Integrated Resources Inc.
QC Associate Scientist
Integrated Resources Inc., Sanford, North Carolina, United States, 27330
A Few Words About Us - Integrated 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.
This position is with my direct client
Job Description
RESPONSIBILITIES: • Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliance • Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples. • 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 projects and may initiate and develop plans to ensure their timely completion Qualifications
QUALIFICATIONS AND SKILLS NEEDED: • WORK EXPERIENCE/SKILLS: MINIMUM: 4 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry. • EDUCATIONAL BACKGROUND: MINIMUM: BS/BA Degree in Science/related field or other appropriate education/experience in biotech or pharmaceutical industry
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Job Description
RESPONSIBILITIES: • Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliance • Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples. • 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 projects and may initiate and develop plans to ensure their timely completion Qualifications
QUALIFICATIONS AND SKILLS NEEDED: • WORK EXPERIENCE/SKILLS: MINIMUM: 4 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry. • EDUCATIONAL BACKGROUND: MINIMUM: BS/BA Degree in Science/related field or other appropriate education/experience in biotech or pharmaceutical industry
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