QC Analyst I: Life Sciences Lab & LIMS

Bio-Rad Laboratories; Irvine (CA); On-site; USD 70,000 - 85,000; Full time

Benefits offered by this job

Competitive medical plans

HSA funds

Fertility stipend

401k + profit sharing

Employee stock purchase program

Mental health platform

Learning & development opportunities

Paid time off

Employee Resource Groups

Job summary

Bio-Rad Laboratories in Irvine, CA is seeking a Quality Control Specialist I to inspect and test biological raw materials and intermediates, perform sampling, review results, and log data into ERP and LIMS per established procedures.

You will identify out-of-spec or out-of-trend results, assist with testing improvements within change management, and work closely with a team while following GMP/GDP and good laboratory practices to ensure product quality.

Qualifications

• Bachelor’s degree, or equivalent, in a life science or related field.
• 0-2 years in a laboratory environment or equivalent.
• Experience with clinical laboratory techniques and instruments are a plus.
• Ability to work independently or as part of a team to complete projects within required timeframes.
• Good time management, organizational and analytical skills.
• Experience with Good Manufacturing and Documentation Practices (GMP/GDP).

Responsibilities

• Inspect and test biological raw materials and intermediates per procedures.
• Perform sampling, results review, and visual inspection per established procedures.
• Enter results into ERP and LIMS as required.
• Recognize and investigate out of specification or out of trend results and report to supervisor.
• Assist with testing improvements and changes within change management.
• Follow good laboratory practices and procedures.

Skills

Time management

Analytical skills

Teamwork

Education

Bachelor’s degree or equivalent in life science

Tools

Laboratory instruments

Job description

Bio-Rad Laboratories in Irvine, CA is seeking a Quality Control Specialist I to inspect and test biological raw materials and intermediates, perform sampling, review results, and log data into ERP and LIMS per established procedures.

You will identify out-of-spec or out-of-trend results, assist with testing improvements within change management, and work closely with a team while following GMP/GDP and good laboratory practices to ensure product quality.