react quickly and decisively in unexpected situations.
  • 12+ years pharmaceutical industry and 10+ relevant regulatory CMC experience.
  • Bachelor’s degree in science, bio-chemical engineering, pharmacy or other health related field.
  • Advanced degree highly preferred ( MS, Pharm.D, Ph.D. or equivalent)

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

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