QA Compliance Specialist

This QA Compliance Specialist role is based in the Portsmouth, NH office. The candidate will support the Cell Therapy (CT) Quality Management System (QMS) and drive compliance, promote inspection readiness, and support key review boards.

Requirements

• Bachelor’s degree in Life Sciences, Chemistry, Biology, or a related field
• Working knowledge of GMP regulations and guidelines
• Strong written and verbal communication skills
• Experience with quality and enterprise systems such as DMS, TrackWise, SAP, Syncade, or similar platforms
• Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint)
• High attention to detail with strong organizational, analytical, and problem-solving skills
• Self-motivated and adaptable with ability to manage changing priorities and workload effectively
• Ability to work both independently and collaboratively within a team environment
• Sound judgment with ability to identify issues, present solutions clearly, and escalate when appropriate
• Experience in a regulated environment; cell therapy or biologics experience is a plus

Benefits

• Performance-related bonus
• Medical, dental and vision insurance
• 401(k) matching plan
• Life insurance, as well as short-term and long-term disability insurance
• Employee assistance programs
• Paid time off (PTO)