Job Description

Review executed QC test records for molecular and cell-based assays. Ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.

Responsibilities:

• Review audit trails and reagent/equipment logbooks.
• Follow GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.
• Execute tasks precisely as defined in internal guiding documents, including SOPs and work instructions.

Requirements:

• Bachelor's degree in a relevant field.
• At least 5 years of experience in a cGMP laboratory setting, with hands-on experience in molecular biology and cell-based assays.

Preferred Qualifications:

• Excellent communication skills.
• Working knowledge of USP, ISO, FDA, and ICH guidelines.

About Us

We are a subsidiary of Chenega Corporation, providing Total Talent Solutions and Global staffing services. Our clients include Fortune 500 companies and prestigious educational institutions. We value diverse and inclusive workplaces.