Quality Lab Technician

Actalent; Parker (CO); On-site; USD 40,000 - 42,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k)

Life Insurance

Short and long‑term disability

HSA

Transit benefits

PTO/Leave

Job summary

Actalent is seeking a Quality Technician in Parker, CO, to perform analyses and tests on materials and finished products. The role emphasizes accurate data, instrument calibration, and adherence to GMP/GDP in a regulated lab environment.

You will support non-conformances, document results, and collaborate with cross‑functional teams while following established procedures and safety protocols.

Qualifications

• Bachelor’s degree in biology, chemistry, microbiology, or related field OR associate degree with 3–5 years of relevant experience.
• 3+ years in a laboratory, quality, or analytical testing environment.
• Knowledge of quality control principles and analytical testing.

Responsibilities

• Perform analyses, inspections, and tests on raw materials, packaging materials, in-process samples, and finished products.
• Conduct qualitative and quantitative assays to support product release and process monitoring.
• Maintain and calibrate test instruments and lab equipment.

Skills

Quality control

Pipettes

Data analysis

Strong communication

Teamwork

Autonomy

Problem solving

Lab safety

Education

Bachelor’s degree in biology/chemistry/microbiology (or assoc. with 3–5 yrs experience)

Tools

Laboratory instruments

GMP/GDP

Job description

Job Title: Quality Technician

Job Description

The Quality Technician performs a wide range of laboratory analyses, inspections, and tests on raw materials, packaging materials, samples, and finished products to ensure they meet internal quality standards, customer expectations, and regulatory requirements. This role focuses on both qualitative and quantitative assays, supports the maintenance and certification of test instruments, and contributes to continuous improvement by investigating non-conformances and preparing quality reports. The position sits within a technician support career stream, providing technical support to production and operations while working with moderate autonomy and collaborating closely with internal teams.

Responsibilities

• Perform analyses, inspections, and tests on raw materials, packaging materials, in-process samples, and finished products to verify conformance to quality standards, customer requirements, regulatory expectations, and defined tolerance specifications for chemical and physical properties.

• Conduct a variety of qualitative tests and qualitative assays on samples to support product release, process monitoring, and validation activities.

• Perform quantitative assays on samples and finished products, ensuring accurate measurement, documentation, and interpretation of results.

• Aid in the maintenance, calibration, and certification of test instruments and laboratory apparatus to ensure they remain compliant and reliable for routine testing.

• Carry out required inspections, checks, analyses, and documentation of laboratory studies in accordance with established procedures and good documentation practices.

• Prepare, monitor, and analyze quality statistics and reports to identify trends, support decision‑making, and communicate quality performance.

• Review production records and documentation to confirm adherence to procedures, specifications, and quality system requirements.

• Conduct non‑conformance tests on manufactured, packaged, or tested products to determine the nature and extent of deviations from established standards.

• Apply problem‑solving tools and methodologies to investigate and determine root causes of non‑conformances, and propose corrective and preventive actions for supervisor review.

• Use schematics, diagrams, written procedures, and verbal instructions to perform testing and troubleshooting on electronic or mechanical components, equipment, or systems as needed.

• Gather, maintain, format, compile, and manipulate technical data using established formulas and procedures, and perform detailed mathematical calculations to support test results and reports.

• Run minor projects, including planning and performing tests, interpreting data, and developing clear, concise reports for internal stakeholders.

• Work under limited supervision as a seasoned individual contributor, exercising sound judgment on non‑routine technical tasks and escalating issues appropriately.

• Communicate with internal contacts to obtain and provide technical information on matters of moderate importance to the job area.

• Provide guidance, coaching, and training to other employees within the job area, supporting skill development and consistent application of quality procedures.

• Work comfortably with sheep and human blood samples, following all applicable safety and handling procedures.

• Use pipettes and other laboratory equipment accurately and consistently to perform assays and sample preparation.

• Support continuous improvement initiatives by suggesting and/or making improvements to optimize work processes within the laboratory and related operations.

Essential Skills

• Bachelor’s degree (BA/BS) in biology, chemistry, microbiology, or a related scientific field, or an associate degree combined with approximately 3–5 years of relevant technical experience.

• At least 3 years of relevant technical experience in a laboratory, quality, or analytical testing environment, including practical work and/or applicable training, education, or certification.

• Strong knowledge of quality control principles, including performing assays, analytical testing, qualitative tests, and testing of quantitative assays.

• Experience conducting non‑conformance tests and investigating root causes of non‑conformances using structured problem‑solving tools and methodologies.

• Hands‑on experience working with pipettes and standard laboratory equipment for sample preparation and testing.

• Working knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) in a regulated environment.

• Ability to use Microsoft Office applications to compile data, prepare reports, and communicate findings.

• Complete and broad knowledge of systems, techniques, tools, and procedures related to laboratory testing and quality assurance, typically obtained through prior work experience and training.

• Comfort and capability working with sheep and human blood samples in accordance with safety protocols.

• Strong verbal and written communication skills for documenting results, writing reports, and collaborating with internal teams.

• Ability to perform detailed mathematical calculations and conversions between English and metric measurement systems.

• Ability to work effectively as part of a team while also operating autonomously once trained.

Additional Skills & Qualifications

• Previous experience in the medical device industry, particularly in a regulated laboratory or manufacturing environment.

• Experience with CLIA and CAP regulatory frameworks and requirements for laboratory testing.

• Familiarity with Minitab or similar statistical analysis software for evaluating quality data and trends.

• Experience applying GMP and GDP in daily work, including accurate recordkeeping and adherence to written procedures.

• Proficiency with both English and metric measuring systems, including the ability to perform mathematical conversions between them.

• Demonstrated ability to suggest and implement improvements to optimize work processes and enhance laboratory efficiency.

• Experience providing guidance, coaching, or training to colleagues in a technical or laboratory setting.

• Strong collaboration skills and the ability to work well on cross‑functional teams.

• Comfort working in cold environments such as refrigerators when retrieving samples.

• Broad understanding of quality systems and regulatory expectations relevant to laboratory operations and product testing.

Work Environment

This role is based in a laboratory setting, where the Quality Technician works with a variety of biological samples, including sheep and human blood, as well as raw materials, packaging materials, and finished products. The work involves regular use of laboratory instruments, pipettes, and testing equipment, and may require occasional entry into refrigerated areas to retrieve samples. The schedule is Monday through Friday, 7:00 a.m. to 3:00 p.m. Once fully trained, the technician operates with a high degree of autonomy while still collaborating closely with internal teams. The role offers exposure to a leading national organization in its industry, with opportunities to extend the contract or pursue full‑time roles at this location or other locations globally. The environment emphasizes safety, regulatory compliance, and continuous learning, and supports professional growth through involvement in minor projects, data analysis, and cross‑functional communication.

Job Type & Location

This is a Contract position based out of Parker, CO.

Pay and Benefits

The pay range for this position is $28.85 - $30.29/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)

Workplace Type

This is a fully onsite position in Parker,CO.

Application Deadline

This position is anticipated to close on Sep 15, 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 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 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.

San 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.