Quality Control Chemist I - GMP QC & Bioassay Focus

R&D Partners; Frederick (MD); On-site; USD 50,000 - 63,000; Full time

Benefits offered by this job

Medical insurance - PPO

Employee Assistance Program

Long-term disability

Weekly payroll

Expense reimbursement

Job summary

R&D Partners in Frederick, MD is hiring a Quality Control Chemist I to perform testing of raw materials, intermediates and final products using cell-based bioassays, flow cytometry, ELISA and qPCR.

You will maintain the lab, review test data, and help generate CoAs for product release, while ensuring GMP and SOP compliance and supporting investigations of out-of-spec results. Competitive benefits and weekly payroll are offered.

Qualifications

• Bachelor's Degree or AA Degree with 2+ years' experience in biotechnology or related field and Quality Control experience
• High School Degree with 3+ years' experience in biotechnology or related field and Quality Control experience
• Strong knowledge of GMP, SOPs and quality control processes
• Identifying, writing, evaluating, and closing OOSs and investigations

Responsibilities

• Perform testing of raw materials, intermediates and final products by following analytical methods (cell-based bioassays, flow cytometry, ELISA and qPCR)
• Maintain lab equipment and ensure calibration/maintenance
• Review routine test data and related documents for in-process testing, drug substance and drug product release; support CoA generation
• Author or revise SOPs, qualification/validation protocols and reports
• Collaborate with internal/external resources to keep the lab in optimal condition

Skills

GMP knowledge

SOP understanding

Quality control

OOS investigations

Education

Bachelor's or Associate degree in biotech

High School degree with 3+ years' biotech QC experience

Job description

R&D Partners in Frederick, MD is hiring a Quality Control Chemist I to perform testing of raw materials, intermediates and final products using cell-based bioassays, flow cytometry, ELISA and qPCR.

You will maintain the lab, review test data, and help generate CoAs for product release, while ensuring GMP and SOP compliance and supporting investigations of out-of-spec results. Competitive benefits and weekly payroll are offered.