Analytical Scientist

TekWissen • Eugene, OR

1d • Onsite

About The Position

The Analytical Scientist (also described as QC Scientist I / Quality Control Analyst) supports laboratory testing, quality assurance, and regulatory compliance in a pharmaceutical or biotechnology environment. The role performs analytical, chemical, biochemical, and microbiological testing; maintains accurate laboratory records; and supports equipment calibration, maintenance, troubleshooting, and laboratory investigations. Work must comply with applicable SOPs, cGMP, GLP, GDP, quality management system requirements, pharmacopeial standards, and regulatory guidelines. The position is a six-month temporary assignment, onsite in Eugene, Oregon.

Requirements

• Bachelor's degree in a scientific discipline; Chemistry, Biochemistry, Biology, Molecular Biology, or a related field is preferred.
• At least 2 years of experience in a quality control laboratory environment.
• Strong knowledge of cGMP, GLP, GDP, and quality management systems.
• Proficiency in analytical techniques such as HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, absorption spectroscopy, and dissolution testing.
• Knowledge of organic chemistry and analytical laboratory testing principles.
• Experience with microbiological testing methods and aseptic laboratory techniques.
• Ability to follow SOPs and maintain accurate laboratory documentation.
• Experience operating, maintaining, troubleshooting, and calibrating laboratory instrumentation.
• Proficiency with LIMS, Microsoft Office, and analytical data management software.
• Familiarity with applicable pharmacopeial standards and pharmaceutical regulatory requirements.
• Strong analytical, troubleshooting, and problem-solving abilities.
• Excellent attention to detail, organizational skills, and commitment to data accuracy.
• Effective written and verbal communication skills.
• Ability to work independently and collaboratively in a team-oriented laboratory environment.
• Strong time management skills and ability to handle multiple priorities.
• Flexibility to accommodate changing schedules and laboratory operational requirements.
• Ability to perform laboratory activities safely while wearing required PPE.

Nice To Haves

• Pharmaceutical or biotechnology industry experience.

Responsibilities

• Perform routine quality control laboratory testing and analytical analyses in accordance with established SOPs and regulatory requirements.
• Use applicable analytical techniques and instrumentation, including HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, absorption spectroscopy, and dissolution testing.
• Conduct chemical, biochemical, and microbiological testing to support product quality and compliance.
• Apply aseptic techniques and appropriate laboratory practices when performing microbiological testing.
• Prepare, analyze, and document laboratory samples using established procedures.
• Maintain accurate and detailed laboratory records in accordance with Good Documentation Practices.
• Operate, maintain, troubleshoot, and calibrate laboratory equipment.
• Record, review, and manage analytical data using LIMS, analytical software, and Microsoft Office applications.
• Follow cGMP, GLP, and applicable quality management system requirements.
• Support laboratory investigations, troubleshooting, and resolution of analytical or testing-related issues.
• Ensure laboratory activities comply with applicable pharmacopeial standards, regulatory guidelines, and internal quality procedures.
• Maintain a clean, organized, and safe laboratory environment and follow safety protocols and PPE requirements.
• Collaborate with laboratory personnel and cross-functional teams to support quality control operations.
• Manage multiple testing assignments and priorities while maintaining accuracy and meeting established timelines.

What This Job Offers