Planet Pharma
Flexible to work weekend/holidays when needed
Required:
Minimum of a Bachelors Degree
6 months + of experience in a GMP biotech or pharma environment
Experience with molecular skills - qPCR, flow cytometry, cell culture/cell based assay work
QC Associate I
SUMMARY: The Quality Control (QC) Associate I will contribute to general QC operation and testing in support of current Good Manufacturing Practice (cGMP) manufacturing. The individual will participate in Environmental Monitoring (EM), raw material, intermediates, drug product and stability testing program.
DUTIES AND RESPONSIBILITIES:
Perform raw material inspection and sampling.
Perform EM sampling in aseptic manufacturing environments: total particulate monitoring, active air sampling, surface and personnel monitoring.
Assist with submission of samples to contract testing laboratories.
Assist with organizing QC laboratories including equipment calibration.
Conduct QC tests for raw material, intermediates, drug product and stability samples.
Perform test following test protocols and procedures in compliance with quality standards and cGMP regulations applicable to QC laboratory.
Deliver cGMP compliant testing data and reports.
Participate in investigation of deviation or out-of-specification results in QC laboratory.
Seniority Level
Associate
Employment Type
Contract
Job Function
Other
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Required:
Minimum of a Bachelors Degree
6 months + of experience in a GMP biotech or pharma environment
Experience with molecular skills - qPCR, flow cytometry, cell culture/cell based assay work
QC Associate I
SUMMARY: The Quality Control (QC) Associate I will contribute to general QC operation and testing in support of current Good Manufacturing Practice (cGMP) manufacturing. The individual will participate in Environmental Monitoring (EM), raw material, intermediates, drug product and stability testing program.
DUTIES AND RESPONSIBILITIES:
Perform raw material inspection and sampling.
Perform EM sampling in aseptic manufacturing environments: total particulate monitoring, active air sampling, surface and personnel monitoring.
Assist with submission of samples to contract testing laboratories.
Assist with organizing QC laboratories including equipment calibration.
Conduct QC tests for raw material, intermediates, drug product and stability samples.
Perform test following test protocols and procedures in compliance with quality standards and cGMP regulations applicable to QC laboratory.
Deliver cGMP compliant testing data and reports.
Participate in investigation of deviation or out-of-specification results in QC laboratory.
Seniority Level
Associate
Employment Type
Contract
Job Function
Other
Industries
Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Planet Pharma by 2x
Get notified about new Quality Control Associate jobs in
San Diego, CA .
#J-18808-Ljbffr