Gcp auditor jobs in United States

The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance and ensure GXP compliance with regulatory authorities. · ...

JOB DESCRIPTION: · The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting qualit ...

+Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials+ · +Perform clinical vendor audits along with various SMEs (IRT, EDC etc.) to comprehensively assess all services provided by a vendor+ · +Review, understand, and audit clini ...

· Job Description: · The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting qua ...

JOB DESCRIPTION: The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting quality ...

· JOB DESCRIPTION: · The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting qua ...

The GCP Quality Assurance Auditor will report to the Director and ensure GXP compliance with regulatory authorities. · Plan and conduct scheduled global clinical process audits. · Develop audit reports and distribute them to stakeholders. · Review clinical related regulations and ...

The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. · This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting quality management syst ...

The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities. The incumbent will conduct and or participate in all GXP QA audit programs which include both interna ...

The GCP Quality Assurance Auditor will report to the Director and ensure compliance with regulatory authorities. · The incumbent will conduct audits and provide day-to-day support to the GXP QA Director in clinical operations/Non-clinical and Manufacturing. · This position requir ...

Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials. · ...

Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials. · ...

· OB DESCRIPTION: · The GCP Quality Assurance Sr. Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Companys compliance directives and supporting q ...

The GCP Quality Assurance Sr. Auditor will report to the Director the GCP/PVG Quality Assurance. · Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials. · ...

This position focuses on ensuring GXP compliance with regulatory authorities driving and implementing compliance directives and supporting quality management systems to minimize risks in a regulated pharmaceutical environment. · Plan and conduct scheduled global clinical process ...

Location: Paramus, New Jersey (Hybrid: 3 days onsite Tuesday to Thursday) · Education: Bachelor's Degree in Scientific, Healthcare, or Related Field · Experience: Minimum 5+ years in the Pharmaceutical or Biopharmaceutical Industry · Travel: Up to 10% · About the Opportunity · Jo ...

We need experienced industry professionals to join our Quality Assurance (QA) team. · This position will support and audit global trials in a variety of therapeutic areas, · maintaining organizational and regulatory standards throughout our company. ...

Due to our rapid growth we need experienced industry professionals to join our Quality Assurance (QA) team. This position will support and audit global trials in a variety of therapeutic areas maintaining organizational and regulatory standards throughout our company. · ...

Details for the position are as follows: · Work Location: Rahway, NJ - Hybrid · Hybrid schedule: 3 days onsite — Tuesday and Wednesday are core in-office days, with the option to work onsite either Monday or Thursday for the third day. · 22-month contract to start with the possi ...

Due to rapid growth need experienced industry professionals join Quality Assurance QA team. This position will support and audit global trials in variety therapeutic areas maintaining organizational and regulatory standards throughout company. · ...