Highlights
The Analytical Chemist/ Quality Control professional is responsible for performing analytical and functional testing of raw materials, intermediates, and finished goods kits in accordance with approved SOPs and cGMP requirements. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer.
Numbers & Facts
| Location | Fremont, CA |
| Industry | Computer/IT Services |
| Salary | $30–$32 |
| 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 our clients worldwide. The job opportunity below is for 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, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.
Position: Analytical Chemist
Location: Fremont, CA 94538
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Summary
The Analytical Chemist/ Quality Control professional is responsible for performing analytical and functional testing of raw materials, intermediates, and finished goods kits in accordance with approved SOPs and cGMP requirements. This role involves laboratory testing, accurate documentation, data analysis, and supporting investigations to ensure products meet established quality standards.
Responsibilities
- Conduct analytical and functional testing of raw materials, intermediates, and finished goods kits according to approved SOPs.
- Perform testing using chemistry clinical analyzers and accurately document test results using SOPs and electronic workbooks.
- Complete batch records and maintain accurate laboratory documentation in accordance with cGMP requirements.
- Support laboratory investigations by gathering and evaluating relevant information and following established processes.
- Summarize and evaluate test data and maintain accurate lot histories.
- Review data for trends, excursions, and potential quality issues according to established procedures.
- Perform basic data analysis, including calculations of concentrations and dilutions.
- Follow laboratory safety procedures when handling biohazardous materials, hazardous chemicals, and controlled substances.
- Maintain a clean, organized, and compliant laboratory environment.
- Communicate test results, findings, and quality concerns clearly to team members and management.
- Perform additional responsibilities as assigned by the Supervisor.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, Bioscience, or a related field required; equivalent experience may be considered.
- 0 2 years of Quality Assurance or Quality Control experience, preferably within the medical diagnostics industry.
- Strong laboratory skills, including pipetting and safe handling of biohazardous and hazardous chemical materials.
- Understanding of cGMP requirements and their application in a laboratory environment.
- Ability to accurately follow written and verbal instructions.
- Strong reading comprehension and documentation skills.
- Excellent verbal and written communication skills.
- Intermediate proficiency with word processing and spreadsheet software.
- Ability to manage multiple tasks simultaneously and work independently.
- Basic data analysis and mathematical skills, including concentration and dilution calculations.
- Strong understanding of algebraic concepts.
- High attention to detail and accuracy.Ability to work in a controlled laboratory environment.
- Exposure to controlled substances may be required as part of job responsibilities.
- Must strictly follow applicable safety protocols and procedures when handling controlled substances.
- Successful completion of required background screening, including screening related to controlled substances.
- Ability to follow cGMP, laboratory safety, and company compliance requirements.
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.