QA Auditor

Job Title: QA Auditor

Job Description

The QA Auditor role involves comprehensive in-house line audits of pharmaceutical filling and packaging operations, ensuring compliance with SOPs, performing line clearances, in-process, and end-item inspections. Responsibilities include reviewing and applying specifications for the acceptance of incoming packaging components, raw materials, and finished products, generating, reviewing, and issuing batch production records, releasing materials and components for production, organizing and distributing printed materials to production, and monitoring and interpreting charts and gauges. Successful candidates are expected to have knowledge of contemporary cGMP practices and procedures, with excellent written and oral communication skills.

Responsibilities

• Conduct in-house line audits of pharmaceutical filling and packaging operations.
• Review manufacturing activities and documentation for SOP compliance.
• Perform line clearances, in-process, and end-item inspections.
• Review and apply specifications for acceptance of packaging components, raw materials, and finished products.
• Generate, review, and issue batch production records.
• Release materials and components for production use.
• Organize and issue printed materials to production.
• Monitor and interpret charts and gauges.
• Perform log book review, issuance, and archival.

Essential Skills

• Quality assurance
• Audit
• Internal audit
• Auditing
• Compliance
• Inspection
• Knowledge of micrometers and calipers
• Quality control
• Quality inspection

Additional Skills & Qualifications

• Associates degree in Science or equivalent required.
• Bachelor's degree in Science or equivalent preferred.
• 1-4 years experience in Quality Assurance or Manufacturing, preferably in an FDA regulated environment.
• Working knowledge of cGMPs preferred.
• Technical writing skills are a plus.

Work Environment

The work environment includes clean rooms, manufacturing, and lab settings. The typical schedule is the first shift, consisting of four 10-hour days, with standard hours from 6:00 AM to 4:30 PM. Availability for various days of the week and a 5-day schedule is required. Overtime rates apply to hours over 40 per week. Alternative work hours or schedules may be required at management's discretion.

This is a Permanent position based out of Syracuse, NY.

The pay range for this position is $43680.00 - $52000.00/yr.

Company Benefits • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Syracuse,NY.

This position is anticipated to close on Feb 16, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $43,680 - $52,000