QC Scientist I
Job Location:
Eugene, OR - USA
Monthly Salary:
Posted on:
Vacancies:
Job Summary
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to clients worldwide. The job opportunity below is with one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment chemicals supplies and services essential in healthcare scientific research safety and education. As the global leader in serving the field of science the organization generates approximately $40 billion in annual revenue and is committed to helping customers make the world healthier cleaner and safer. Their global team delivers innovative technologies convenient procurement solutions and pharmaceutical services through industry-leading brands.
Position: QC Scientist I
Location: Eugene OR 97402
Duration: 5 Months
Job Type: Temporary Assignment
Work Type: Onsite
The QC Scientist I is responsible for performing laboratory testing and analytical evaluations to support the development and release of innovative therapeutic products. This role conducts quality control testing on raw materials in-process samples and finished products while ensuring compliance with cGMP GLP and quality management standards. The ideal candidate will have strong analytical skills laboratory experience and a commitment to maintaining high-quality documentation and regulatory compliance.
- Perform quality control testing of raw materials in-process samples and finished products.
- Conduct analytical testing using techniques such as HPLC ICP-MS UV-Vis spectroscopy dissolution testing and flow cytometry.
- Execute microbiological testing and aseptic techniques as required.
- Analyze interpret and document test results in accordance with Good Documentation Practices (GDP).
- Participate in investigations related to out-of-specification (OOS) results and laboratory deviations.
- Follow Standard Operating Procedures (SOPs) cGMP GLP and quality management system requirements.
- Maintain laboratory equipment through routine calibration maintenance and troubleshooting activities.
- Utilize LIMS analytical software and Microsoft Office applications to record and manage data.
- Support continuous improvement initiatives and quality enhancement programs.
- Collaborate with cross-functional teams while effectively managing multiple priorities.
- Bachelors degree in Chemistry Biochemistry Biology Molecular Biology or a related scientific field.
- Minimum of 3 years of experience in a Quality Control laboratory environment preferably within the pharmaceutical or biotechnology industry.
- Strong knowledge of cGMP GLP and quality management systems.
- Experience with analytical techniques including:
- HPLC
- ICP-MS
- UV-Vis Spectroscopy
- Dissolution Testing
- Flow Cytometry
- Experience with microbiological testing methods and aseptic laboratory practices.
- Strong documentation skills and adherence to GDP requirements.
- Proficiency with LIMS Microsoft Office Suite and analytical software platforms.
- Excellent analytical organizational and problem-solving skills.
- Strong written and verbal communication abilities.
- Ability to work independently and collaboratively in a team environment.
- Experience in pharmaceutical biotechnology or life sciences manufacturing environments.
- Knowledge of pharmacopeia standards and regulatory requirements.
- Experience supporting laboratory investigations and continuous improvement initiatives.
TekWissen Group is an equal opportunity employer supporting workforce diversity.
