3rd Shift QC Chemist

Actalent; High Point (NC); On-site; USD 32,000 - 34,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Life Insurance

Short and long-term disability

HSA

Transit benefits

Employee Assistance Program

PTO / Vacation

Job summary

Actalent is seeking a Quality Control Laboratory Technician for a 2-2-3 night shift in High Point, NC, with initial day-shift training for 3–4 weeks. You will perform routine chemical analyses, operate GC/HPLC, and ensure GMP/GLP compliance in an ISO-certified facility.

The role emphasizes data integrity, precise documentation, and collaboration with production and quality teams. A strong chemistry background and lab experience are required, with growth into R&D possible over time.

Qualifications

• Bachelor's degree in Chemistry; other scientific degrees may be considered when combined with prior chemical manufacturing experience.
• 13 years of experience working in a laboratory setting, preferably within industry.
• 13 years of hands-on experience with GC and HPLC.
• Demonstrated proficiency with standard chemical laboratory equipment and instrumentation.
• Experience performing chemical analysis and wet chemistry techniques in a quality control environment.
• Ability to follow GMP/GLP documentation practices in daily work.
• Knowledge of SOPs and the ability to adhere to them consistently.
• Familiarity with ISO-certified facilities.
• Strong troubleshooting abilities related to laboratory tests and instrumentation.
• Attention to detail and accuracy in recording and reporting test results.

Responsibilities

• Perform daily quality control testing and chemical analyses on production samples using standard laboratory equipment and specialized instrumentation.
• Operate and maintain GC and HPLC platforms and other analytical instruments.
• Conduct wet chemistry procedures, pH measurements, viscosity checks, and routine assays to ensure product specifications.
• Record test results on batch sheets and enter data into LIMS as required.
• Follow GMP/GLP SOPs for testing and documentation.
• Work in ISO-certified facilities ensuring compliance with quality requirements.
• Troubleshoot instrument/test issues and escalate complex problems to technical staff.
• Communicate findings to production and quality teams for timely decisions.
• Collaborate with night-shift staff to resolve technical or procedural issues.
• Maintain a safe, organized lab space when handling chemical products.

Skills

Laboratory testing

Instrument troubleshooting

GLP/GMP compliance

Data entry in LIMS

Attention to detail

Inter-team communication

Education

Bachelor's degree in Chemistry

13 years laboratory experience

Tools

Gas Chromatography (GC)

High Performance Liquid Chromatography (HPLC)

Thermogravimetric Analysis (TGA)

Differential Scanning Calorimetry (DSC)

Capillary rheometry

Melt indexers

Viscosity measurements

LIMS

Job description

Job Title: Quality Control Laboratory Technician Shift: 2-2-3 schedule ( 5PM to 5AM ) and will train on 8 hour day shift for 3-4 weeks prior to moving to 12-hour shift. Job Description This role is a hands-on, chemistry-focused Quality Control Laboratory Technician position within a large chemical processing facility. You will perform routine and specialized chemical analyses to support production quality, using a variety of laboratory instruments and following established procedures and documentation standards. The position offers the opportunity to grow within the Quality Department and potentially transition into research and development roles over time. Responsibilities

• Perform daily quality control testing and chemical analyses on production samples using standard laboratory equipment and specialized instrumentation.
• Operate and maintain advanced analytical instruments such as thermogravimetric analysis and differential scanning calorimetry platforms, capillary rheometers, melt indexers, gas chromatographs (GC), and high performance liquid chromatographs (HPLC).
• Conduct wet chemistry procedures, pH measurements, viscosity checks, and other routine assays to ensure products meet established specifications.
• Accurately record test results on batch sheets and enter data into the Laboratory Information Management System (LIMS) when required.
• Follow Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Standard Operating Procedures (SOPs) for all testing and documentation activities.
• Work in accordance with quality standards in an ISO-certified facility, ensuring compliance with internal and external quality requirements.
• Troubleshoot basic instrument and testing issues, and elevate complex problems to technical staff as needed.
• Communicate test findings clearly and promptly to production and quality teams to support timely decision-making.
• Collaborate with technical staff on the night shift, asking questions and seeking guidance to resolve technical or procedural issues.
• Maintain a safe and organized laboratory workspace while working with chemical products and processing materials.

Essential Skills

• Bachelors degree in Chemistry; other scientific degrees may be considered when combined with prior chemical manufacturing experience.
• 13 years of experience working in a laboratory setting, preferably within industry.
• 13 years of hands-on experience with Gas Chromatography (GC) and High Performance Liquid Chromatography (HPLC).
• Demonstrated proficiency with standard chemical laboratory equipment and instrumentation.
• Experience performing chemical analysis and wet chemistry techniques in a quality control environment.
• Ability to follow and apply GMP/GLP documentation practices in daily work.
• Knowledge of Standard Operating Procedures (SOPs) and the ability to adhere to them consistently.
• Familiarity with working in an ISO-certified facility.
• Strong troubleshooting abilities related to laboratory tests and instrumentation.
• Attention to detail and accuracy in recording and reporting test results.

Additional Skills & Qualifications

• Experience using a Laboratory Information Management System (LIMS) is a plus.
• Experience in chromatography, including GC and HPLC, and related analytical methods.
• Experience with thermogravimetric analysis and differential scanning calorimetry is beneficial.
• Exposure to capillary rheometry, melt indexers, and viscosity measurements is advantageous.
• Previous industry laboratory experience is preferred over purely academic or non-laboratory backgrounds.
• Ability to work effectively on a night shift schedule and adapt to a rotating 2-2-3 shift pattern.
• Strong communication skills for interacting with technical staff and production personnel.
• Interest in long-term career growth within quality control and potential progression into research and development roles.

Work Environment

This position is based in a large specialty chemicals manufacturing facility on a substantial industrial site. You will work primarily in a laboratory setting that is closely integrated with production areas and deals directly with chemical products. The environment is more industrial than pharmaceutical, and the lab and production spaces are not highly cleanroom-style; candidates should be comfortable working in a setting where surfaces and equipment may be exposed to process materials. The facility operates under ISO certification and emphasizes structured procedures, documentation, and quality-focused culture, offering stability and opportunities for advancement for high-performing laboratory technicians.

Job Type & Location

This is a Contract to Hire position based out of High Point, NC.

Pay and Benefits

The pay range for this position is $23.00 - $25.00/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 to Hire position based out of High Point, NC.

Application Deadline

This position is anticipated to close on Oct 22, 2026.

Workplace Type

This is a fully onsite position in High Point,NC.

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.

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 [e-mail] for other accommodation options.