Quality Control Analyst – Potency

Job overview

The Quality Control Analyst – Potency role is onsite in Rockville, MD; compensation is not specified. The analyst will join a biopharmaceutical company’s quality control team, with System One providing workforce solutions and outsourced services.

What you'll do

• Test and analyze potency samples under established protocols and GMP
• document results and maintain compliance records
• operate HPLC, spectrophotometers, and other analytical instruments
• interpret data and report findings
• maintain a compliant laboratory
• and collaborate with quality assurance and manufacturing teams on product release and stability studies.

What we're looking for

Skills & competencies

quality control analyst

potency

rockville md

system one

biopharmaceutical

laboratory testing

hplc

gmp

monday–friday

8 a.m.–5 p.m.

quality assurance

product release

Work arrangement

• Weekend coverage required

Benefits & perks

• Eligible employees may have medical, dental, vision, spending account, life insurance, voluntary plan, and 401(k) options.

Why this role

The posting lists a Monday–Friday, 8 a.m.–5 p.m. schedule and contract type. A bachelor’s degree in a related scientific field and prior QC experience are requested; HPLC proficiency and GMP knowledge are specified.

About the employer

System One is hiring for this role. Industry: Temporary Help Services. Sector: 56.