QC Scientist I

Actalent; Eugene (OR); On-site; USD 36,000 - 41,000; Full time

Benefits offered by this job

Paid time off

Medical, dental, vision

401(k) retirement plan

Life insurance

Short/long-term disability

Health Savings Account

Transportation benefits

Job summary

Actalent is seeking a QC Scientist I to join our regulated laboratory team in Eugene, OR. You will perform routine quality control testing, maintain equipment, and document results in compliance with cGMP, GLP, GDP and SOPs. The role requires hands-on analytical skills and meticulous data integrity.

You will work with instruments such as HPLC, ICP-MS, UV-Vis, and NMR, and use LIMS to manage data. This is a contract position offering comprehensive benefits and a stable, detail‑oriented work

Qualifications

• Minimum 2 years in a quality control lab.
• Familiar with cGMP/GLP/GDP and QA systems.
• Experience with analytical instrumentation.
• Ability to document results per SOPs.
• Experience calibrating and maintaining equipment.
• Bachelor’s degree in a scientific field.
• Experience with GDP documentation practices.

Responsibilities

• Perform QC testing using established methods and instrumentation.
• Prepare samples, reagents, standards, and solutions.
• Conduct testing with HPLC, ICP-MS, UV-Vis, flow cytometry, NMR, dissolution testing and related techniques.
• Analyze data and interpret results for accuracy and reliability.
• Escalate unexpected results and investigate as appropriate.
• Maintain complete, accurate, and traceable records per quality systems.
• Operate, calibrate, and troubleshoot laboratory instrumentation.
• Use LIMS and software to enter, track, and report data.
• Follow PPE, safety and contamination-control procedures.

Skills

cGMP/GLP/GDP

Analytical instrumentation

SOP adherence

Data documentation

Quality systems

Microsoft Office

Education

Bachelor's degree in science

Tools

HPLC

ICP-MS

UV-Vis

Flow cytometry

NMR

Dissolution testing

LIMS

Job description

Job Title: QC Scientist I

Job Description

The QC Scientist I performs analytical and quality control testing in a regulated laboratory environment. In this role, you execute established analytical methods, analyze and document results, maintain laboratory equipment, and ensure all laboratory activities comply with cGMP, GLP, GDP, and applicable quality requirements. You work independently with a strong scientific foundation in analytical chemistry, biochemistry, biology, or a related discipline, demonstrating exceptional attention to detail and the ability to troubleshoot analytical and laboratory issues within established quality systems.

Responsibilities

• Perform routine and non-routine quality control testing using established analytical methods and instrumentation.
• Prepare samples, reagents, standards, and solutions according to defined procedures.
• Conduct testing using techniques such as HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, absorption-based methods, dissolution testing, and general organic chemistry techniques.
• Analyze and interpret laboratory results, ensuring accuracy and reliability of data.
• Identify unexpected results or testing issues and promptly elevate or investigate as appropriate.
• Execute all laboratory activities in accordance with cGMP, GLP, GDP, SOPs, and established quality management systems.
• Maintain complete, accurate, and traceable laboratory records that meet data integrity and documentation review requirements.
• Follow applicable pharmacopeia standards and regulatory requirements during testing and documentation.
• Support laboratory investigations, deviations, and corrective actions when required.
• Support microbiological testing activities as needed, following proper procedures and protocols.
• Utilize proper aseptic technique when handling samples and materials to prevent contamination.
• Follow contamination-control practices and laboratory safety procedures at all times.
• Operate, maintain, and calibrate laboratory instrumentation to ensure optimal performance.
• Perform routine troubleshooting on laboratory instruments to resolve performance issues.
• Document equipment maintenance and calibration activities in accordance with quality and regulatory expectations.
• Use LIMS and analytical software to enter, track, review, and report laboratory data.
• Maintain an organized laboratory environment and comply with PPE and safety requirements.

Essential Skills

• Minimum 2 years of experience in a quality control laboratory environment.
• Strong understanding of cGMP, GLP, GDP, and quality management systems.
• Hands‑on experience with analytical laboratory instrumentation and testing techniques.
• Ability to execute testing according to established SOPs and accurately document results.
• Experience maintaining, calibrating, and troubleshooting laboratory equipment.
• Bachelors degree in a scientific discipline, preferably chemistry, biochemistry, biology, molecular biology, or a related field.
• Experience following SOPs and GDP documentation practices.
• Hands‑on analytical laboratory experience in a regulated environment.
• Strong computer skills, including proficiency with Microsoft Office and laboratory software.
• Strong analytical and problem‑solving abilities.

Additional Skills & Qualifications

• Biotechnology or pharmaceutical quality control experience.
• Experience with HPLC, ICP‑MS, UV‑Vis spectroscopy, flow cytometry, NMR, and dissolution testing.
• Microbiological testing experience and familiarity with aseptic technique.
• Experience using LIMS to manage and review laboratory data.
• Knowledge of pharmacopeia standards and applicable regulatory requirements.

Work Environment

This role is based in a regulated laboratory environment that emphasizes compliance with cGMP, GLP, GDP, and established quality systems. You work with a variety of analytical instruments and technologies, including HPLC, ICP‑MS, UV‑Vis spectroscopy, flow cytometry, NMR, dissolution testing equipment, and general organic chemistry tools, as well as LIMS and other analytical software. The laboratory follows strict contamination‑control and safety procedures, and appropriate PPE is required. The position offers a comprehensive benefits package, including paid time off, paid holidays, medical, dental, and vision coverage, a 401(k) retirement plan, a health savings account, life insurance, short‑term and long‑term disability, an employee assistance program, and transportation benefits, supporting a stable and well‑rounded work experience.

Job Type & Location

This is a Contract position based out of Eugene, OR.

Pay And Benefits

The pay range for this position is $26.00 - $30.00/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)

Application Deadline

This position is anticipated to close on Nov 11, 2026.

Workplace Type

This is a fully onsite position in Eugene,OR.

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.

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.