Environmental Monitoring Analyst

The Environmental Monitoring Analyst performs routine environmental monitoring across manufacturing and laboratory areas to support contamination control and product quality. This role focuses on collecting and processing viable and non-viable samples from manufacturing and utility systems, documenting results in electronic systems, and following Good Manufacturing Practices (GMP) and standard operating procedures. It offers an excellent entry point into the pharmaceutical and life sciences industry, with strong training, mentorship, and opportunities for long-term growth into microbiology, quality, and laboratory-focused roles.

• Perform routine environmental monitoring sampling throughout the manufacturing facility, including controlled manufacturing spaces and laboratory areas.
• Collect viable and non-viable samples from manufacturing and utility systems, including compressed gas systems and water systems such as WFI.
• Incubate environmental monitoring plates, read and interpret results, and document findings accurately within electronic documentation systems.
• Follow GMP procedures and site standard operating procedures to ensure compliance with contamination control and qualification activities.
• Support monitoring activities for facility environments, compressed gas systems, water systems, and controlled manufacturing spaces to maintain a state of control.
• Maintain accurate, timely, and complete documentation and records in a paperless environment, adhering to data integrity standards.
• Participate in routine operational and compliance activities related to environmental monitoring and quality systems.
• Apply aseptic techniques during sampling and handling of materials to minimize contamination risks.
• Collaborate with cross-functional teams in manufacturing, quality, and laboratory operations while also working independently when required.
• Communicate clearly and professionally about monitoring results, deviations, and observations to relevant stakeholders.
• Demonstrate strong attention to detail in sample collection, plate reading, data entry, and documentation review.
• Adapt to changing schedules, priorities, and environments while maintaining high standards of quality and compliance.
• Engage in ongoing training and mentorship activities to build expertise in environmental monitoring, microbiology, GMP operations, and quality systems.

• Bachelor's degree in Biology, Microbiology, Pharmaceutical Sciences, Environmental Science, Chemistry, or a related scientific field.
• Foundational knowledge of microbiology and laboratory practices.
• Understanding of aseptic technique and contamination control principles.
• Strong communication skills, both written and verbal, for documenting results and collaborating with team members.
• Strong organizational skills with the ability to manage multiple monitoring activities and documentation requirements.
• Ability to work independently with minimal supervision while also contributing effectively within a team environment.
• Demonstrated attention to detail in sampling, plate reading, and electronic documentation.
• Willingness to learn and develop new skills in environmental monitoring, GMP operations, and quality systems.
• Agility in adapting to changing environments, schedules, and operational priorities.
• Comfort using electronic documentation systems in a paperless environment.

• Experience in GMP manufacturing environments is preferred.
• Experience in pharmaceutical or biotechnology settings is preferred.
• Experience in laboratory operations, including handling and processing samples, is preferred.
• Experience in environmental monitoring activities is preferred.
• Experience in microbiology, including plate incubation and reading, is preferred.
• Familiarity with LIMS or other electronic documentation and data management systems is preferred.
• Exposure to bioworks or similar technical training programs is beneficial.
• Interest in long-term career growth into microbiology, quality, and laboratory-based roles within the life sciences industry.

This role operates in both manufacturing and laboratory environments that follow GMP and contamination control standards. The position requires the ability to stand and walk for extended periods while performing sampling and monitoring activities throughout the facility. The analyst must be able to lift up to 35 pounds as part of routine duties, such as handling equipment and materials. Work hours are Monday through Friday, approximately 8:00 AM to 4:30 PM, with a mandatory team meeting at 8:15 AM each day. The environment emphasizes safety, quality, collaboration, and professional development, supported by a strong training program and mentorship to help team members grow within a leading life sciences organization.

This is a Contract position based out of Sanford, NC.

The pay range for this position is $25.00 - $25.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • 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 Sanford,NC.

This position is anticipated to close on Aug 27, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.