QA Specialist – Quality Data Reviewer King of Prussia, PA Posted: 6/2/2026
Job Description
Job ID#:
8378
QA Specialist - Quality Data Reviewer
Location: Upper Merion (King of Prussia), PA Schedule: Fully Onsite | Monday-Friday | Day Shift (8-hour schedule) Pay Rate: $22.50 - $28.00 per hour
Alphanumeric is hiring a QA Specialist - Quality Data Reviewer to work onsite in Upper Merion (King of Prussia), PA with a global pharmaceutical organization dedicated to improving lives through innovative healthcare and medical advancements.
This role is ideal for a detail-oriented quality professional who thrives in a regulated laboratory environment and has a strong understanding of data integrity, cGxP requirements, and laboratory operations. The successful candidate will play a critical role in ensuring laboratory data is accurate, complete, compliant, and audit-ready while supporting product quality and batch release activities.
Responsibilities
Review laboratory data and documentation to ensure accuracy, completeness, and compliance with internal procedures and regulatory requirements.
Apply ALCOA+ data integrity principles during data review activities.
Support timely batch release by ensuring quality review activities meet established turnaround times.
Manage data lifecycle activities, including review, approval, reconciliation, and archiving of laboratory records.
Identify opportunities to improve the efficiency and effectiveness of data review processes.
Participate in internal audits, inspections, and compliance activities as required.
Maintain tracking systems and review metrics to provide visibility into progress, priorities, and outstanding items.
Collaborate with laboratory, quality, and cross-functional stakeholders to align on timelines and quality expectations.
Assist with training and mentoring team members on quality processes and data review requirements.
Participate in team meetings and provide updates, insights, and recommendations to support continuous improvement initiatives.
Ensure all reviewed documentation meets internal and external standards for accuracy, clarity, and completeness.
Job Requirements
Required Qualifications
Bachelor's degree in Biology, Biochemistry, Microbiology, or a related scientific discipline OR equivalent industry experience.
Minimum of 2 years of pharmaceutical, biotechnology, laboratory, or quality-related experience preferred.
Strong attention to detail and ability to manage high volumes of data review activities.
Understanding of cGxP regulations, data integrity requirements, and ALCOA principles.
Experience working within regulated laboratory environments.
Strong organizational, analytical, and problem-solving skills.
Excellent written and verbal communication skills.
Ability to work independently and effectively with minimal supervision.
Proficiency with Microsoft Excel, Word, and PowerPoint.
Preferred Qualifications
Experience with laboratory systems such as:
SAP / ERP
LES (Laboratory Execution Systems)
WebStatistica
Empower
Hamilton
Experience supporting analytical testing and laboratory operations, including:
Separations: HPLC, CGE, CE-SDS, cIEF
Immunoassays: ELISA, qPCR, SPR, Bioassays
Compendial Testing
Microbiology: Bioburden, Endotoxin
What We're Looking For
Exceptional attention to detail
Strong data review and data integrity mindset
Ability to prioritize multiple tasks and meet deadlines
Collaborative team player with leadership potential
Commitment to quality, compliance, and continuous improvement
If you're passionate about quality, data integrity, and supporting life-changing pharmaceutical products, we'd love to hear from you.