Director, Regulatory Affairs (FDA)

Director, Regulatory Affairs (FDA)

Location: Allendale, NJ - 07401 Duration: Full time Salary Range: $171,000 - $190,000 + 15% year-end bonus Client: Hitachi Chemicals Visa requirement: Only US citizens and Greencard holders Relocation assistance: No

Skills: FDA, GMP licensing, ICH Guidelines, Chemistry and Manufacturing Control (CMC) regulatory experience

Experience required: 10+ Years Essential Functions and Responsibilities

Coordinate projects and activities across regulatory support functions in Europe and Japan in order to formalize and harmonize regulatory processes, procedures, and infrastructure across the network.

Responsible to maintain up to date knowledge of regulatory requirements for cell therapy products in both clinical and commercial phases and communicate changes in requirements through the organization.

Plan, coordinate, author, and review any submissions to FDA to ensure company requirements and relevant FDA requirements are met.

Liaise with Project Managers and participate on global client project teams to properly plan for and support client submissions to regulatory agencies, including but not limited to strategies for technology transfer, process and method validation, and stability.

Participate in due diligence activities for potential licensing opportunities and acquisitions.

Manage GMP licensing for North America sites and supports global sites in obtaining appropriate licenses to market product in the US.

Critically review complex reports and change control documentation for regulatory and risk mitigation strategies.

Ensure compliance to Pharmacopeia through monitoring of changes and careful implementation at sites.

Develop relationships with Health Authorities through external engagement via professional organizations, conferences, and committees.

Coordinate across Global Quality and across Sites to support inspection coordination in order to obtain the appropriate GMP certifications for each site.

Work with the Global Head of Quality and Regulatory to plan for the long-term strategy and development of the Regulatory Affairs Department, including the development of client service offerings.

Provide regulatory training to site level associates as a Subject Matter Expert.

Partner with the Global Quality Systems organization in order to maintain the accuracy of the Global Quality Manual and Standards.

Provide review of Global Quality Manual and Standards, as well as global and regional SOPs as required in order to verify compliance to regulatory expectations and standards

Competencies

Excellent collaboration, agility, and adaptability

Strong leadership skills including influencing ability, driving results, commitment and execution, working in teams and a matrix environment

Demonstrated history of strong decision making

Well organized, adept at planning and working effectively within cross-disciplinary teams

Excellent oral, written, and verbal communication skills are required

Strong computer skills are required

Supervisory Responsibility

This is an individual contributor role in a heavily matrixed environment.

Qualifications:

BA/BS in the Life Sciences is required. MS or PhD in chemistry or biology and/or Regulatory Affairs is strongly preferred.

Minimum 7-10 years in Regulatory Affairs in an FDA Regulated Industry is required

Thorough knowledge of ICH Guidelines and FDA cGMPs and Guidelines is required. Knowledge of European and Japanese Health Authority requirements is strongly preferred

Chemistry and Manufacturing Control (CMC) Regulatory experience is a must.

Regulatory Affairs Certification preferred

Ability to work independently with minimal supervision is required

Proven interpersonal skills with face to face and remote teams

Minimum Required Training

The incumbent will be expected to complete all assigned GxP and Compliance related training in accordance with assigned due dates.