Analytical Scientist

TekWissen LLC

Eugene, OR
8 days ago

$30–$34

Highlights

As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to clients worldwide.

Numbers & Facts

Location	Eugene, OR
Industry	Computer/IT Services
Salary	$30–$34
Company Size	100 to 499 employees
Year Founded	2009
Website	http://www.tekwissen.com/

Description

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. The client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands.

Position: Analytical Scientist
Location: Eugene, OR 97402
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite

Shift: Wednesday to Sunday or Saturday to Wednesday - 11:00 PM to 07:30 AM

Summary

We are seeking a detail-oriented QC Scientist I / Quality Control Analyst to support laboratory testing, quality assurance, and regulatory compliance activities in a pharmaceutical or biotechnology environment. The ideal candidate will have hands-on experience with analytical testing techniques, laboratory instrumentation, microbiological testing, and quality control procedures. This position involves performing laboratory analyses, maintaining accurate documentation, supporting equipment calibration and maintenance, and ensuring compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and established Standard Operating Procedures (SOPs).

Responsibilities

Perform routine quality control laboratory testing and analytical analyses in accordance with established SOPs and regulatory requirements.
Utilize 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 requirements.
Apply aseptic techniques and appropriate laboratory practices when performing microbiological testing.
Prepare, analyze, and document laboratory samples using established testing procedures.
Maintain accurate and detailed laboratory records in accordance with Good Documentation Practices (GDP).
Operate, maintain, troubleshoot, and calibrate laboratory equipment to ensure reliable analytical performance.
Record, review, and manage analytical data using Laboratory Information Management Systems (LIMS), analytical software, and Microsoft Office applications.
Follow current Good Manufacturing Practices (cGMP), Good Laboratory Practices (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 while following established 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.

Required Skills

Bachelor's degree required, preferably in Chemistry, Biochemistry, Biology, Molecular Biology, or a related scientific discipline.
Minimum 2 years of experience in a quality control laboratory environment; pharmaceutical or biotechnology industry experience preferred.
Strong knowledge of current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Good Documentation Practices (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 Standard Operating Procedures (SOPs) and maintain accurate laboratory documentation.
Experience operating, maintaining, troubleshooting, and calibrating laboratory instrumentation.
Proficiency with Laboratory Information Management Systems (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 with the ability to handle multiple priorities effectively.
Flexibility to accommodate changing schedules and laboratory operational requirements.
Ability to perform laboratory activities safely while wearing required Personal Protective Equipment (PPE).

TekWissen Group is an equal opportunity employer supporting workforce diversity.

About Company

WE THE TEKWISSEN PEOPLE

TekWissen offers you a broader portfolio of services, industry-leading solutions, and the meaningful innovations that give you greater flexibility and speed to respond to market dynamics, reduced costs and risk to improve enterprise performance, and increased productivity to enable growth.

To keep pace with global market demands, TekWissen keeps its finger on the pulse of change. Our organized approach to guiding a project from its inception to closure. Managing projects is becoming more and more important as we enter the digital era. To cope with the pace that this transition demands, a method is required to manage projects so they can yield quality work, while incorporating efficient use of time and resources.

Project involves identifying which quality standards are relevant to the project and determining how to satisfy them.

It is important to perform quality planning during the Planning Process and should be done alongside the other project planning processes because changes in the quality will likely require changes in the other planning processes, or the desired product quality may require a detailed risk analysis of an identified problem. It is important to remember that quality should be planned, designed, then built in, not added on after the fact.

Capabilities and accomplishments in one TekWissen business enhance the opportunity for success in the others. Put simply, TekWissen's unique combination of attributes promotes success.