Environmental Monitoring Technician

Job Title: Environmental Monitoring Technician

Job Description

The Environmental Monitoring (EM) Technician supports the Quality Control Microbiology team by performing routine environmental and utility monitoring within GMP-regulated cleanroom environments. This role helps maintain cleanroom integrity, ensures adherence to regulatory requirements, and contributes directly to overall product quality. You will join a team that is building out a new environmental monitoring program, giving you the opportunity to help shape new processes and contribute to a growing function.

Responsibilities

• Perform environmental monitoring of ISO-5, ISO-7, and ISO-8 cleanrooms, including viable air, non-viable particulate, and surface sampling in accordance with established procedures.
• Conduct utility sampling of systems such as WFI and RODI for bioburden and endotoxin testing to ensure water quality meets specifications.
• Execute personnel gowning monitoring and support gowning qualification programs to verify compliance with aseptic practices.
• Document all results accurately and completely in accordance with SOPs, cGMP, and GDP requirements.
• Monitor cleanroom conditions, including pressure differentials, on a routine basis to maintain proper environmental controls.
• Perform data entry, trending, and record maintenance for environmental monitoring activities, including analysis of EM data trends.
• Support investigations related to deviations, out-of-specification (OOS) results, and non-conformances by providing EM data and technical input.
• Prepare samples for internal and external laboratory testing, ensuring proper handling, labeling, and chain of custody.
• Assist in the sterilization and cleaning of laboratory equipment to support a controlled and compliant laboratory environment.
• Maintain inventory and manage the receipt of microbiological media and reagents to ensure continuous availability of supplies.
• Participate in environmental monitoring program improvements, audits, and compliance activities by contributing observations and suggestions.
• Collaborate cross-functionally with Quality Control, Quality Assurance, and Manufacturing teams to support production and quality initiatives.
• Support additional QC microbiology or laboratory tasks as needed, including microbial sampling and testing.
• Contribute to the build-out of a new environmental monitoring program and team by adopting new processes and supporting evolving team structures.

Essential Skills

• Hands-on experience with environmental monitoring (EM) sampling, including viable and non-viable monitoring.
• Practical knowledge of cleanroom operations in ISO 5–8 or Grade A–D environments.
• Proficiency in aseptic technique and personnel gowning procedures.
• Experience working under GMP, cGMP, and GDP requirements and following SOPs.
• Ability to perform microbiological testing such as bioburden, endotoxin, and TOC.
• Experience with surface, air, and personnel monitoring in controlled environments.
• Knowledge of water system sampling, including WFI and RODI systems.
• Capability to perform EM data trending and analysis to support investigations and continuous improvement.
• Strong laboratory documentation skills, including accurate data entry and technical writing.
• Experience supporting deviation, OOS, and CAPA activities through EM data and documentation.
• Between 1 and 6 years of experience in GMP, cleanroom, or environmental monitoring environments.
• Experience working in ISO 5–8 environments or aseptic processing settings.
• Familiarity with EM sampling techniques, including air sampling, water testing, bioburden testing, and microbial sampling.
• Understanding and application of aseptic technique in a quality control or microbiology laboratory setting.
• Associate’s or Bachelor’s degree in biology, microbiology, or a related scientific field.

Additional Skills & Qualifications

• Experience contributing to the development or expansion of an environmental monitoring program.
• Comfort working closely with Quality Control, Quality Assurance, and Manufacturing teams in a regulated setting.
• Ability to interpret and trend environmental monitoring data to identify patterns and support process improvements.
• Strong attention to detail and adherence to documentation standards in a cGMP environment.
• Effective communication skills for cross-functional collaboration and participation in audits and compliance activities.

Work Environment

This role is 100% onsite in a GMP-regulated facility with ISO 5–8 cleanroom environments and associated support areas. You will work primarily on the first shift, with a preferred start time of 8:00 a.m. or 9:00 a.m. to provide extended coverage into the late afternoon, and a standard 8-hour workday. The position involves frequent work inside controlled cleanrooms, routine monitoring of viable and non-viable particulates, and regular interaction with water systems such as WFI and RODI. You will use microbiological sampling tools, environmental monitoring equipment, and laboratory instruments while following aseptic technique and gowning procedures appropriate for cleanroom operations. The environment is highly regulated, detail-oriented, and collaborative, with close interaction among QC, QA, and Manufacturing teams as the organization builds and enhances a new environmental monitoring program.

This is a Contract position based out of Bedford, MA.

The pay range for this position is $22.00 - $30.00/hr.

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 Bedford,MA.

This position is anticipated to close on Jun 19, 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 process due to a disability, please email actalentaccommodation@actalentservices.com 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.

Salary : $22 - $30