QC Analyst II
QC Analyst II
Posted on :
26-09-2025
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1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
26-09-2025
Job Description
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing scientific expertise and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients Bioscience Biopharmaceuticals Custom manufacturing Biotechnology Life science ingredients Nutrition Microbial Control Agriculture Materials Science Personal Care and cell and gene therapy.
Job Title: QC Analyst II
Location: Vacaville CA 95688
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Job Description:
Summary
- With limited supervision QC Associate II is responsible for the performance of direct materials testing in accordance with cGMP regulations.
- These duties include execution of laboratory testing trend analysis documentation review support of discrepancies (OOS OOT OOE) and other laboratory support activities.
- In conjunction with Quality Control leadership the QC Associate II works to meet departmental and organizational goals.
Responsibilities
- Perform a broad variety of basic and moderately complex tests with documentation according to GMP
- Review data and assess against established acceptance criteria
- Perform technical review of peer-generated data
- Evaluate data to identify trends and/or establish limits
- Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed
- Identify and troubleshoot technical problems
- Identify gaps in systems and procedures
- Receive and provide training
- Participate in assay transfer and assay validation
- Perform equipment qualification / maintenance
- Prepare and maintain standards controls stocks cultures etc. per established procedures
- Support the maintenance and compliance of operational areas
- Assure and apply GMP throughout operations
- Coordinate with customers to support multi-site operational activities
- Support internal and external audits and regulatory inspections
- Works to meet schedules timelines deadlines
- Participate in and/or lead group and project teamwork; project and process improvements
- Write protocols and reports under limited supervision
- Meets scheduled performance of 95% on time
- Perform other duties as requested by managers to support Quality activities
Requirements
- B.S. /B.A. degree and three years experience or Masters Degree plus one year experience or an equivalent combination of education and experience.
- Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry.
- Strong verbal and written communication skills ability to organize and present information both formally and informally.
- Demonstrated ability to apply knowledge of scientific theories principles and techniques used in analytical or biological test procedures.
- Routinely exercises sound judgment reasoning and problem solving.
- Capable of working under limited supervision and determining own short term priorities.
TekWissen Group is an equal opportunity employer supporting workforce diversity.
Employment Type
Full-time
Key Skills
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