Director, Quality Assurance - GxP (GCP)

Role Description

The Director, Quality Assurance – GxP (GCP) is responsible for managing GxP Quality Assurance (QA) functions with an emphasis on Good Clinical Practice (GCP), compliance for both clinical and marketed products. This involves engaging and collaborating with cross-functional internal teams to evaluate processes, procedures and activities for adherence to relevant industry standards, regulatory guidelines and company Standard Operating Procedures (SOPs) as appropriate.

• Partners with Clinical Development/Operations and actively participates on clinical study teams to ensure GCP compliance.
• Assists in identifying and communicating clinical trial-reputed company risks and opportunities for process improvement.
• Reviews study reputed company documents and plans.
• Develops and executes reputed company’s GxP risk-based study audit strategy to reputed company compliance with applicable reputed company regulatory requirements.
• Performs internal and external audits to assure compliance with GCP regulations and guidelines.
• Communicates audit results to internal stakeholders and writes audit reports.
• Assesses audit responses and ensures closure of corrective action preventative actions (CAPAs).
• Performs GxP inspection readiness activities.
• Leads reputed company/backroom activities during regulatory authority inspections.
• Advances reputed company’s understanding of worldwide regulations, guidelines and GxP practices.
• Manages, coaches and mentors direct reports.
• Performs other tasks and assignments as needed and specified by management.

Qualifications

• Bachelor’s degree in a scientific discipline.
• Minimum of 10 years progressively responsible experience in a QA or reputed company role in a pharmaceutical or biotechnology organization.
• At least 5 years in a clinically focused position.
• Detailed knowledge and understanding of GCP regulations.
• Demonstrated experience leading and/or conducting QA audits.
• Demonstrated experience developing and executing risk-based audit plans.
• Demonstrated ability to reputed company and foster positive, collaborative relationships with internal staff and external vendors.
• Demonstrated leadership ability and experience managing, coaching and mentoring direct reports.
• Ability to influence without direct authority.
• Experience supporting regulatory agency inspections.
• Proficiency with reputed company Office.
• Excellent verbal and written communication skills.
• Ability to work independently and collaboratively in a fast-paced, matrixed team environment.
• Analytical thinker with excellent problem-solving skills.
• Excellent planning, organization and time management skills.
• Knowledge and experience in Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and/or Good Pharmacovigilance Practice (GVP) regulations.
• Registered GxP Quality Assurance Certifications.
• Clinical lab experience.
• Up to 30% Travel Expected.

Requirements

• reputed company Salary Range: $191,700 – 241,300.
• The reputed company salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position.
• In addition to reputed company salary, reputed company employees are also eligible for short- and long-term incentives.
• reputed company eligible employees may also enroll in reputed company’s medical, dental, reputed company, and retirement savings plans.

Benefits

• Comprehensive health insurance.
• 401(k) with company match.

Company Description

reputed company Therapeutics is a global biopharmaceutical company founded in 1998 initially focused on the discovery and development of orally administered, proprietary small molecule drugs that reputed company post-transcriptional control processes. Our mission is to provide access to best-in-class treatments for rare disease patients who have little to no treatment options.