The Staffing Resource Group, Inc
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Quality Control Analyst
Posted: 06/10/2025
2025-06-10
2025-07-14
Employment Type:
Contract
Division: Life Sciences
Job Number: JN -062025-20516
State: Florida
Job Description
Quality Control Analyst
Title: Quality Control Analyst Level II or Level III
Location: Gainesville, FL
Industry: Pharmaceutical
Schedule: Monday - Friday 8am - 5pm
Salary: up to $35/hr. based on experience
Employment: Contract to Hire
The Quality Control Analyst will primarily be responsible for supporting and leading early/late phase and commercial quality control activities. This highly motivated member of the Quality Unit will support the organization through the execution of activities such as raw material testing, release testing, stability testing, and environmental monitoring. As part of the Quality operations, you will be responsible for initiating and assisting in investigations and troubleshooting while adhering to cGMP and GDP practices.
Essential Duties and Responsibilities
QC Analyst II:
Required:
EOE/ADA
IND123
Title: Quality Control Analyst Level II or Level III
Location: Gainesville, FL
Industry: Pharmaceutical
Schedule: Monday - Friday 8am - 5pm
Salary: up to $35/hr. based on experience
Employment: Contract to Hire
The Quality Control Analyst will primarily be responsible for supporting and leading early/late phase and commercial quality control activities. This highly motivated member of the Quality Unit will support the organization through the execution of activities such as raw material testing, release testing, stability testing, and environmental monitoring. As part of the Quality operations, you will be responsible for initiating and assisting in investigations and troubleshooting while adhering to cGMP and GDP practices.
Essential Duties and Responsibilities
QC Analyst II:
- Actively participate in fostering a positive, collaborative work culture.
- Author and revise standard operating procedures, test methods, protocols, and reports.
- Perform execution of raw material testing, stability testing, environmental monitoring, critical utility monitoring, method qualifications, technical transfers, release testing, and method validations.
- Testing of material utilizing methods such as pH, Osmolality, Appearance, cell culture, dPCR, ELISA, and other assays used for release and characterization of products.
- Ensure QC deliverables are met in a timely manner.
- Perform data analysis and review.
- Participate in laboratory investigations including deviations and out of specifications.
- Perform equipment calibrations.
- Execute method and equipment troubleshooting and optimization, as needed.
- Maintain documentation in accordance with GDP.
- Actively participate in fostering a positive, collaborative work culture.
- Author and revise standard operating procedures, test methods, protocols, and reports.
- Lead in execution of raw material testing, stability testing, environmental monitoring, critical utility monitoring, method qualifications, technical transfers, release testing, and method validations.
- Assist in the transfer of assays from the Analytical Development Lab to the QC Lab.
- Demonstrate proficiency in flow cytometric, automated cell counting, dPCR, qPCR, ELISA-based, multiplex cytokine detection, pH, endotoxin, and cell-based assays.
- Ensure QC deliverables are met in a timely manner.
- Perform data analysis and review.
- Initiate and participate in laboratory investigations including deviations and out of specifications.
- Perform equipment calibrations.
- Execute method and equipment troubleshooting and optimization, as needed.
- Maintain documentation in accordance with GDP.
- Train and cross train QC personnel on standard operating lab procedures and test methods.
Required:
- B.S. degree in science or a life science-related field of study
- Minimum of 2+ years experience in Quality Control in a GMP environment
- Proficiency in eukaryotic cell culture, molecular techniques, operation of microscopes, and equipment calibrations (e.g., pH meters and balances)
- An equivalent combination of education and experience may be considered.
- Strong technical laboratory skills (e.g., pipetting, weighing, and measuring pH)
- Experience with writing standard operating procedures
- Familiarity with FDA, ICH, and EU Regulations and Guidelines
- Involvement in continuous improvement initiatives and laboratory investigations
- Proficiency in Microsoft Office suite applications
- Minimum of 2+ years experience in Quality Control in a GMP environment, preferably with experience in a microbiology laboratory
- Experience with the following instrumentation: flow cytometers, qPCR, digital PCR, multimode plate readers
EOE/ADA
IND123
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