Quality Control Chemist - Biotech GMP, 12-Mo Onsite

Net2Source (N2S); Frederick (MD); On-site; USD 34,000 - 62,000; Full time

Job summary

Net2Source Inc. is seeking a Quality Control Chemist for a 12-month contract onsite.

The role requires performing testing of raw materials, intermediates and final products using analytical methods and QC procedures while maintaining laboratory equipment and ensuring compliant documentation for release. The candidate should have a degree in biotechnology or a related field with QC experience, knowledge of GMP and SOPs, and experience with analytical techniques such as flow cytometry, ELISA, and

Qualifications

• Bachelor's Degree or AA Degree with 2+ years' biotechnology or related field and Quality Control experience, OR High School Degree with 3+ years' biotechnology or related field and Quality Control experience.
• Requires hands-on QC experience in biotechnology or related field.
• Knowledge of GMP, SOPs and quality control processes.

Responsibilities

• Perform testing of raw materials, intermediates and final products by following analytical methods including flow cytometry, ELISA and qPCR assays.
• Maintain lab in optimal state and manage instrument calibration and routine maintenance.
• Assist with monitoring and trending data, review routine test data and related documents for in-process testing, drug substance and drug product release; generate CoAs for product release.

Skills

Quality control

Communication skills

Independent work

Education

Bachelor's/AA with QC experience

HS diploma with QC experience

Tools

MS Word

Excel

PowerPoint

Job description

Net2Source Inc. is seeking a Quality Control Chemist for a 12-month contract onsite.

The role requires performing testing of raw materials, intermediates and final products using analytical methods and QC procedures while maintaining laboratory equipment and ensuring compliant documentation for release. The candidate should have a degree in biotechnology or a related field with QC experience, knowledge of GMP and SOPs, and experience with analytical techniques such as flow cytometry, ELISA, and