Environmental Monitoring Technician

Join a finished product pharmaceutical facility as an Environmental Monitoring Technician, where you will play a key role in maintaining the cleanliness and sterility of cleanroom environments. In this role, you support aseptic manufacturing operations through routine sanitization, environmental monitoring, and meticulous documentation, directly contributing to the production of life-changing therapies for people managing chronic conditions.

Responsibilities

• Perform routine sanitization of aseptic areas, including cleanrooms and associated equipment, following established procedures and standards.
• Conduct environmental monitoring to assess and document the cleanliness and sterility of controlled environments.
• Maintain the overall cleanliness and sterility of cleanroom environments, equipment, and support areas to comply with current Good Manufacturing Practices (GMP).
• Participate in event response activities and assist in deviation investigations as needed, providing observations and data to support root cause analysis.
• Record, review, and verify data in batch production records (BPRs) using Good Documentation Practices (GDP).
• Provide input and feedback on standard operating procedures (SOPs) and other controlled documents to support continuous improvement.
• Train peers in sanitization procedures, environmental monitoring techniques, and cross-functional systems to promote consistent and compliant practices.
• Follow all safety and environmental protocols in daily operations, including proper handling of sanitizing agents and use of personal protective equipment.
• Support process alignment and cleaning activities across aseptic core sanitization (direct), cartridge and vial filling lines (support), wash and sterilization (support), and formulation areas (support).
• Collaborate with manufacturing and quality teams to ensure aseptic standards are maintained and production schedules are supported.
• Adhere to all regulatory, quality, and site-specific requirements while working in a highly regulated manufacturing environment.

• Exposure to and understanding of Good Manufacturing Practices (GMP).
• Experience in a healthcare or previous manufacturing environment, preferably in a regulated setting (such as pharmaceutical, food, medical device, or cosmetics).
• Demonstrated interest in pharmaceutical manufacturing and working in a cleanroom environment.
• Previous housekeeping or sanitization experience in a professional setting.
• Ability to follow detailed SOPs and documentation requirements, including Good Documentation Practices (GDP).
• Strong attention to detail and commitment to cleanliness, sterility, and safety.
• Ability to work on your feet for extended periods, including 12-hour shifts in a manufacturing environment.
• Effective communication skills to collaborate with cross-functional teams and train peers.

• Bioworks training or an Associate’s degree in Biotechnology, demonstrating a strong desire to work in pharmaceutical manufacturing and initiative to learn more.
• Experience in a finished product manufacturing environment is a plus.
• Pharmaceutical manufacturing experience is a plus.
• Experience in other regulated industries such as food, medical device, or cosmetics is highly valued.
• Ability to adapt to a structured, highly regulated environment and follow strict procedures.
• Willingness to work night shifts and a rotating schedule.
• Motivation to grow and develop a long-term career in pharmaceutical manufacturing.

This role is based in a finished product pharmaceutical manufacturing facility with controlled cleanroom environments and aseptic areas. You will work primarily on night shifts following a 2-2-3 schedule, which typically involves working 12-hour shifts with a rotating pattern of on and off days. New hires generally train on day shift before transitioning to nights. The work requires being on your feet for extended periods and adhering to strict GMP, safety, and environmental protocols. You will work with sanitizing agents, cleanroom equipment, and production support systems in a highly regulated, team-oriented setting. The culture emphasizes diversity, inclusion, work-life balance, and career growth, offering opportunities to develop your skills and progress in various directions within pharmaceutical manufacturing.

Job Type & Location

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

The pay range for this position is $24.01 - $24.01/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 Clayton,NC.

This position is anticipated to close on Jun 3, 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 : $24