Quality Control Chemist / GMP QC Data Reviewer – Contract Role

Tap Growth ai; Norton (VA); On-site; USD 80,000 - 96,000; Full time

Job summary

A leading quality assurance firm in Virginia is seeking a Quality Control Analyst III Contractor to maintain high-quality standards through rigorous testing and analysis. Ideal candidates will have at least 4 years of experience in GMP Quality Control, a B.S. in a scientific field, and expertise in quality assurance methodologies. This position requires strong analytical skills and attention to detail. Apply now to contribute to our commitment to excellence.

Qualifications

• 4+ years in a GMP Quality Control function or equivalent experience.
• Experience in method transfer and/or analytical method implementation.
• Attention to detail to inform decision-making.

Responsibilities

• Perform routine and non-routine analytical assays.
• Support weekend laboratory operations.
• Maintain laboratory equipment and inventory.
• Review data timely and qualify as a data reviewer.
• Ensure smooth laboratory operations and support quality metrics.

Skills

Analytical testing

Quality assurance methodologies

Regulatory standards

Technical writing skills

Data analysis and interpretation

Education

B.S. in chemistry, biology, or biochemistry

Job description

We're Hiring: Quality Control (QCO) Analyst III Contractor!

We are seeking an experienced Quality Control Analyst III to ensure product quality and compliance through rigorous testing and analysis. The ideal candidate will have expertise in quality assurance methodologies, analytical testing, and regulatory standards to maintain our high-quality standards.

Location: Norton, MA
Work Mode: Work From Office
Role: Quality Control (QCO) Analyst III Contractor
Pay Scale: Up to $95,056 (Dependent on Experience)

What You'll Do:

• Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs
• Support a continuous operational schedule by supporting weekend laboratory operations (Analytical, Microbiology, Raw Materials).
• Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics
• Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations
• Ensure data are reviewed timely; qualify as a data reviewer to ensure timely and efficient data availability.

What We're Looking For:

• B.S. in chemistry, biology, or biochemistry, or related scientific field;
• Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent, relevant industry experience
• Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirable
• Demonstrated technical writing skills, with preference for technical writing of investigations
• Proficient in data analysis and interpretation, with excellent attention to detail to inform decision-making

Ready to make an impact? Apply now and let's grow together!