QC Analyst - Potency
Listed on 2026-09-25
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Data Analyst, QA Specialist - Analyst/Manager
Job Title: QC Analyst - Potency
Location: Rockville, MD
Type: Contract
Schedule: Monday
- Friday 8am-5pm
Overview
Biopharmaceutical Company is seeking a QC Analyst to join their team in Rockville, MD!
Responsibilities
- Perform testing and analysis of potency samples in accordance with established protocols and Good Manufacturing Practices (GMP).
- Ensure accurate documentation of test results and maintain thorough records for compliance and audit purposes.
- Operate laboratory instrumentation such as HPLC, spectrophotometers, and other analytical tools to assess sample quality.
- Interpret data, prepare reports, and communicate findings to cross-functional teams.
- Maintain a clean, organized, and compliant lab environment, adhering to safety standards and company policies.
- Collaborate with quality assurance and manufacturing teams to support product release and stability studies.
Job Title: QC Analyst
- Potency
Location: Rockville, MD
Type: Contract
Schedule: Monday - Friday 8am-5pm
Overview
Biopharmaceutical Company is seeking a QC Analyst to join their team in Rockville, MD!
Responsibilities
- Perform testing and analysis of potency samples in accordance with established protocols and Good Manufacturing Practices (GMP).
- Ensure accurate documentation of test results and maintain thorough records for compliance and audit purposes.
- Operate laboratory instrumentation such as HPLC, spectrophotometers, and other analytical tools to assess sample quality.
- Interpret data, prepare reports, and communicate findings to cross-functional teams.
- Maintain a clean, organized, and compliant lab environment, adhering to safety standards and company policies.
- Collaborate with quality assurance and manufacturing teams to support product release and stability studies.
- Bachelor’s degree in Chemistry, Biology, Biochemistry, or a related scientific field.
- 4-5 years of experience in GMP environment performing ELISA's, MSD, and bioassays for potency residuals within a biotech company.
- Experience with good documentation practices required. (may consider CLIA or GLP experience if candidates do not have GMP)
System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M-3
: #558-Scientific
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).