Analytical Scientist

TekWissen•Eugene, OR

6h•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 laboratory analyses and maintains accurate records while supporting equipment calibration and maintenance and complying with cGMP, GLP, GDP, SOPs, and applicable quality requirements. This is a six-month temporary, onsite assignment in Eugene, Oregon. The schedule is either Wednesday through Sunday or Saturday through Wednesday, from 11:00 PM to 7:30 AM. The position requires hands-on analytical and microbiological testing experience, the safe use of laboratory equipment and PPE, and the ability to manage multiple testing priorities accurately and on time.

Requirements

Bachelor's degree, preferably in Chemistry, Biochemistry, Biology, Molecular Biology, or a related scientific discipline.
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.
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 effectively.
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 SOPs and regulatory requirements.
Use analytical techniques and instrumentation such as HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, absorption spectroscopy, and dissolution testing, as applicable.
Conduct chemical, biochemical, and microbiological testing to support product quality and compliance.
Apply aseptic techniques and appropriate laboratory practices during microbiological testing.
Prepare, analyze, and document laboratory samples using established procedures.
Maintain accurate 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, troubleshoot issues, and help resolve analytical or testing-related problems.
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 timelines.