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Quality Assurance Specialist

$60k - $70k

NPAworldwide

Quality Assurance SpecialistNPAworldwide Recruitment NetworkLocation: Lafayette, 47905, IN, Indiana, USARemote Status: no remoteEmployment Type: Full Time/Direct HireCompensation: 60000-70000 / US Dollars / Annual SalaryRequisition: OOJ - 49499Visa sponsorship provided: NoOccupational Categories: Healthcare/ Medical/ Therapy/ Social ServicesIndustries: Healthcare / Medical,Pharmaceutical,Research & Development ServicesJob DescriptionReview and approve deviations, CAPA, and change controls.Participate in client audits and regulatory inspections.Ensure quality systems comply with company procedures and applicable regulatory expectations.Train staff and key personnel on company procedures, SOPs, and current industry requirements.Support product validations and designs.Review and audit scientific reports for accuracy, completeness, and compliance.Conduct internal quality audits.Evaluate the impact of new products or changes to existing products on regulatory applications.Apply established SOPs to daily activities.Collaborate with project teams to achieve quality and organizational objectives.Support ongoing quality improvement and regulatory compliance initiatives.Perform other duties as assigned.QualificationsFamiliarity with cGMP or other applicable regulatory requirements.Strong written and verbal communication skills.Strong computer proficiency and documentation skills.Ability to manage multiple priorities and work effectively under pressure.Strong teamwork and collaboration skills.Ability to motivate and work effectively with colleagues.Ability to understand and generalize experimental design.Ability to clearly communicate scientific ideas, research findings, and conclusions.Why is This a Great OpportunityReview and approve deviations, CAPA, and change controls.Participate in client audits and regulatory inspections.Ensure quality systems comply with company procedures and applicable regulatory expectations.Train staff and key personnel on company procedures, SOPs, and current industry requirements.Support product validations and designs.Review and audit scientific reports for accuracy, completeness, and compliance.Conduct internal quality audits.Evaluate the impact of new products or changes to existing products on regulatory applications.Apply established SOPs to daily activities.Collaborate with project teams to achieve quality and organizational objectives.Support ongoing quality improvement and regulatory compliance initiatives.Perform other duties as assigned.

Vacancy posted 4 days ago
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