R&D Partners is seeking to hire a QC Analyst II, Micro in Philadelphia, PA. Your main responsibilities as a QC Analyst II, Micro: Perform daily GMP Quality Control laboratory testing activities at the i.

CTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform environmental monitoring of the cleanroom areas as scheduled.

Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Support technical problem-solving for issues pertaining to GMP Quality Control Support product stability programs, including execution of stability testing, stability data analysis and trending, and final reporting of stability data.

What we are looking for in a QC Analyst II, Micro: Bachelor s degree in a relevant discipline (biological sciences or equivalent) 3-8 years of experience in the pharmaceutical industry within a Quality Cont…Analyst, QC, Quality Control, Micro, Microbiology, Technology, Staffing

R&D Partners is seeking to hire a QC Analyst II, Micro in Philadelphia, PA. Your main responsibilities as a QC Analyst II, Micro: Perform daily GMP Quality Control laboratory testing activities at the i.

CTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform environmental monitoring of the cleanroom areas as scheduled.

Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Support technical problem-solving for issues pertaining to GMP Quality Control Support product stability programs, including execution of stability testing, stability data analysis and trending, and final reporting of stability data.

What we are looking for in a QC Analyst II, Micro: Bachelor s degree in a relevant discipline (biological sciences or equivalent) 3-8 years of experience in the pharmaceutical industry within a Quality Cont…Analyst, QC, Quality Control, Micro, Microbiology, Technology, Staffing

R&D Partners is seeking to hire a QC Analyst II, Micro in Philadelphia, PA. Your main responsibilities as a QC Analyst II, Micro: Perform daily GMP Quality Control laboratory testing activities at the i.

CTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform environmental monitoring of the cleanroom areas as scheduled.

Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Support technical problem-solving for issues pertaining to GMP Quality Control Support product stability programs, including execution of stability testing, stability data analysis and trending, and final reporting of stability data.

What we are looking for in a QC Analyst II, Micro: Bachelor s degree in a relevant discipline (biological sciences or equivalent) 3-8 years of experience in the pharmaceutical industry within a Quality Cont…Analyst, QC, Quality Control, Micro, Microbiology, Technology, Staffing

R&D Partners is seeking to hire a QC Analyst II, Micro in Philadelphia, PA. Your main responsibilities as a QC Analyst II, Micro: Perform daily GMP Quality Control laboratory testing activities at the i.

CTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform environmental monitoring of the cleanroom areas as scheduled.

Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Support technical problem-solving for issues pertaining to GMP Quality Control Support product stability programs, including execution of stability testing, stability data analysis and trending, and final reporting of stability data.

What we are looking for in a QC Analyst II, Micro: Bachelor s degree in a relevant discipline (biological sciences or equivalent) 3-8 years of experience in the pharmaceutical industry within a Quality Cont…Analyst, QC, Quality Control, Micro, Microbiology, Technology, Staffing