Quality Control Scientist

Integrated Resources Inc.; Sanford (NC); On-site; USD 70,000 - 100,000; Full time

Job summary

Integrated Resources Inc. is seeking a Quality Assurance Specialist for a vaccine manufacturing facility in North Carolina. The role involves overseeing GMP documentation, performing testing, analyzing results, and providing guidance to junior colleagues. Candidates should have a strong background in quality systems, complemented by a degree in a relevant scientific field.

Qualifications

• Minimum 5 - 8 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.
• BS/BA Degree in Science/related field required.
• Preferred University Degree in relevant fields.

Responsibilities

• Provides Quality Review/Oversight of site GMP documentation.
• Analyzes and interprets results for compliance.
• Plans and leads projects to ensure timely completion.

Skills

Quality Review

Documentation Oversight

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 Few Words About UsIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

• Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliance with global regulatory agencies and quality standards.

• Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples.

• Displays strong investigative or technological orientation with independence for design of projects/studies.

• Organizes and provides written and/or oral presentations of work with minimal input.

• Analyzes and interprets results, makes decisions regarding the accuracy, completeness and compliance.

• Responsible for final authorization/approval/release of documentation/equipment/processes.

• Assessing existing situations and suggesting improvements in the Quality systems to increase compliance throughout the facility

• Plans and leads projects to ensure their timely completion.

• Provide guidance/coaching to junior colleagues.

Qualifications

• Minimum 5 - 8 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.

• BS/BA Degree in Science/related field or other appropriate education/experience in biotech or pharmaceutical industry

• University Degree in the field of Engineering, Microbiology, Chemistry, Biotechnology, Biochemistry or Pharmacy or other appropriate education and experience in biotech or pharmaceutical industry is preferred.