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Job Requirements of Quality Control Analyst I:
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Employment Type:
Contractor
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Location:
Hayward, CA (Onsite)
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Quality Control Analyst I
Careers Integrated Resources Inc
Hayward, CA (Onsite)
Contractor
Job Title:Analyst I, Quality Control Lab-Microbiology
Location: Alexander CT 21020 or Hayward, CA 94545 (Onsite position)
Hours: 8am-4:30pm (flexible)
Duration: 7 Months+ contract
Pay: $25/hr. on W2
Summary:
Qualifications
Location: Alexander CT 21020 or Hayward, CA 94545 (Onsite position)
Hours: 8am-4:30pm (flexible)
Duration: 7 Months+ contract
Pay: $25/hr. on W2
Summary:
- Conduct environmental monitoring of ISO 5, 7, 8, and 9 cleanrooms at *** manufacturing facilities along with Water collection. Support Microbiology analysis such as raw materials, in-process and finished goods products samples at *** 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.
- 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/SOPs, EHS 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.
- B.S. degree in Microbiology, Biology; minimum 1-2-year experience in Pharmaceutical/Medical Device industry preferred.
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