QC Scientist I, Nights B

Job Title: QC Scientist I, Environmental Monitoring (Night Shift) Job Description
The QC Scientist I, Environmental Monitoring, supports sterile manufacturing operations by performing environmental monitoring activities in classified cleanrooms during night shifts. This role focuses on executing routine and non-routine environmental sampling, processing and reviewing data, and assessing cleanroom environmental conditions in alignment with Good Manufacturing Practices (GMPs), standard operating procedures, and site quality standards. The position is ideal for individuals with a strong attention to detail, an interest in cleanroom and aseptic operations, and the ability to work effectively in a fast-paced, regulated environment.
Responsibilities
- Perform routine environmental monitoring sampling within classified cleanroom areas, including viable and non-viable monitoring, in accordance with approved procedures and established sampling plans.
- Collect, document, and process environmental monitoring samples and associated data accurately and within required timeframes.
- Review environmental monitoring results against established specifications, alert and action levels, and acceptance criteria, and identify and escalate excursions, atypical results, or other concerns following applicable procedures.
- Perform data entry, calculations, data processing, and documentation in applicable laboratory and environmental monitoring databases and systems.
- Support the review and evaluation of environmental monitoring data to assess the ongoing state of control of classified cleanrooms.
- Provide environmental monitoring oversight of assigned classified areas by observing environmental conditions, identifying potential issues, and communicating observations or concerns to appropriate personnel.
- Support investigations related to environmental monitoring excursions, deviations, and other events by providing accurate data, documentation, and technical input as appropriate.
- Maintain a thorough understanding of applicable SOPs, sampling procedures, GMP requirements, and environmental monitoring program expectations.
- Ensure that all environmental monitoring activities and associated documentation comply with GMP requirements, data integrity principles, and site procedures.
- Operate and maintain environmental monitoring equipment and supplies in accordance with applicable procedures, and identify and escalate equipment or procedural issues as needed.
- Collaborate effectively with Manufacturing, Quality Assurance, Microbiology, and other cross-functional groups to support manufacturing operations and maintain compliant cleanroom conditions.
- Complete all required documentation and records accurately, contemporaneously, and in accordance with applicable procedures.
- Organize and manage assigned activities to meet established timelines and operational requirements.
- Complete all required safety, quality, GMP, and job-specific training.
- Follow applicable safety requirements and established cleanroom gowning and aseptic practices while performing assigned activities.
- Perform additional duties and responsibilities as assigned by area supervision or designee.
Essential Skills
- Bachelors degree in Biology, Microbiology, Biochemistry, or a related scientific discipline is preferred; an equivalent combination of education, training, and relevant experience will be considered.
- Basic understanding of scientific principles and the ability to learn environmental monitoring techniques, cleanroom practices, and applicable GMP requirements.
- Ability to accurately follow detailed procedures, sampling instructions, and established practices in a regulated environment.
- Strong attention to detail with a commitment to accurate, complete, and timely documentation.
- Strong organizational, problem-solving, and critical-thinking skills.
- Ability to review data, recognize atypical results or conditions, and appropriately communicate and escalate potential issues.
- Proficiency with Microsoft Office applications, including Excel and Word.
- Effective written and verbal communication skills.
- Ability to work collaboratively with cross-functional teams such as Manufacturing, Quality Assurance, and Microbiology.
- Ability to work effectively in a fast-paced manufacturing environment and manage assigned responsibilities.
- Ability to adapt to changing priorities while maintaining high quality and compliance standards.
- Ability to perform basic mathematical calculations and data analysis.
- Ability to work independently within established procedures while recognizing when to seek additional guidance or escalate issues.
Additional Skills & Qualifications
- Previous experience in environmental monitoring, cleanroom operations, aseptic manufacturing, pharmaceutical manufacturing, or another regulated environment is preferred but not required.
- Experience with laboratory information management systems (LIMS), environmental monitoring systems, or similar databases is a plus.
- Comfort working with electronic databases and documentation systems in a GMP environment.
- Demonstrated reliability in meeting timelines and operational commitments.
- Willingness to work night shifts and a flexible schedule within a SundaySaturday operation.
- Physical ability to meet the demands of the role, including standing and walking for prolonged periods; periodically stooping, kneeling, squatting, crouching, bending, and reaching while performing environmental monitoring and related activities.
- Ability to lift, carry, and move light to medium weights of approximately 2550 pounds, with occasional pushing or pulling of heavier loads as required.
- Sufficient arm, hand, and finger dexterity to perform sampling activities, handle equipment and materials, and operate computers and instrumentation for extended periods.
- Visual acuity sufficient to read procedures, labels, documentation, computer monitors, and instrumentation displays.
- Ability to sit, reach with hands and arms, communicate, and hear for prolonged periods as required by the role.
Work Environment
This contingent position operates within a regulated pharmaceutical manufacturing setting in the United States, supporting sterile operations on a night shift schedule within a SundaySaturday operation. The QC Scientist I works primarily in classified cleanroom environments, laboratories, and manufacturing areas, routinely moving throughout these spaces to perform environmental monitoring activities. The role requires wearing appropriate personal protective equipment (PPE) and full cleanroom garments for extended periods, following strict gowning and aseptic practices. Work involves frequent use of environmental monitoring equipment, computers, instrumentation, and electronic databases, including laboratory and environmental monitoring systems. The environment is fast paced and highly quality-focused, with close collaboration across Manufacturing, Quality Assurance, Microbiology, and other functional groups. The position demands consistent adherence to GMP, data integrity, and safety requirements while maintaining comfort with extended standing, walking, and physical activity in a controlled cleanroom setting.
Job Type & Location
This is a Contract position based out of Greenville, NC.
Pay and Benefits
The pay range for this position is $26.00 - $27.00/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)
Job Type & Location
This is a Contract position based out of Greenville, NC.
Application Deadline
This position is anticipated to close on Oct 22, 2026.
Workplace Type
This is a fully onsite position in Greenville,NC. 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.

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Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
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