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Quality Control Specialist
Careers Integrated Resources Inc
San Diego, CA (Onsite)
Contractor
Job Title: Quality Control Specialist
Location: San Diego, CA 92130
Contract: 5 months+ (Possible of extension)
Shift: 8 AM - 4:30 (Monday - Friday)
Pay Range: $28/hr. on W2
Job Description Summary:
The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC Associate I will prioritize daily workload and work independently. They will participate in the review of data, report results, and complete all required documentation and database entries. QC Associate I will receive specific instructions and ongoing guidance regarding required tasks and expected results.
Must have:
Essential Responsibilities:
• Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting.
• This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues.
• Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures.
• Will prioritize daily workload and develop skills to work independently.
• Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures.
• Calibrate and maintain equipment. Report problems to QC Supervisor or Manager.
• Maintain logs and required documentation, as necessary.
• Prepare lab supplies, reagents, and assist with laboratory maintenance, as needed.
• Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment.
• Participate in Environmental, Health & Safety programs.
• Address corrective actions whenever a hazard is identified.
• Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
• Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements.
• Participate in group or intra-department teams and projects as required.
• Participate in assigned cross-training.
• Perform other related duties and assignments, as required.
Qualifications/Experience:
• BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years related experience in a biotech lab environment.
• Experience in an industrial or research laboratory preferred.
• Flow Cytometry experience required and Tissue Culture experience highly preferred.
Skills:
• Basic computer skills: MS Excel & Word.
• Knowledge of general laboratory safety.
• Effective interpersonal, written and oral communication skills.
• Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs.
• Effective analytical and problem-solving skills.
#sczr2
Location: San Diego, CA 92130
Contract: 5 months+ (Possible of extension)
Shift: 8 AM - 4:30 (Monday - Friday)
Pay Range: $28/hr. on W2
Job Description Summary:
The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC Associate I will prioritize daily workload and work independently. They will participate in the review of data, report results, and complete all required documentation and database entries. QC Associate I will receive specific instructions and ongoing guidance regarding required tasks and expected results.
Must have:
- BA/BS degree in a related scientific discipline or some related college coursework with a minimum of 2 years’ experience in a biotech lab environment.
Essential Responsibilities:
• Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting.
• This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues.
• Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures.
• Will prioritize daily workload and develop skills to work independently.
• Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures.
• Calibrate and maintain equipment. Report problems to QC Supervisor or Manager.
• Maintain logs and required documentation, as necessary.
• Prepare lab supplies, reagents, and assist with laboratory maintenance, as needed.
• Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment.
• Participate in Environmental, Health & Safety programs.
• Address corrective actions whenever a hazard is identified.
• Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
• Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements.
• Participate in group or intra-department teams and projects as required.
• Participate in assigned cross-training.
• Perform other related duties and assignments, as required.
Qualifications/Experience:
• BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years related experience in a biotech lab environment.
• Experience in an industrial or research laboratory preferred.
• Flow Cytometry experience required and Tissue Culture experience highly preferred.
Skills:
• Basic computer skills: MS Excel & Word.
• Knowledge of general laboratory safety.
• Effective interpersonal, written and oral communication skills.
• Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs.
• Effective analytical and problem-solving skills.
#sczr2
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