GCP Senior Auditor

Bryce Poynt Consulting; Paramus (NJ); On-site; USD 90,000 - 120,000; Full time

Job summary

A rapidly growing biopharmaceutical company in Northern New Jersey is seeking a GCP Quality Assurance Sr. Auditor. This role involves ensuring GXP compliance, conducting audits, and supporting quality management systems in a regulated pharmaceutical environment. The ideal candidate will have extensive GCP experience and be on-site in Paramus.

Qualifications

• 5+ years of pharmaceutical experience.
• Intensive GCP and safety background.

Responsibilities

• Plan and conduct global clinical process and clinical vendor audits.
• Develop audit reports and distribute them to stakeholders.
• Support regulatory agency inspections.

Skills

GCP

Quality Assurance

Audit

Education

BS degree in scientific, health care or related discipline

Job 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 quality management systems to ensure compliance and minimize risk in a regulated pharmaceutical environment. The incumbent will conduct and or participate in all GXP QA audit programs which include both internal and external GXP audits. This position will provide day to day support to the GXP QA Director in clinical operations / Non-clinical and Manufacturing to manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
• The Sr. Auditor of Quality Assurance will work with the QA and cross functional teams, communicate with QA consultants and has contact with external auditees, vendors, partners and affiliates. The ideal candidate will have extensive GCP experience.
• This opportunity is with a rapidly growing biopharmaceutical company that specializes in Neurology and Psychiatry therapies. They are based in Northern New Jersey and require the candidate to be on-site. Performs and manages all types of audits in the audit program of Clinical Development and Safety Pharmacovigilance

RESPONSIBILITIES :

• Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials.
• Plan and conduct audits of specific clinical processes based on risk.
• Perform clinical vendor audits along with various SMEs (IRT, EDC etc.) to comprehensively assess all services provided by a vendor.
• Develop audit reports and distribute them to appropriate stakeholders.
• Own and manage related clinical vendor non-conformances.
• Review, understand, and audit clinical related regulations and guidelines (e.g. FDA regs, GCP, etc.).
• Collaborate with clinical sourcing, supplier quality and clinical partnership to manage clinical vendors.
• Support the preparation, coordination, and participation of regulatory agency inspections.
• Participate in and support quality improvement projects.

QUALIFICATIONS :

• 5+ years of pharmaceutical experience
• BS degree in scientific, health care or related discipline
• Intensive GCP and safety background
• Experience with both internal and external process and systems audits
• Strong knowledge of development policies, procedures and standards (SOPs, QMS)
• Ability to work with global clinical teams in developing objectives for audits of clinical studies
• 10% Traveling required

Working Place :

Paramus, New Jersey, United States

Create a job alert for this search