USA Quality Control Analyst I
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Job Location:
Hayward, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
16-10-2025
Vacancies:
1 Vacancy
Job Summary
Description:
Onsite position
Hayward CA 94545 / USA
Hours: 8am-4:30pm (flexible)
6 months contract ; May extend
Analyst I Quality Control Lab-Microbiology
Summary: Conduct environmental monitoring of ISO 5 7 8 and 9 cleanrooms at client manufacturing facilities along with Water collection. Support Microbiology analysis such as raw materials in-process and finished goods products samples at client manufacturing facility.
Conduct Microbiological analysis on raw materials initial in-process and final products and samples collected from the environmental monitoring programs at manufacturing facility.
Testing as required supporting Endotoxin testing Bioburden analysis growth promotion Will be required to read microbial plates and interpret test results.
QC Data entry in Sample manager- BaxLIMS
Complete all testing including special project / protocol testing in a timely and appropriate manner.
Perform equipment maintenance and calibrations as required.
Maintain data integrity and ensure compliance with company SOPs and specifications FDA GLP QSR and cGMP regulations.
Perform/or support all NCRs CAPAs and LIRs and be the point of contact for other departments for updates.
Participate in functions involving teams which impact production increase efficiency solve problems generate cost savings and improve quality.
Perform laboratory and manufacturing audits as required. Audit and update as required plant/lab SOPs.
Ensure Environmental Monitoring area is always maintained in a GMP state while following all EHS and 6S guidelines.
Flexibility in performing other duties as assigned or as business needs require.
Works and communicates effectively and professionally with others inside and outside the company.
Weekend work may be required as needed to meet production timeline schedules.
Qualifications
Ability to handle multiple tasks concurrently and complete tasks in a timely
manner.
Effective organizational skills and ability to plan and suggest resolutions to technical problems.
Demonstrates some knowledge of assays/equipment in functional area. Computers literate and competent with a general knowledge of word processing and spreadsheets (such as Microsoft Office).
Proficient use of laboratory equipment and tools. Must be detail oriented conscientious and responsible. Must have effective verbal and written communication skills. Some knowledge of applicable CTP/SOPsEHS requirements FDA Regulations application of CGMP/GDPs.
Must be able to learn about new computer systems and programs in a timely manner. Must be able to learn new computer systems and programs in a timely manner.
Education and/or Experience B.S. degree in Microbiology Biology; minimum 1-2-year experience in Pharmaceutical/Medical Device industry preferred.
Analyst I Quality Control Lab-Microbiology
Summary: Conduct environmental monitoring of ISO 5 7 8 and 9 cleanrooms at client manufacturing facilities along with Water collection. Support Microbiology analysis such as raw materials in-process and finished goods products samples at client manufacturing facility.
Conduct Microbiological analysis on raw materials initial in-process and final products and samples collected from the environmental monitoring programs at manufacturing facility.
Testing as required supporting Endotoxin testing Bioburden analysis growth promotion Will be required to read microbial plates and interpret test results.
QC Data entry in Sample manager- BaxLIMS
Complete all testing including special project / protocol testing in a timely and appropriate manner.
Perform equipment maintenance and calibrations as required.
Maintain data integrity and ensure compliance with company SOPs and specifications FDA GLP QSR and cGMP regulations.
Perform/or support all NCRs CAPAs and LIRs and be the point of contact for other departments for updates.
Participate in functions involving teams which impact production increase efficiency solve problems generate cost savings and improve quality.
Perform laboratory and manufacturing audits as required. Audit and update as required plant/lab SOPs.
Ensure Environmental Monitoring area is always maintained in a GMP state while following all EHS and 6S guidelines.
Flexibility in performing other duties as assigned or as business needs require.
Works and communicates effectively and professionally with others inside and outside the company.
Weekend work may be required as needed to meet production timeline schedules.
Qualifications
Ability to handle multiple tasks concurrently and complete tasks in a timely
manner.
Effective organizational skills and ability to plan and suggest resolutions to technical problems.
Demonstrates some knowledge of assays/equipment in functional area. Computers literate and competent with a general knowledge of word processing and spreadsheets (such as Microsoft Office).
Proficient use of laboratory equipment and tools. Must be detail oriented conscientious and responsible. Must have effective verbal and written communication skills. Some knowledge of applicable CTP/SOPsEHS requirements FDA Regulations application of CGMP/GDPs.
Must be able to learn about new computer systems and programs in a timely manner. Must be able to learn new computer systems and programs in a timely manner.
Education and/or Experience B.S. degree in Microbiology Biology; minimum 1-2-year experience in Pharmaceutical/Medical Device industry preferred.
Key Skills
- Computer
- IT Audit
- CAD CAM
- ABAP
- Exterior Designing
- HR Operations
