
QC Scientist I Nights B
Greenville, NCContractup to $27/hrSeen 1 day agoSeen in employer's feed 1 day ago
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Job overview
The QC Scientist I – Environmental Monitoring role supports sterile manufacturing in a GMP‑regulated pharmaceutical facility, performing routine and non‑routine monitoring of cleanroom environments, documenting results, and collaborating with quality, microbiology, and manufacturing teams to maintain compliance.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
QC Scientist I – Environmental Monitoring
Location: Greenville, NC
Schedule: B Shift | 2-2-3 Schedule | 6:00 PM–6:00 AM
Pay: Up to $27/hour , based on experience
Employment Type: Contract-to-Hire
Contract Duration: Through October 13, 2027 , with potential for continued employment based on performance and business needs
Work Arrangement: Fully Onsite
Opportunity
We are seeking a QC Scientist I – Environmental Monitoring to join a pharmaceutical manufacturing environment in Greenville, NC. This is an excellent opportunity for a scientist who wants hands-on experience supporting sterile manufacturing, classified cleanrooms, Environmental Monitoring, and GMP-regulated operations .
The successful candidate will perform routine and non-routine Environmental Monitoring activities, document and review results, identify potential excursions or atypical findings, and work closely with Quality, Microbiology, Manufacturing, and other cross-functional teams to help maintain compliant cleanroom conditions.
This position is contract-to-hire , with the current assignment running through October 13, 2027 and the potential for continued employment depending on performance, business needs, and available opportunities.
What You'll Do
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Perform routine Environmental Monitoring activities within classified cleanroom areas supporting sterile manufacturing.
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Conduct viable and non-viable environmental sampling according to approved procedures and established sampling plans.
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Accurately collect, document, process, and enter Environmental Monitoring samples and associated data.
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Review results against established specifications, alert/action levels, and acceptance criteria.
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Identify and appropriately communicate or escalate excursions, atypical results, or potential environmental concerns .
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Perform data entry, calculations, data processing, and documentation using applicable laboratory and Environmental Monitoring systems.
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Support the evaluation of Environmental Monitoring data to help assess the ongoing state of control of classified cleanrooms.
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Provide Environmental Monitoring oversight of assigned areas and communicate observations or concerns to appropriate personnel.
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Support investigations related to Environmental Monitoring excursions, deviations, and other quality events by providing accurate documentation and technical information.
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Operate and maintain Environmental Monitoring equipment and supplies according to established procedures.
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Partner with Quality Assurance, Microbiology, Manufacturing, and other cross-functional teams to support manufacturing operations.
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Maintain accurate, timely, and compliant documentation in accordance with GMP and data integrity requirements.
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Follow established cleanroom gowning, aseptic practices, safety requirements, SOPs, and GMP procedures.
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Complete required training and maintain compliance with site quality and safety expectations.
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Manage assigned responsibilities and timelines in a fast-paced manufacturing environment.
What We're Looking For
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Bachelor's degree in Biology, Microbiology, Biochemistry, or a related scientific discipline preferred.
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Equivalent combination of education, training, and relevant experience will be considered.
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Previous experience in Environmental Monitoring, cleanroom operations, aseptic processing, pharmaceutical manufacturing, microbiology, or another regulated environment is preferred but not required.
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Strong attention to detail and commitment to accurate documentation.
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Ability to follow detailed procedures and work within a highly regulated environment.
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Ability to review data, recognize unusual results or conditions, and appropriately escalate concerns.
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Basic scientific, mathematical, and data-analysis skills.
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Strong organizational and problem-solving abilities.
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Working knowledge of Microsoft Office, particularly Excel and Word .
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Experience with LIMS, Environmental Monitoring systems, or laboratory databases is a plus.
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Strong written and verbal communication skills.
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Ability to work independently while knowing when to seek guidance or escalate an issue.
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Comfortable working in a fast-paced manufacturing environment with changing priorities.
Schedule & Training
This is a fully onsite B-Shift position following a 2-2-3 schedule :
6:00 PM–6:00 AM
The 2-2-3 schedule alternates workdays throughout a two-week cycle. For example, one week may be Sunday, Wednesday, and Thursday , followed by Monday, Tuesday, Friday, and Saturday the following week.
Training:
Training will initially be conducted Monday–Friday, 8:00 AM–5:00 PM before transitioning to the regular 6:00 PM–6:00 AM schedule.
Physical & Cleanroom Requirements
This role requires regular movement throughout laboratory, manufacturing, and classified cleanroom environments.
Candidates should be comfortable with:
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Standing and walking for extended periods.
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Stooping, bending, kneeling, crouching, reaching, and other routine physical activities associated with Environmental Monitoring.
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Handling laboratory equipment and materials.
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Lifting or carrying approximately 25–50 lbs. , with occasional pushing or pulling of heavier materials.
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Wearing required PPE and cleanroom garments for extended periods.
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Working in classified cleanroom environments while following required gowning and aseptic practices.
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Using computers, laboratory systems, and instrumentation for extended periods.
Why Consider This Opportunity?
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Up to $27/hour , based on experience.
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Long-term assignment currently scheduled through October 13, 2027 .
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Contract-to-hire opportunity.
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Potential for continued employment based on performance and business needs .
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Hands-on experience in sterile manufacturing and Environmental Monitoring .
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Opportunity to build experience within a highly regulated GMP pharmaceutical environment .
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Fully onsite role with a clearly defined 2-2-3 overnight schedule .
Pay Details: $25.00 to $27.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
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The California Fair Chance Act
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Los Angeles City Fair Chance Ordinance
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Los Angeles County Fair Chance Ordinance for Employers
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San Francisco Fair Chance Ordinance
Massachusetts Candidates Only: 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.
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