Quality Assurance Auditor | cGMP | FDA - Masis Staffing
Masis Professional Group
Quality Assurance Auditor | cGMP | FDAJoin an industry-leading health and wellness manufacturer dedicated to improving lives through science, innovation, and uncompromising quality. With a strong reputation for excellence, the company develops trusted products backed by research and produced to the highest standards of quality and compliance.Employees enjoy a collaborative, values-driven culture that emphasizes integrity, continuous improvement, professional growth, and making a meaningful impact every day. If you're looking to join a mission-focused organization where quality matters and people are valued, you'll feel right at home here!The Supplier Quality Specialist – Audits & ComplianceReports to the Supplier Quality and Compliance Manager. This role is responsible for developing and maintaining a strong Internal Compliance program ensuring compliance to applicable regulations. The Supplier Quality Specialist is required to perform internal and external audits, prioritize audit schedules and corrective actions to the findings identified.Must haves:Must have a minimum of 5 years of Quality Assurance auditing experience in cGMP environment with a minimum of 5 years of external vendor/supplier compliance auditing experience within an FDA regulated industry.Experience with 21 CFR Parts 210, 211 and 21 CFR 111ASQ Certified Auditor (CQA) Certification is preferred.Must be proficient in Computer Software applications including MS office suite.Must be able to travel 20 – 30% for domestic audits, (International travel may be needed per quality management).What you'll do:Plan, schedule, and conduct internal and external audits to ensure regulatory and quality compliance.Audit suppliers and contract manufacturers (CMOs) and maintain vendor qualification programs.Manage supplier corrective actions (SCARs) and verify effective CAPA implementation.Assess audit findings, determine risk levels, and drive corrective and preventive actions.Maintain audit, supplier, and compliance documentation within the Quality Management System (QMS).Monitor and report audit and compliance metrics to management.Train and support cross-functional teams on quality and compliance requirements.Identify compliance risks and support process improvements to mitigate risk.Support regulatory inspection readiness and ongoing compliance initiatives.Utilize SAP and electronic quality systems to support Quality Assurance activities.Preferred:ASQ Certified Quality Auditor (CQA) preferred.SAP and Quality Management System experienceOutstanding Benefits & Relocation Package! • 45 Days of Fully Furnished Temporary Housing • $5,000 Relocation Stipend • Paid Area Exploration Visits • Weekly Pay • Christmas Eve–New Year's Shutdown • Up to $5,000 Annual Tuition Reimbursement • Gym/Fitness Reimbursement • Company-Paid Life Insurance • Company-Paid Short-Term Disability • Employee Assistance Program (EAP) • Annual HSA Contribution • Daycare & Private School Tuition AssistanceA company that truly invests in its employees and their families! Masis Professional Group
- ...understand and comply with Quality and Compliance... ...to other Quality Assurance team members.... ...auditing experience in cGMP environment with a... ...within an FDA regulated industry... ...required.ASQ Certified Auditor (CQA)... ...Science or Technical field required. MDS StaffingSuggestedContract workTemporary work
- Lancaster, SCDescriptionThe Quality Assurance Auditor reports to the Supplier Quality and Compliance Manager... ...Assurance auditing experience in cGMP environment with a minimum of 5 years of... ...compliance auditing experience within an FDA regulated industry.Knowledge of the...SuggestedContract workTemporary work
- ...Career Move Starts Here! The Role: Quality Assurance Auditor Location: Lancaster, SC... ...~5 years of QA auditing experience in a cGMP environment & external vendor/supplier compliance within an FDA regulated industry. ~ Knowledge of Regulations...SuggestedFull timeContract work
- ...Quality Assurance Auditor Lancaster, SC This role is responsible for developing and maintaining a strong Internal Compliance program ensuring compliance to applicable regulations. The QA Inspector is required to perform internal and external audits, prioritize audit...Suggested
- ...Quality Assurance SpecialistThe Quality Assurance Specialist is responsible for the daily Quality Assurance support in the Manufacturing and... ...correction of deficiencies found within the documentation review per cGMP, Nutramax SOPs, Contract Manufacturing Organization (SOPs),...SuggestedContract workFlexible hours
- Nutramax Laboratories, Inc. is seeking a Quality Assurance Specialist to support on-site QA in Manufacturing and Packaging and related GMP functions... ...department and CMO activities. Ideal candidates have strong cGMP knowledge, attention to detail, and the ability to work...
- ..., a commitment to patient safety, and a drive to turn data and insights into meaningful improvements? Join our team as a Part-Time Quality Management Specialist, RN, and help shape a culture where quality, safety, and exceptional patient experiences come first. Entity...Part timeReliefShift work
- ...available. We are partnering with a growing pharmaceutical, consumer health, and animal health manufacturer to appoint a Vice President of Quality. This role reports to the President & CEO and will own the entire Quality function, including QA, QC, compliance, and regulatory...Relocation package
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