Quality Control Chemist - I
Unicon Pharma Inc · Frederick, Maryland, United States
FULL TIMEpermanent
Job Description
Job Title: Quality Control ChemistLocation: Frederick, MD (Onsite)Shift: Wednesday–Saturday, 3:00 PM–1:30 AM ESTNote: First 7 weeks require Monday–Friday, 7:30 AM–4:00 PM for onboarding and training.
Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.
Key Responsibilities:Perform QC testing of raw materials, intermediates, and finished products using Flow Cytometry, ELISA, qPCR, and cell-based bioassays.Review and trend test data, maintain GMP documentation, and support product release and Certificates of Analysis (CoAs).Maintain lab instruments, calibration, and routine maintenance.Write and revise SOPs, validation protocols, and reports.Support OOS investigations, deviations, and root cause analysis.Ensure GMP compliance, review procedural changes, and support continuous improvement.
Basic Qualifications:Bachelor’s degree; OR Associate degree with 2+ years of relevant biotechnology and QC experience; OR High school diploma with 3+ years of relevant experience.
Preferred Qualifications:Strong knowledge of GMP, SOPs, QC processes, and OOS investigations.Hands-on experience with Flow Cytometry, ELISA, PCR/qPCR, and cell-based assays.Knowledge of regulatory requirements (21 CFR Parts 11, 210, and 211).Proficiency in MS Office and strong communication skills. xzbcwsv Preferred experience in the biotechnology or pharmaceutical industry.
Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.
Key Responsibilities:Perform QC testing of raw materials, intermediates, and finished products using Flow Cytometry, ELISA, qPCR, and cell-based bioassays.Review and trend test data, maintain GMP documentation, and support product release and Certificates of Analysis (CoAs).Maintain lab instruments, calibration, and routine maintenance.Write and revise SOPs, validation protocols, and reports.Support OOS investigations, deviations, and root cause analysis.Ensure GMP compliance, review procedural changes, and support continuous improvement.
Basic Qualifications:Bachelor’s degree; OR Associate degree with 2+ years of relevant biotechnology and QC experience; OR High school diploma with 3+ years of relevant experience.
Preferred Qualifications:Strong knowledge of GMP, SOPs, QC processes, and OOS investigations.Hands-on experience with Flow Cytometry, ELISA, PCR/qPCR, and cell-based assays.Knowledge of regulatory requirements (21 CFR Parts 11, 210, and 211).Proficiency in MS Office and strong communication skills. xzbcwsv Preferred experience in the biotechnology or pharmaceutical industry.
Details
| Company | Unicon Pharma Inc |
| Location | Frederick, Maryland, United States |
| Type | FULL TIME |
| Niche | hr |
| Experience | permanent |