Job 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: Quality Control Scientist I
Location: Cincinnati OH 45237
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Location: Cincinnati OH 45237
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Monday To Friday - First Shift - Should start the shift between 06:00 AM to 09:00 AM
Summary
We are seeking a detail-oriented Quality Control Scientist I. The ideal candidate will have hands-on experience with High-Performance Liquid Chromatography (HPLC), chemical testing, and analytical laboratory techniques. This position involves testing pharmaceutical finished products and stability samples, performing routine analytical procedures, and ensuring compliance with established quality and regulatory standards.
Responsibilities
- Perform routine chemical testing of pharmaceutical finished products and stability samples using established analytical methods.
- Conduct analytical testing for product strength, impurities, identity, and other quality characteristics using HPLC, dissolution, and wet chemistry techniques.
- Operate analytical laboratory instrumentation and perform routine calibrations and verifications.
- Prepare mobile phases, diluents, reagents, and other laboratory solutions.
- Identify, document, and report out-of-specification (OOS) results and unexpected analytical findings.
- Maintain accurate laboratory records, test results, and supporting documentation.
- Follow established Standard Operating Procedures (SOPs), Good Manufacturing Practices (cGMP), and Good Laboratory Practices (GLP).
- Maintain laboratory equipment and work areas in accordance with safety and quality standards.
- Support QC laboratory activities, testing schedules, and manufacturing operations.
- Troubleshoot routine analytical issues and communicate findings effectively.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related physical science discipline.
- 1 2 years of experience in chemical or analytical laboratory testing using HPLC or GC techniques.
- Equivalent combinations of education, training, and relevant laboratory experience may be considered.
- Hands-on experience and working knowledge of HPLC instrumentation are required.
- Knowledge of analytical chemistry, qualitative and quantitative testing, laboratory instrumentation, wet chemistry techniques, and sample preparation.
- Understanding of cGMP, GLP, SOPs, and pharmaceutical quality and regulatory standards.
- Ability to accurately document analytical results, follow established laboratory procedures, and maintain compliance with safety and quality guidelines.
- Strong analytical, troubleshooting, problem-solving, and organizational skills with excellent attention to detail.
- Effective written and verbal communication skills, with the ability to multitask and work efficiently in a fast-paced laboratory environment.
- Ability to stand, walk, bend, and perform laboratory activities for extended periods.
- Ability to lift and move materials weighing approximately 10 35 lbs.
- Ability to operate laboratory equipment safely and wear required personal protective equipment (PPE).
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Numbers & Facts
| Location | Cincinnati, OH |
| Industry | Computer/IT Services |
| Salary | $20–$25 |
| Company Size | 100 to 499 employees |
| Year Founded | 2009 |
| Website | http://www.tekwissen.com/ |
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.Skills
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