QC Chemist I

Zohorecruit; Frederick (MD); On-site; USD 36,000 - 47,000; Part time

Benefits offered by this job

Medical

Paid Sickleave

401K

Job summary

Zohorecruit seeks a QC Chemist I based in Frederick, MD to perform testing of raw materials, intermediates and final products using diverse analytical methods, ensuring GMP compliance and data integrity.

The role is a long-term contract with potential conversion to full-time. Pay is $30/hr on W2, with Medical, Paid Sick Leave and 401K benefits. Degree options include Bachelor’s, AA or high school.

Qualifications

• Bachelor’s, associate or high school degree accepted.

Responsibilities

• Test materials and final products using cell-based bioassays, flow cytometry, ELISA and qPCR.
• Coordinate with internal/external resources to keep the lab in an optimal state.
• Review test data and related documents for in-process testing, drug substance and drug product release; provide CoAs.
• Maintain laboratory instruments with calibration and routine maintenance.
• Author or revise SOPs, qualification/validation protocols and reports.
• Monitor GMP systems to ensure compliance with policies.

Education

Bachelor’s Degree OR AA Degree OR High School Degree

Tools

Flow Cytometry

ELISA

PCR

Cell bioassays

Job description

Frederick, United States | Posted on 09/30/2026

QC ChemistI based in Frederick, MD

Our client, a worldleader in life sciences and biotechnology, is looking for a QC ChemistI based in Frederick, MD.

Job Duration:LongTerm Contract(Possibility of Conversion to FTE)

Pay Rate : $30/hr on W2

Company Benefits

• Medical
• Paid Sickleave
• 401K

Key Responsibilities

• Performtesting of raw materials, intermediates and final products by followinganalytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCRassays.
• Workwith internal and external resources to maintain lab in an optimal state.
• Assistwith monitoring and trending data, complete routine record review of testdata and related documents for in-process testing, drug substance and drugproduct release. Supply information to support generation of CoAs forproduct release.
• Maintainslaboratory instruments for calibration and routine maintenance
• Authoror revise SOPs, qualification/validation protocols and reports.
• Monitorthe GMP systems currently in place to ensure compliance with documentedpolicies.

Qualifications

• Bachelor’s Degree OR AADegree OR High School Degree

PreferredQualifications

• Strong knowledge ofGMP, SOPs and quality control processes.
• Identifying, writing,evaluating, and closing OOS’s and investigations.
• Well versed in variousanalytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassaysand other applicable methods to the testing of biopharmaceuticals.
• Working knowledge ofquality systems and regulatory requirements (21 CRF Part 11/210/211).