QC Analyst III

Join a cutting-edge biotech leader in Portsmouth, NH, as a QC Analyst. This 8-month, 100% on-site contract role supports critical cGMP manufacturing by executing technical transfer activities, method/software validations, and data integrity initiatives in a fast-paced laboratory setting.

Responsibilities

• Lead method and software validations, including writing GMP procedures, executing test scripts, and authoring validation documents.
• Serve as a Subject Matter Expert (SME) for key laboratory software platforms.
• Execute root-cause analyses to troubleshoot complex technical software errors.
• Collaborate across cross-functional teams to translate operational needs into actionable priorities.
• Enforce rigorous Data Integrity principles across all laboratory workflows in strict compliance with GMP guidelines.

Requirements

• Bachelor's degree in a science-related discipline.
• Proven experience with specialized analytical software: SoftmaxPro, Empower, or SoloVPE.
• Direct GMP experience within the pharmaceutical or biotechnology industry.
• Proficiency with laboratory computer systems and data interpretation.

Qualifications

Preferred: Prior experience with GMP Quality Systems such as TrackWise or LIMS.

Skills

• Laboratory Information Management Systems (LIMS)
• Quality Control (QC)

Pay

$62.00 - $64.75 per hour

Schedule

9 AM to 5 PM, 100% on-site (8-month contract)

Benefits

• Medical, prescription, dental, and vision insurance
• AD&D and life insurance offerings
• Short-term disability
• 401K plan (all benefits based on eligibility)