Quality Control Analyst III (Pharmaceutical QC)

Location: Rensselaer, New York, United States; onsite laboratory role.

Salary: $92,000 per year

Company

hirify.global provides staffing and employment services for technical and scientific roles.

What you will do

• Perform analytical testing for incoming, in-process, raw material, final product, and stability samples.
• Conduct liquid and gas chromatography after qualification and training, along with wet chemistry assays.
• Collect water samples and maintain laboratory equipment, instruments, and calibration records.
• Prepare the laboratory for audits and support laboratory housekeeping.
• Review QC data, prepare summaries for management, and assist with OOS, deviation, and CAPA investigations.
• Manage QC sample receipt, testing logistics, shipment tracking, result distribution, and closure as a backup.

Requirements

• Bachelor’s degree in Chemistry or a related field.
• 5+ years of pharmaceutical QC experience with APIs or finished dosages.
• Working knowledge of GC and HPLC.
• Knowledge of FDA GMP requirements, including 21 CFR Parts 211, 820, and/or 600.
• Strong communication, analytical, organizational, mathematical, and technical writing skills.
• Proficiency with Microsoft Office Suite and instrument manufacturer software; ability to work onsite and meet physical laboratory requirements, including lifting up to 50 pounds.

Nice to have

• Knowledge of ISO 9001 and ISO 13485.

Culture & Benefits

• Temporary assignments lasting 13 weeks or longer may include major medical, dental, vision, and 401(k) benefits.
• Statutory sick pay is provided where required.
• Reasonable accommodations are available throughout the employment process.
• Equal opportunity employment and participation in E-Verify in certain locations.