Quality Control Analyst
Infotree Global Solutions · Frederick, Maryland, United States
FULL TIMEpermanent
Job Description
We are seeking a QC Analyst to support laboratory testing and quality control activities in a biotechnology or pharmaceutical environment. The ideal candidate will have experience with analytical testing, GMP compliance, laboratory documentation, and quality systems.
Apply (by clicking the relevant button) after checking through all the related job information below.
Key ResponsibilitiesPerform analytical testing of raw materials, intermediates, and final products using techniques such as Flow Cytometry, ELISA, qPCR, and cell-based bioassays.Review laboratory data, test records, and documentation to support in-process testing and drug substance and drug product release.Assist with laboratory instrument calibration, routine maintenance, and laboratory readiness.Prepare and revise Standard Operating Procedures (SOPs), qualification and validation protocols, and reports.Support out-of-specification (OOS) investigations, deviations, and root cause analysis.Monitor compliance with GMP requirements, established procedures, and applicable quality systems.Review proposed changes to laboratory procedures, methods, and systems.Track laboratory metrics and support continuous improvement initiatives.Communicate testing updates and collaborate with scientific and technical teams.QualificationsBachelor’s degree; OR an associate degree with at least 2 years of relevant biotechnology or related industry experience, including Quality Control experience; OR a high school diploma with at least 3 years of relevant biotechnology or related industry experience, including Quality Control experience.Knowledge of GMP, SOPs, laboratory practices, and quality control processes.Experience with analytical techniques such as Flow Cytometry, ELISA, PCR/qPCR, or cell-based bioassays.Familiarity with OOS investigations, deviations, and root cause analysis.Preferred QualificationsExperience in the biotechnology or pharmaceutical industry. xzbcwsv Experience supporting analytical testing and biopharmaceutical product release.
Apply (by clicking the relevant button) after checking through all the related job information below.
Key ResponsibilitiesPerform analytical testing of raw materials, intermediates, and final products using techniques such as Flow Cytometry, ELISA, qPCR, and cell-based bioassays.Review laboratory data, test records, and documentation to support in-process testing and drug substance and drug product release.Assist with laboratory instrument calibration, routine maintenance, and laboratory readiness.Prepare and revise Standard Operating Procedures (SOPs), qualification and validation protocols, and reports.Support out-of-specification (OOS) investigations, deviations, and root cause analysis.Monitor compliance with GMP requirements, established procedures, and applicable quality systems.Review proposed changes to laboratory procedures, methods, and systems.Track laboratory metrics and support continuous improvement initiatives.Communicate testing updates and collaborate with scientific and technical teams.QualificationsBachelor’s degree; OR an associate degree with at least 2 years of relevant biotechnology or related industry experience, including Quality Control experience; OR a high school diploma with at least 3 years of relevant biotechnology or related industry experience, including Quality Control experience.Knowledge of GMP, SOPs, laboratory practices, and quality control processes.Experience with analytical techniques such as Flow Cytometry, ELISA, PCR/qPCR, or cell-based bioassays.Familiarity with OOS investigations, deviations, and root cause analysis.Preferred QualificationsExperience in the biotechnology or pharmaceutical industry. xzbcwsv Experience supporting analytical testing and biopharmaceutical product release.
Details
| Company | Infotree Global Solutions |
| Location | Frederick, Maryland, United States |
| Type | FULL TIME |
| Niche | hr |
| Experience | permanent |

