Join GrayMatter Partners, a fast-growing life sciences consulting company making an impact in biotech and pharma innovation. We partner with leading organizations to navigate regulatory requirements, ensure validated systems, and maintain the highest levels of quality throughout the product lifecycle. We're looking for passionate professionals to grow with us! We are seeking an experienced QA Reviewer to join our team. The ideal candidate will bring 5+ years of hands-on expertise in regulated life sciences environments.

Key Responsibilities:

• Provide Quality Assurance oversight and independent review of GxP activities within a life sciences environment.
• Review and approve quality documentation, including SOPs, batch records, deviations, CAPAs, change controls, and investigations.
• Assess documentation and processes for compliance with cGMP regulations, company procedures, and industry best practices.
• Identify potential quality risks, compliance gaps, and data integrity concerns and recommend appropriate actions. Qualifications
• Bachelor's degree in a scientific, engineering, or related discipline preferred.
• 5+ years of experience in Quality Assurance within the pharmaceutical, biotechnology, medical device, or other regulated life sciences industry.
• Strong working knowledge of cGMP regulations and GxP requirements.
• Experience reviewing and approving quality and manufacturing documentation.
• Experience with deviations, CAPAs, change controls, investigations, and/or audit activities. Perks and Benefits
• Medical, Dental, and Vision Insurance
• 401(k) Program
• PTO and Sick Time

Unique Culture and Values Pay:

$80,000.00 - $100,000.00 per year Application Question(s): Will you now or in the future require work visa sponsorship?

Work Location:

In person