Environmental Monitoring Technicians

We are seeking a detail-oriented Environmental Monitoring (EM) Analyst to support our Manufacturing & Supply Division in delivering high-quality biopharmaceutical products to patients worldwide. This role sits within Quality Operations and plays a critical part in maintaining compliance, ensuring product safety, and supporting a reliable global manufacturing network. The EM Analyst will execute environmental and utility monitoring activities in a GMP-regulated environment and partner closely with manufacturing and quality teams to uphold rigorous regulatory standards.

Responsibilities

• Maintain and execute the Environmental Monitoring (EM) program in accordance with GMP requirements
• Perform environmental sampling in classified areas, including active air, surface, and non-viable air sampling
• Collect and test qualified utility systems such as Clean Steam, WFI, and compressed gases
• Perform routine personnel monitoring and sample accountability activities (weekly and monthly)
• Read EM plates and conduct TOC, conductivity, and gas testing
• Enter, review, and approve data within LIMS and other quality systems
• Compile, trend, and evaluate environmental data to identify adverse trends
• Support Performance Qualification (PQ) and re-qualification activities
• Author and summarize protocols, special studies, and annual reviews
• Support investigations and equipment calibration, documentation control, and other duties as assigned by management

Education

• Associate’s degree in a science-related field (required)
• Bachelor’s degree in Biological Sciences (preferred)

Experience

• Minimum of 1 year post-degree experience in Environmental Monitoring, Aseptic Manufacturing, or Microbiological Laboratory Operations
• Basic understanding of GMPs and regulatory requirements for sterile pharmaceutical or vaccine manufacturing
• Strong attention to detail, flexibility, and awareness of production and quality control challenges
• Demonstrated oral and written communication skills
• Ability to sit, stand, and move within the workspace for extended periods
• Ability to perform repetitive tasks and lift up to 50 pounds

Preferred Experience:

• Environmental Monitoring sampling in a GMP pharmaceutical setting (non-EPA)
• Quality Control, Quality Assurance, and/or cGMP experience
• Experience using GLIMS, LIMS, SAP, TrackWise, or similar systems

Additional Information

• Shift: Wednesday–Saturday, 4:00 PM–2:30 AM EST (4 × 10-hour shifts)
• Training Period:
• Duration: 8–12 weeks
• Schedule may vary (day shift 8:00 AM–5:00 PM EST or evening shift 4:00 PM–10:00 PM EST, Monday–Friday)

Pre-Employment Requirements:

• Varicella titer and BCG screening required prior to start date
• Dress Code & Workplace Requirements:
• Business casual attire required
• No athletic/workout clothing
• No makeup, eyelash extensions, jewelry, long nails, or nail polish
• Adherence to Merck safety guidelines and time-off request policies is mandatory