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

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