Interim VP, Regulatory Affairs

Location: Hybrid schedule with onsite work in Berkeley Heights, New Jersey, United States; minimal travel.

Schedule: 20 hours per week for 4 months.

Company

hirify.global provides consulting solutions across the product lifecycle for biotech, medical device, and pharmaceutical organizations, covering regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology.

What you will do

• Provide senior strategic and hands-on regulatory affairs support on an interim basis.
• Set regulatory priorities across development programs.
• Lead preparation for FDA interactions and key regulatory submissions.
• Advise cross-functional teams on regulatory decisions.
• Provide oversight to keep regulatory work moving during a period of limited team capacity.

Requirements

• VP-level experience in regulatory affairs.
• Ability to provide strategic and hands-on support across development programs.
• Availability for 20 hours per week over a 4-month engagement.
• Ability to work onsite in Berkeley Heights, New Jersey, on a hybrid schedule.

Culture & Benefits

• Collaborative and entrepreneurial work environment.
• Commitment to diversity, equity, and inclusion.
• Support for remote working where appropriate, with hybrid collaboration encouraged for employees within a reasonable commute of an office.
• Minimal travel required.
• Applications are personally reviewed by the recruitment team without AI screening tools.