Senior Quality Control Associate - Chemistry

Location: West Greenwich, RI – 100% on-site role

Position Type: 12-month contract

About the role

The Senior Quality Control Associate – Chemistry will work on-site at the client’s Rhode Island facility under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing in-process, release, and stability samples using sophisticated equipment and methodologies.

Responsibilities

• 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
• Ensure that facilities, equipment, materials, organization, processes, procedures, and products follow cGMP practices and other applicable regulations
• Operate laboratory equipment and instrumentation, including HPLC/UPLC, capillary electrophoresis, and general chemistry methodologies (Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing)
• Perform review and approval of assays, documents, and records
• Support Continual Improvement initiatives
• Alert management of quality, compliance, supply, and safety risks
• Participate in laboratory investigations
• Perform general laboratory housekeeping activities
• Complete required assigned training to permit carry-through of required tasks
• Perform additional duties as specified by management

Requirements

• High school diploma or GED with 2 years' work experience; OR Associate's degree with 6 months' work experience; OR Bachelor's degree
• Minimum 2 years' work experience (or equivalent education per Basic Qualifications above)
• Must be authorized to work for ANY employer in the U.S. (no visa sponsorship available)

Skills

• Required: HPLC (High-Performance Liquid Chromatography), Quality Control experience, Laboratory chemistry experience
• Preferred:
  • 1–2 years' experience in HPLC/UPLC, capillary electrophoresis, and general chemistry methodologies (Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing)
  • Demonstrated experience in laboratory investigations, method validation, audits, and QC processes
  • Proven ability to interpret scientific data
  • Self-motivated, with strong organizational skills and ability to manage multiple tasks with minimal direction

Pay

$21.00–$24.00 / hour (USD)

Schedule

Standard 8:00 AM – 5:00 PM local hours

Benefits

• Medical, Vision, and Dental Insurance Plans
• 401k Retirement Fund