Overview
Quality Control Analyst Jobs in New Hampshire, United States at SoTalent
Title: Quality Control Analyst
Company: SoTalent
Location: New Hampshire, United States
Job Title: Quality Control Analyst
Location: New Castle, New Hampshire
Employment Type: Full-Time
Role Overview:
We are seeking a detail-oriented and experienced Quality Control Analyst to join our Quality Assurance team. This role plays a vital part in ensuring laboratory practices and documentation meet rigorous industry standards and regulatory requirements. The ideal candidate will bring a strong background in QA oversight, documentation review, and compliance within a Good Manufacturing Practice (GMP) environment.
Key Responsibilities:
Conduct on-the-floor QA reviews for Quality Control (QC) laboratory operations
Review and approve QC documentation, including test records, lab investigations, system suitability checks, stability reports, assay qualification protocols, and environmental monitoring data
Provide QA oversight for deviation investigations, discrepancy reporting, and corrective and preventive action (CAPA) implementation
Apply knowledge of GMP to evaluate and ensure alignment of QC processes with procedures and regulatory expectations
Maintain compliance with mandatory training and support training of team members
Manage or approve investigations and change controls related to QC activities
Review and approve master documents related to QC, including SOPs, forms, and specifications
Participate in Root Cause Analysis (RCA) processes to support effective and timely resolution of quality issues
Oversee quality change requests involving laboratory services
Collaborate with cross-functional teams to obtain documentation, provide updates, and ensure alignment with project timelines
Build and maintain strong working relationships with internal departments and external stakeholders
Support and execute project-based tasks as assigned
Perform additional duties as needed
Qualifications & Experience:
Bachelor’s degree in Life Sciences or a related field
5–10 years of experience in Quality Assurance or a similar role within a regulated environment
Demonstrated ability to review and approve QC documentation
In-depth understanding of GMP standards and regulatory requirements
Strong communication, interpersonal, and organizational skills
Ability to manage multiple tasks and projects effectively with minimal supervision
Experience with CAPA systems and Root Cause Analysis methodologies preferred
Proficiency in managing documentation, SOPs, and quality systems
This is an exciting opportunity to contribute to a dynamic and collaborative team that plays a critical role in maintaining product quality and regulatory compliance. If you are passionate about continuous improvement and quality excellence, we encourage you to apply.
