QC Environmental Monitoring Technician (QC EM Tech)

Job Title: QC Environmental Monitoring Technician (QC EM Tech)

Shift: Nights after training - Must be flexible to train for 3 months on 1st (8am-5pm), 2nd (2pm-11pm) and later move to night shift (6pm-6am)

Job Description

The QC Environmental Monitoring Technician performs critical environmental and utility monitoring in controlled manufacturing areas to support the production of high-quality biopharmaceutical products. This role involves routine sampling, laboratory support activities, accurate documentation, and adherence to regulatory and company standards. It is an excellent opportunity for early-career professionals with laboratory experience who want to develop their skills in a highly regulated, fast-paced environment.

Responsibilities

• Perform environmental monitoring in controlled and classified manufacturing areas, including surface monitoring, viable air monitoring, and non-viable particulate monitoring.
• Conduct personnel monitoring as required to support aseptic manufacturing operations.
• Perform sampling of critical utilities such as feed water, reverse osmosis (RO) water, water-for-injection (WFI), pure steam, and compressed gases.
• Operate within aseptic and controlled environments while following established environmental monitoring procedures and standards.
• Complete autoclaving of laboratory supplies to ensure proper sterilization and readiness for use.
• Carry out general laboratory maintenance duties to support a clean, organized, and compliant work area.
• Gown appropriately and consistently to enter various classified manufacturing areas, following established gowning procedures.
• Perform accurate and timely record keeping, both manually and electronically, in accordance with company policies and regulatory requirements.
• Use computer systems, including Microsoft Office and other electronic systems, to document results, maintain logs, and support quality and compliance activities.
• Follow all applicable standard operating procedures (SOPs), good manufacturing practices (GMP), and safety guidelines while performing daily tasks.
• Troubleshoot routine issues related to environmental monitoring activities and laboratory processes within established guidelines.
• Adapt to changing schedules, priorities, and operational needs while maintaining a high level of attention to detail and quality.

Essential Skills

• Laboratory experience in a scientific or technical setting.
• Experience or familiarity with environmental monitoring or laboratory operations.
• Basic understanding of aseptic techniques and aseptic manufacturing operations, or willingness to learn in a regulated environment.
• Proficiency with computer systems, including Microsoft Office applications.
• Ability to accurately complete manual and electronic documentation in compliance with company and regulatory standards.
• Capability to follow detailed procedures, SOPs, and regulatory requirements in a GMP or similarly regulated environment.
• Strong attention to detail and commitment to data integrity and quality.
• Flexibility to work 12-hour shifts and adapt to rotating schedules, including weekends.
• Ability to gown and work for extended periods in controlled, classified manufacturing and laboratory environments.

Additional Skills & Qualifications

• Prior experience in the biopharmaceutical or pharmaceutical industry is preferred.
• Prior environmental monitoring (EM) experience and/or laboratory experience is preferred.
• Knowledge of aseptic manufacturing operations is highly beneficial.
• Degree in a related science field is preferred; substantial environmental monitoring experience may be considered in lieu of a degree.
• Troubleshooting skills related to laboratory or environmental monitoring activities.
• Strong adaptability and comfort with change in a dynamic production environment.
• Motivation to learn and grow within a long-term, career-building opportunity.

Work Environment

This position is 100% on-site in a laboratory and manufacturing environment that includes controlled and classified cleanroom areas. The role involves working three 12-hour shifts per week, either 6:00 a.m. to 6:00 p.m. or 6:00 p.m. to 6:00 a.m., typically on a Sun–Wed or Thurs–Sat schedule. Initial training will be on day shift for approximately 2–3 months, generally five days per week with rotating Saturdays, before transitioning to the permanent 12-hour shift schedule. You will work extensively in lab and cleanroom settings, performing environmental and utility monitoring, handling autoclaved supplies, and following strict aseptic and safety procedures. Gowning into various manufacturing areas is required and includes wearing appropriate cleanroom attire for extended periods. The environment is fast-paced and highly regulated, with a strong focus on quality, compliance, and teamwork. The position is offered as a long-term contract with the expectation of renewals, and includes benefits such as accrued paid time off, paid holidays, and medical, dental, and vision coverage.

This is a Contract position based out of La Verne, CA.

The pay range for this position is $23.00 - $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 La Verne,CA.

This position is anticipated to close on Apr 20, 2026.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

About Actalent

Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.