QC Cleanroom Analyst

Are you looking to advance your pharmaceutical career with a top-tier global life sciences leader? We are seeking a dedicated Quality Control Analyst to perform vital environmental monitoring across cleanroom environments in Ridgefield, NJ. If you thrive in aseptic manufacturing settings and prioritize cGMP excellence, this is the perfect opportunity to make an impact.

Location: Ridgefield, New Jersey
Job type: Contract
Work hours: 9 to 5

Responsibilities

• Perform daily viable and non-viable environmental monitoring (EM) in Grade A, B, C, and D cleanroom environments.
• Maintain logs and complete contemporaneous batch record documentation following strict ALCOA+ data integrity principles.
• Author and assist with out-of-specification (OOS) and non-conformance EM investigations.
• Review and revise EM Standard Operating Procedures (SOPs) and Batch Production Records (BPRs).
• Prepare daily plates, sanitize EM equipment, and assist manufacturing during periods of inactivity.

Requirements

• 2+ years of Quality Control experience within a pharmaceutical or biotechnology manufacturing facility.
• Hands-on experience with environmental monitoring in classified cleanroom environments (Grades A-D).
• Strong working knowledge of ALCOA+ principles and cGMP regulatory standards.
• Willingness to work a split shift (Sunday-Saturday) with mandatory overtime to support production schedules.

Skills

• Environmental Monitoring
• Quality Control (QC)

Pay

$25 - 30 per hour

Benefits

• Medical, prescription, dental, and vision insurance offerings
• AD&D and life insurance
• Short-term disability
• 401K plan (all benefits are based on eligibility)