Our client a world leader in biotechnology and life sciences is looking for a "QC Analyst I" based out of Oceanside CA.
Job Duration: Long Term Contract (Possibility Of Extension)
Pay Rate : $25/hr on W2
We are seeking a detail-oriented QC Analyst to perform routine and non-routine testing of manufacturing environments and in-process products. This role is responsible for data collection analysis and reporting ensuring compliance with cGMP GLP and GDP standards to maintain product quality and safety.
Key Responsibilities :
Conduct microbiological and chemical testing per established SOPs.
Collect analyze and report data ensuring accuracy and compliance.
Review results for conformance to specifications and investigate anomalies.
Calibrate maintain and troubleshoot laboratory equipment.
Support data trending documentation and regulatory submissions.
Collaborate with team members to complete QC testing activities.
Follow all safety environmental and quality guidelines.
Qualifications :
Bachelors degree in Life Sciences or related field.
Experience in a GMP-regulated laboratory environment preferred.
Knowledge of microbiological/chemical assays and lab instrumentation.
Strong attention to detail documentation and problem-solving skills.
If interested please send us your updated resume at
Our client a world leader in biotechnology and life sciences is looking for a "QC Analyst I" based out of Oceanside CA. Job Duration: Long Term Contract (Possibility Of Extension)Pay Rate : $25/hr on W2 We are seeking a detail-oriented QC Analyst to perform routine and non-routine testing of manufac...
Our client a world leader in biotechnology and life sciences is looking for a "QC Analyst I" based out of Oceanside CA.
Job Duration: Long Term Contract (Possibility Of Extension)
Pay Rate : $25/hr on W2
We are seeking a detail-oriented QC Analyst to perform routine and non-routine testing of manufacturing environments and in-process products. This role is responsible for data collection analysis and reporting ensuring compliance with cGMP GLP and GDP standards to maintain product quality and safety.
Key Responsibilities :
Conduct microbiological and chemical testing per established SOPs.
Collect analyze and report data ensuring accuracy and compliance.
Review results for conformance to specifications and investigate anomalies.
Calibrate maintain and troubleshoot laboratory equipment.
Support data trending documentation and regulatory submissions.
Collaborate with team members to complete QC testing activities.
Follow all safety environmental and quality guidelines.
Qualifications :
Bachelors degree in Life Sciences or related field.
Experience in a GMP-regulated laboratory environment preferred.
Knowledge of microbiological/chemical assays and lab instrumentation.
Strong attention to detail documentation and problem-solving skills.
If interested please send us your updated resume at