Senior GMP QA Scientist — Vaccine Manufacturing

Artech Information System LLC; Sanford (NC); On-site; USD 85,000 - 115,000; Full time

Job summary

A leading IT staffing company is looking for a Quality Sr. Scientist specializing in quality assurance. The role focuses on laboratory testing within a GMP environment to ensure compliance with regulatory standards. Ideal candidates should have 5-8 years of experience in the biotech or pharmaceutical industry and a relevant degree. Responsibilities include overseeing GMP documentation, performing various tests, and leading quality improvement projects. This position offers an opportunity to contribute to the development of high-quality pharmaceutical products.

Qualifications

• 5 - 8 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.
• Strong investigative or technological orientation.
• Experience with GMP documentation.

Responsibilities

• Providing Quality Review/Oversight of site GMP documentation.
• Perform testing including clinical and commercial products.
• Analyze and interpret results, making decisions regarding compliance.
• Plan and lead projects to ensure timely completion.

Skills

Quality Review/Oversight

Laboratory Testing

Analytical Skills

Project Management

Coaching

Education

BS/BA Degree in Science or related field

University Degree in Engineering, Microbiology, Chemistry, Biotechnology, Biochemistry, or Pharmacy

Job description

A leading IT staffing company is looking for a Quality Sr. Scientist specializing in quality assurance. The role focuses on laboratory testing within a GMP environment to ensure compliance with regulatory standards. Ideal candidates should have 5-8 years of experience in the biotech or pharmaceutical industry and a relevant degree. Responsibilities include overseeing GMP documentation, performing various tests, and leading quality improvement projects. This position offers an opportunity to contribute to the development of high-quality pharmaceutical products.