Quality Assurance
Our expert quality recruiters are standing by to discuss your quality assurance and quality management hiring needs
Quality in the Medical Device, Pharmaceutical and Biotech industries requires specific industry knowledge and expertise. Finding candidates with the combination of quality assurance and therapeutic/industry expertise can create a challenge. Having worked with candidates with quality backgrounds at all levels our quality recruiters understand the nuance of expertise which includes:
Vice President Quality
Vice President Global Quality
Director of Quality
Director, Post Market Surveillance and Vigilance
Quality Control Manager
Quality Supervisor Vigilance MDR
Quality Control Manager
Quality Supervisor Vigilance MDR
Senior Quality Assurance Specialist
Senior Quality Control Technologist
Quality Assurance Engineer
Quality Assurance Complaints Analyst
Supplier Quality Manager
Vice President Quality and Regulatory
Quality and Regulatory Director
Director of Quality Systems
Senior Manager Quality Management
Manager Quality Operations
Senior Manager Quality Management
Manager Quality Operations
Quality Assurance Supervisor
Senior Quality Engineer
Quality Engineer
Principle Quality Administrator
Quality Analyst
Supplier Quality Engineer
EXPERTISE
AREAS
CAPA AND ROOT CAUSE ANALYSIS | CFR PART 11 | COMPLIANCE ACTIVITIES, DEVELOPMENT OF COMPLIANCE PROGRAMS, FACILITY AUDITS FOR ADHERENCE TO GLP AND GMP STANDARDS | GMP, GCP, CVP, GVP, GSCVP, GLP, GCLP | COMPLAINTS, CAPA, AE PROCESS AND SYSTEMS | FDA WARNING LETTER REVIEW, RESPONSE, AND MITIGATION | ISO13485 | LABELING, CONSISTENCY AND ACCURACY | QMS SELECTION, DESIGN AND IMPLEMENTATION | QUALITY AUDITS AND MOCK INSPECTIONS | SOP DEVELOPMENT | SUPPLIER QUALITY AUDITS | MEDICAL DEVICE SINGLE AUDIT PROGRAM (MDSAP) | PREPARATION, REVIEW, MANAGEMENT AND FILING OF SUBMISSIONS WORLDWIDE IN COMMON TECHNICAL DOCUMENT (CTD/ECTD) FORMAT | PRE-INDS, INDS, CTAS, BLA, NDAS, NDSS, MAAS, 510(K)S, PMAS, IMPDS, PRE-SUBMISSION BRIEFING DOCUMENTS, INVESTIGATOR’S BROCHURES, ANNUAL REPORTS, INTEGRATED SUMMARIES, ETC. | SCIENTIFIC WRITING OF NONCLINICAL DATA (SAFETY), CLINICAL DATA, AND PREPARATION OF CMC DOCUMENTS | NONCLINICAL PROGRAMS AND QUALITY (CMC) COMPONENTS, AND CLINICAL PROGRAMS TO SUPPORT REGISTRATIONS WORLDWIDE
