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Analytical Chemist

TekWissen LLC
  • Cincinnati, OH
  • $20–$25
  • Quick Apply
1 day ago

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: Analytical Chemist
Location: Cincinnati OH 45237
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Summary:
The Analytical Chemist / QC Scientist I performs routine analytical testing and documentation to support pharmaceutical manufacturing operations within a QC Analytical Chemistry Laboratory. The role focuses on residual active pharmaceutical ingredient and detergent analysis using chromatographic and instrumental techniques such as HPLC, Mass Spectrometry, and TOC. The position requires a Bachelor's degree or higher in a physical science, preferably Chemistry. Experience with chemical testing using chromatographic techniques is preferred.
Responsibilities
  • Perform routine chemical testing of residual swab samples using internally developed and validated test methods.
  • Perform pharmaceutical residual analysis using HPLC, Mass Spectrometry, and TOC techniques.
  • Recognize, investigate, and report out-of-specification (OOS), unexpected, and non-routine analytical or product results.
  • Perform daily instrument calibrations and verifications as required.
  • Accurately document testing activities, analyses, observations, and results.
  • Record and report analytical results according to laboratory procedures and systems.
  • Prepare test solutions, including diluents and mobile phases.
  • Clean and maintain laboratory work areas and instrumentation.
  • Perform testing in compliance with SOPs, GMP, GLP, and safety requirements.
  • Maintain required company and facility compliance status.
  • Support internal development and pharmaceutical manufacturing operations.
  • Review and communicate analytical test results accurately and effectively.
  • Manage testing workload and schedule activities to meet required timelines.
  • Seek additional assignments when primary testing responsibilities are completed.
  • Participate in training and learning opportunities to develop technical skills.
  • Share knowledge and skills with other laboratory team members.
  • Follow company policies, SOPs, cGMPs, work instructions, analytical methods, and analyst guidelines.
Required Skills
  • Bachelor's degree or higher in Physical Science, preferably Chemistry.
  • 1 2 years of experience performing chemical testing using chromatographic techniques is preferred.
  • Working theoretical and practical knowledge of HPLC and Mass Spectrometry.
  • Knowledge of basic instrumental technologies.
  • Understanding of qualitative and quantitative chemical analysis.
  • Awareness of pharmaceutical industry quality and regulatory requirements.
  • Strong scientific problem-solving and logical reasoning skills.
  • Ability to identify and appropriately communicate OOS and unexpected results.
  • Ability to read and interpret technical procedures and governmental regulations.
  • Ability to perform mathematical calculations related to test reliability, analysis of variance, and correlation techniques.
  • Strong written and verbal communication skills.
  • Ability to multitask and manage time effectively in a fast-paced laboratory environment.
  • Ability to work independently and take initiative in pursuing training and learning opportunities.
  • Ability to collaborate effectively and share technical knowledge with team members.
  • Ability to follow GMP, GLP, SOP, safety, and laboratory requirements.
  • Ability to work with laboratory instruments, computers, and analytical equipment for prolonged periods.
  • Ability to stand, walk, stoop, kneel, and crouch periodically or for extended periods.
  • Ability to lift, carry, and move light to medium weights of approximately 10 35 lbs.
  • Manual dexterity for handling equipment, grasping, typing, and laboratory activities.
  • Ability to read materials, operate equipment, and use computer monitors for prolonged periods.
  • Ability to wear required PPE, including safety glasses, safety shoes, lab coat, gloves, safety apron, and an organic respirator when required.
TekWissen Group is an equal opportunity employer supporting workforce diversity.

Numbers & Facts

LocationCincinnati, OH
IndustryComputer/IT Services
Salary$20–$25
Company Size100 to 499 employees
Year Founded2009
Websitehttp://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

  • Active Pharmaceutical Ingredient (API)unmatched
  • Analysis Skillsunmatched
  • Analytical Chemistryunmatched
  • Biotech and Pharmaceuticalunmatched
  • Chemistryunmatched
  • Chromatographic Assayunmatched
  • Chromatographyunmatched
  • Cleanroomunmatched
  • Communication Skillsunmatched
  • Corporate Complianceunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Diversityunmatched
  • Drug Developmentunmatched
  • Drug Manufacturingunmatched
  • GLP (Good Laboratory Practices)unmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Government Regulationsunmatched
  • Healthcareunmatched
  • High Performance Liquid Chromatography (HPLC)unmatched
  • Instrumentationunmatched
  • Investigative Reportsunmatched
  • Laboratoryunmatched
  • Laboratory Analysisunmatched
  • Laboratory Equipmentunmatched
  • Laboratory Techniquesunmatched
  • Manual Dexterityunmatched
  • Manufacturing Operationsunmatched
  • Mass Spectrometryunmatched
  • Mathematicsunmatched
  • Multitaskingunmatched
  • Operational Supportunmatched
  • Pharmaceutical Analysisunmatched
  • Physical Scienceunmatched
  • Presentation/Verbal Skillsunmatched
  • Problem Solving Skillsunmatched
  • Product Developmentunmatched
  • Purchasing/Procurementunmatched
  • Quality Assurance Methodologyunmatched
  • Quality Controlunmatched
  • Quantitative Analysisunmatched
  • Regulatory Requirementsunmatched
  • Reliability Analysisunmatched
  • Reliability Testingunmatched
  • Safety Trainingunmatched
  • Scientific Researchunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Support Documentationunmatched
  • Team Playerunmatched
  • Technical Deliveryunmatched
  • Test Plan/Scheduleunmatched
  • Testingunmatched
  • Time Managementunmatched
  • Typingunmatched
  • Variance Analysisunmatched
  • Workforce Managementunmatched
  • Writing Skillsunmatched

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