QC Scientist I

Job Title: QC Scientist I Job Description
The QC Scientist I serves as a Quality Control Laboratory Analyst responsible for performing routine analytical and microbiological testing in support of quality control operations. This role operates within a regulated laboratory environment, ensuring accurate testing, thorough documentation, and full compliance with applicable quality standards and regulatory requirements. The position is ideal for a highly detail-oriented scientist with strong technical laboratory skills who thrives in a quality-focused, data-driven setting.
Responsibilities
- Perform routine analytical testing using HPLC, ICP-MS, UV-Vis spectroscopy, dissolution testing, and other laboratory techniques to support quality control operations.
- Conduct microbiological testing and support aseptic laboratory operations in accordance with established procedures.
- Follow all applicable SOPs and adhere to cGMP, GLP, and GDP requirements to ensure regulatory compliance and robust quality standards.
- Accurately document testing results, maintain complete laboratory records, and uphold data integrity standards at all times.
- Perform routine equipment maintenance, calibration, and basic troubleshooting for analytical instruments and laboratory equipment.
- Utilize LIMS and other laboratory software systems to manage, track, and report testing data efficiently and accurately.
- Investigate and report deviations, out-of-specification (OOS) results, and atypical findings in accordance with quality procedures.
- Support continuous improvement initiatives and quality enhancement projects within the laboratory and broader quality organization.
- Collaborate closely with laboratory and quality teams to support production schedules, testing priorities, and product release timelines.
- Maintain a clean, organized, and compliant laboratory workspace that supports safe and efficient operations.
Essential Skills
- Experience working in a regulated quality control laboratory environment following cGMP and GLP requirements.
- Proficiency with analytical instrumentation, particularly HPLC, and familiarity with common laboratory testing techniques.
- Strong understanding of SOP adherence, GDP documentation practices, and quality management systems.
- Ability to investigate test results, maintain data integrity, and support overall quality operations.
- Experience with LIMS and other laboratory software systems for data entry, tracking, and reporting.
- Knowledge of aseptic technique and microbiological testing principles.
- Bachelors degree in Chemistry, Biochemistry, Biology, Molecular Biology, or a related scientific field.
- Strong computer proficiency, including Microsoft Office applications and laboratory informatics tools.
- Excellent organizational skills with the ability to manage documentation and multiple tasks effectively.
- Clear and professional communication skills, both written and verbal.
- High level of attention to detail and accuracy in all aspects of laboratory work.
- Strong analytical and troubleshooting skills for interpreting data and resolving technical issues.
Additional Skills & Qualifications
- Biotech or pharmaceutical industry experience.
- Hands-on experience with microbiological testing in a QC or regulated laboratory environment.
- Experience using LIMS for sample management and data reporting.
- Practical experience with ICP-MS, dissolution testing, and UV-Vis spectroscopy.
- Knowledge of pharmacopeia requirements and relevant regulatory standards.
- Ability to manage multiple priorities and adapt to changing project needs.
- Self-motivated and accountable, with a strong sense of ownership for assigned tasks.
- Effective interpersonal skills and the ability to collaborate as a supportive team player.
- Adaptable and flexible mindset suited to a dynamic, quality-focused environment.
Work Environment
This role is based in a regulated quality control laboratory environment that emphasizes accuracy, compliance, and collaboration. You will work daily with advanced analytical instruments such as HPLC, ICP-MS, UV-Vis spectrophotometers, dissolution testers, and microbiological testing equipment, as well as LIMS and other laboratory software systems. The work involves following cGMP, GLP, GDP, and established SOPs, with a strong focus on data integrity and quality management. The environment supports cross-functional collaboration with laboratory and quality teams to meet production and product release timelines. Team members benefit from a comprehensive benefits package that typically includes paid time off, paid holidays, medical, dental, and vision coverage, a 401(k) retirement plan, health savings account options, life insurance, short-term and long-term disability coverage, an employee assistance program, and transportation-related benefits. The culture values attention to detail, continuous improvement, accountability, and effective communication in a professional scientific setting.
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)
Workplace Type
This is a fully onsite position in Eugene,OR.
Application Deadline
This position is anticipated to close on Oct 21, 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 [email protected] 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
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