Quality Assurance
katalyst croSaint Paul, MN
Quality Assurance
katalyst croSaint Paul, MNSenior L5
Quality Control Systems ManagersQuality Control AnalystsInspectors, Testers, Sorters, Samplers, and Weighers
Pharmaceutical Preparation ManufacturingBiological Product ManufacturingIn-Vitro Diagnostic Substance Manufacturing
APPLY NOW (opens in a new tab)Job Description:
We are looking for a Quality Operations QA Specialist to support daily quality assurance activities at our client site in Morris Plains, NJ. The candidate will ensure that manufacturing, packaging, and testing operations comply with cGMP and company quality standards.
Responsibilities:
Perform QA review of batch records, deviations, CAPAs, and change controls. Provide quality support to manufacturing, packaging, and laboratory operations. Ensure compliance with GMP, FDA, and company quality policies. Participate in investigations and support root cause analysis for quality issues. Review and approve SOPs, validation protocols, and reports. Support internal and external audits and inspection readiness. Maintain accurate QA documentation and records.
Requirements:
Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field. 35 years of experience in Quality Assurance or Quality Operations. Background in Pharma or Healthcare industry is required. Strong understanding of GMP, FDA, and quality systems. Good communication and documentation skills.
Nice To Have:
Experience with Track Wise, Veeva, or other electronic quality systems. Knowledge of aseptic or sterile manufacturing processes.
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Level
Senior L5
Location
Saint Paul, MN
Occupation
Quality Control Systems Managers
Industry
Pharmaceutical Preparation Manufacturing
Posted
today