Quality Control Laboratory Technician

This entry-level Quality Control (QC) Laboratory Technician role supports a growing team in a GMP-regulated pharmaceutical environment. You will perform routine raw material testing and assist with analytical work in both Raw Materials QC and Chemistry laboratories. This position is ideal for someone early in their career who wants to build hands-on laboratory experience, gain exposure to pharmaceutical quality processes, and grow within a highly regulated setting.

Responsibilities

• Perform routine testing of raw materials, including Total Organic Carbon (TOC), conductivity, and basic analytical assays.
• Support the Chemistry laboratory by performing routine assay testing as needed.
• Help increase testing throughput and support a growing volume of raw material and chemistry samples.
• Work within a sample scheduling system to organize and manage daily and weekly testing workload.
• Execute testing in alignment with team priorities, timelines, and established laboratory procedures.
• Maintain accurate, complete, and compliant documentation in accordance with GMP standards.
• Collaborate closely with QC and Chemistry teams to ensure testing needs and timelines are met.
• Participate in monthly team meetings and engagement activities to support communication and continuous improvement.
• Follow laboratory safety practices and adhere to all relevant quality and compliance requirements.

• Bachelor’s degree in chemistry, biochemistry, biology, or a related scientific discipline.
• Previous academic chemistry laboratory experience with hands-on experimental work.
• Proficient pipetting skills and familiarity with wet chemistry techniques.
• Experience or coursework exposure to TOC (Total Organic Carbon) testing and basic analytical assays.
• Ability to work accurately within a GMP-regulated environment and follow written procedures.
• Strong attention to detail and commitment to maintaining precise laboratory records.
• Ability to manage workload using a sample scheduling system and meet established timelines.
• Effective communication skills and ability to work collaboratively within a laboratory team.

• Interest in building a long-term career in pharmaceutical quality control or analytical chemistry.
• Motivation to learn additional testing methods and support both QC and raw materials groups.
• Ability to adapt to varying sample volumes and a fast-paced laboratory environment.
• Willingness to participate in team meetings and engagement activities to support a positive team culture.

You will work in a QC testing laboratory within a large pharmaceutical manufacturing facility. The environment is fast-paced and lab-based, with variable sample volumes. Typical workload includes approximately 30–40 samples per week for TOC and conductivity testing, with peak periods reaching several hundred samples per week. Testing runs typically include 40–50 samples per run, and the workload is shared across a collaborative and diverse team. The schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m., for a 40-hour work week with a 30-minute unpaid lunch. The team culture is supportive, offers exposure to multiple types of testing across QC and raw materials groups, and provides strong opportunities to learn how the pharmaceutical industry operates and to grow professionally.

Job Type & Location

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

The pay range for this position is $25.00 - $28.00/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 Sanford,NC.

This position is anticipated to close on Jun 19, 2026.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 actalentaccommodation@actalentservices.com for other accommodation options.

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.