Entry Level QC Role

Job Description

Job Description

Job Title: QC Scientist I, Nights Environmental Monitoring Job Description

The QC Scientist I, Nights Environmental Monitoring plays a key role in supporting sterile manufacturing operations by performing environmental monitoring activities within classified cleanrooms. This position focuses on routine and non-routine environmental sampling, accurate data processing and review, and ongoing assessment of cleanroom environmental conditions in alignment with Good Manufacturing Practices (GMPs), standard operating procedures, and site quality standards.

• Perform routine environmental monitoring sampling within classified cleanroom areas, including viable and non-viable monitoring activities, in accordance with approved procedures and established sampling plans.
• Collect, document, and process environmental monitoring samples and associated data accurately and in a timely manner.
• Review environmental monitoring results against established specifications, alert and action levels, and acceptance criteria, and identify and escalate excursions, atypical results, or other concerns according to applicable procedures.
• Perform data entry, calculations, data processing, and documentation within 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 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 appropriate.
• Collaborate effectively with Manufacturing, Quality Assurance, Microbiology, and other cross-functional groups to support manufacturing operations and maintain compliant cleanroom conditions.
• Complete required documentation and records accurately, contemporaneously, and in alignment with applicable procedures.
• Organize and manage assigned activities to meet established timelines and operational requirements in a fast-paced environment.
• 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.

• Ability to perform environmental monitoring sampling activities in classified cleanroom areas, including viable and non-viable monitoring, following detailed procedures and sampling instructions.
• Basic understanding of scientific principles and the ability to learn environmental monitoring techniques, cleanroom practices, and applicable GMP requirements.
• 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.
• Ability to perform basic mathematical calculations and data analysis.
• Ability to work effectively in a fast-paced manufacturing environment and manage assigned responsibilities while adapting to changing priorities.
• Ability to work independently within established procedures while recognizing when additional guidance or escalation is appropriate.
• Effective written and verbal communication skills and the ability to work collaboratively with cross-functional teams.
• Capability to comply with GMP, data integrity, and site quality standards in all monitoring and documentation activities.

• 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.
• 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.
• Familiarity with GMP principles and regulated laboratory or manufacturing environments.
• Demonstrated ability to follow standard operating procedures, sampling plans, and established cleanroom practices.

This contingent position operates within laboratory, manufacturing, and classified cleanroom areas on a SundaySaturday schedule, working night shifts. The role requires ordinary ambulatory skills and physical coordination sufficient to move throughout these areas, with the ability to stand and walk for prolonged periods and to periodically stoop, kneel, squat, crouch, bend, and reach while performing environmental monitoring and related activities. The position involves lifting, carrying, and moving light to medium weights of approximately 2550 pounds, with occasional pushing or pulling of heavier loads as required. It requires sufficient arm, hand, and finger dexterity to perform sampling, handle equipment and materials, and operate computers and instrumentation for extended periods. Visual acuity is needed to read procedures, labels, documentation, computer monitors, and instrumentation displays. The role also requires the ability to sit, reach with hands and arms, communicate, and hear for prolonged periods. Work is conducted in classified cleanroom environments while wearing required personal protective equipment and cleanroom garments for extended periods, following established gowning and aseptic practices. The environment is highly regulated and quality-focused, emphasizing safety, GMP compliance, collaboration with cross-functional teams, and support of sterile manufacturing operations.

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

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)

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

This position is anticipated to close on Oct 23, 2026.

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.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email View email address on ziprecruiter.com for other accommodation options.

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

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall 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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.