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• Cambridge
• Negotiable
• Posted 8 days ago

Senior Compliance Auditor Role Description: Oversee and participate in audits, reporting on findings. Manage Quality Technical Agreements with critical suppliers. Conduct internal audits to meet GMPs, 820 standards, and company requirements. Lead and support supplier audits (onsite and remote) fo...

• Burlington
• Negotiable
• Posted 20 days ago

Overview: QA Leader to support the quality management systems and processes for a CRO based in Burlington. Working within pharma in both biologic development and cell and gene therapy and reporting directly to the Senior Director of Global Compliance. Role Responsibilities: Shape and expand our U...

• Cambridge
• Negotiable
• Posted about 1 month ago

Key Responsibilities: Documentation: Draft and revise procedures to meet regulations, cGMPs, and internal policies. Quality Standards: Apply and maintain quality standards and procedures for quality systems. cGMP Documentation: Review cGMP documents and lead or participate in their implementation...

• Cambridge
• Negotiable
• Posted about 2 months ago

Job Responsibilities: Lead and develop a team of Quality Assurance Specialists. Oversee final product release and adherence to cGMP regulations. Conduct inspections, review deviations, and manage corrective actions. Provide training and mentorship to team members. Collaborate effectively across d...

• Marlborough
• Negotiable
• Posted about 2 months ago

Regulatory Affairs Director Company Summary: My client, a reputable medical device company located in Marlborough, MA is seeking an experienced and driven Director of Regulatory Affairs. Their focus is on developing innovative laser devices and amplifiers. They are looking for this person to come...