Quality Control Biochemistry Associate II

QC Associate II

Location: 5000 Davis Drive, Research Triangle Park, NC 27709

Schedule: Monday–Friday, 9:00 AM–5:00 PM

Pay Rate: $30–$38/hour, depending on experience

Contract Length: 6-month contract with potential for extension

Benefits: Weekly pay and healthcare benefits available

The QC Associate II will support Biochemistry Quality Control activities for large molecule products, contributing to testing, method transfer, validation, and laboratory operations within a GMP-regulated environment. This role is responsible for performing in-process and release testing, supporting investigations, and ensuring the integrity and accuracy of laboratory results.

The ideal candidate will have hands‑on laboratory experience, a strong understanding of quality systems and compliance requirements, and the ability to collaborate effectively with Quality, Manufacturing, and cross‑functional teams.

• Perform in-process and release testing of large molecule products.
• Execute method transfer and validation testing activities.
• Conduct analytical testing including:
  • pH
  • Appearance
  • Osmolality
  • Protein Concentration (UV, RI, and SoloVPE)
• Support laboratory investigations and perform testing related to investigational activities.
• Ensure accurate and timely documentation of testing activities and results.

• Support QC Biochemistry operations in alignment with business and manufacturing schedules.
• Assist with process validation initiatives and related testing activities.
• Collaborate with Quality and Manufacturing teams to support production timelines and quality objectives.

• Maintain effective laboratory systems to ensure data integrity and reliable test results.
• Adhere to all GLP and GMP requirements, company procedures, and quality standards.
• Contribute to continuous improvement initiatives and support audit readiness activities.

• Bachelor's degree in a scientific discipline preferred (Biology, Biochemistry, Chemistry, Microbiology, or related field).
  REQUIRED

• Master's degree with 2+ years of relevant laboratory or quality control experience, OR
• Bachelor's degree with 3+ years of relevant laboratory or quality control experience.

• Experience working in a GMP-regulated pharmaceutical, biotechnology, or life sciences environment.
• Knowledge of biochemistry testing methods and laboratory instrumentation.
• Experience supporting method validation, method transfer, and quality investigations.
• Strong attention to detail and documentation skills.
• Excellent verbal and written communication skills.
• Ability to work independently while collaborating effectively across departments.