Quality Control Senior Associate

Quality Control Senior Associate Spectraforce Technologies United States, Rhode Island, West Greenwich Apr 21, 2026

Job Title:

Quality Control Senior Associate Location:

West Greenwich, Rhode Island Duration:

12

Months Shift:

Standard 8-5 local hours

Description:

The role will be on-site based out of Client Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing the following: in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing.

Responsibilities include the following:

Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations Operate laboratory equipment and instrumentation Performs review and approval of assays, documents and records Supports Continual Improvement initiatives Alerts management of quality, compliance, supply and safety risks Participate in laboratory investigations Perform general laboratory housekeeping activities Completes required assigned training to permit carry through of required tasks Performs additional duties as specified by management Basic Qualifications Master's Degree Bachelor's Degree and 2 years of Quality experience Associate's degree and 6 years of Quality experience High school diploma/GED and 8 years of Quality experience Preferred Qualifications 1-2 years' experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing Demonstrated experience in laboratory investigations, method validation, audits, QC processes Proven ability to interpret scientific data Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction Basic Qualifications High school/GED + 2 years work experience OR? Associates and 6 months work experience OR? Bachelors Top 3

Must Have Skill Sets:

HPLC, General Chem, CE Day to

Day Responsibilities:

GMP Testing, Performs review and approval of assays, Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks.

Possible Extension:

Yes Red Flags:

No QC past experience

Interview Process:

1 Stage of interview only | MS Teams. Interview with 2-4 panelist