Senior Regulatory Affairs Specialist - SaMD & Software

Skills Alliance; New Jersey; Hybrid; USD 120,000 - 170,000; Full time

Job summary

Skills Alliance, a commercial stage organ technology company in New Jersey, seeks a Senior Regulatory Affairs Specialist (Software) to lead regulatory efforts for Digital Health, Software, Cybersecurity, and Electromechanical projects.

You will prepare submissions for FDA and Health Canada, interact with regulators, and track regulatory changes while coordinating with Manufacturing, Quality, R&D, Clinical, and Marketing teams.

Qualifications

• Bachelor’s degree or higher in Engineering, Life Sciences, or related field.
• 3–8 years of regulatory experience with Class II/III devices and software.
• Working knowledge of FDA processes for medical device compliance.
• Experience with SaMD, SiMD, cybersecurity, or electromechanical products.
• Strong regulatory strategy and submission writing skills.
• Understanding of GMP compliance.
• Experience working cross-functionally with Manufacturing, Quality, R&D, Clinical, and Marketing.

Responsibilities

• Providing regulatory support for Digital Health, Software, Cybersecurity, and Electromechanical projects.
• Supporting pre-market and post-market regulatory activities.
• Preparing submissions (IDE, IDE Supplements, PMA, PMA Supplements) for FDA and Health Canada.
• Interfacing directly with FDA and Health Canada on assigned projects.
• Tracking regulatory changes in the US and Canada.
• Communicating regulatory updates to internal and external stakeholders.
• Preparing summaries and visualizations for senior management.

Skills

Regulatory strategy

Submission writing

Cross-functional collaboration

GMP knowledge

SaMD/SiMD experience

Education

Bachelor’s degree or higher in Engineering/Life Sciences

Job description

Skills Alliance, a commercial stage organ technology company in New Jersey, seeks a Senior Regulatory Affairs Specialist (Software) to lead regulatory efforts for Digital Health, Software, Cybersecurity, and Electromechanical projects.

You will prepare submissions for FDA and Health Canada, interact with regulators, and track regulatory changes while coordinating with Manufacturing, Quality, R&D, Clinical, and Marketing teams.