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Job Details



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.




 

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