QA Manager, GCP

About the role

Due to the hybrid nature of the job, candidates must reside within commuting distance to San Diego, CA or be willing to relocate to San Diego, CA. The QA Manager, GCP is responsible for ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area, providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi, including audits, inspections, and risk assessment of BLA/NDA/IND/CTA submissions under the global umbrella. This role supports the collection of the data needed for Audit program risk assessment, supports clinical studies-related activities from a quality perspective across Sobi, ensures qualification of global and local ESP, as applicable, in GCP-regulated areas per Sobi procedures, and works with relevant stakeholders across the Sobi organization.

Key Responsibilities

• Ensure GCP audit management excellence of the end-to-end audit management process and overview of the assigned audits, as planned
• Assess and approve from quality perspective the GCP deviations (global and local, as applicable), GCP related CAPAs
• Prepare regular status report on performed audits, audit trending, deviation trending, CAPAs trending and agreed upon metrics to ensure Quality oversight
• Contribute and support the GCP audit risk assessment according to SOPs
• Ensure active contribution in the cross-functional team with procurement, business owners for GxP and Quality requirements and documented qualification of GCP service providers and review provisions in contracts/Quality agreements, as applicable
• Act as QA representative during GCP inspections at global and site level, as applicable, and contribute to the Inspection Readiness framework and promote continuously quality mindset across Sobi
• Author GCP QA related processes, review and give guidance under global umbrella

Qualifications

Required:

• University degree or similar in Life Sciences or related discipline
• 5+ years of pharmaceutical industry experience in Clinical Quality Assurance or in the operational conduct of clinical trials and the application of GCP audit and/or Quality Assurance experience

Technical Skills

• Excellent knowhow of the applicable ICH GCP guidelines, industry best practices and FDA, EMA and ROW regulatory requirements
• Quality assurance activities principles and know-how
• Documented education/experience in QA systems and preferably auditing

Soft Skills

• Structured with focus on results and detail oriented
• Strong interpersonal skills with communicative and flexible attitude
• Proactive and collaborative mindset
• Strong multi-tasking abilities with high resilience at stress and adaptive skills

Pay

The base salary range for this role is $112,000-$153,000. Each individual offer will be determined based on several factors, including your experience, qualifications, and location. Additionally, this role is eligible for both short-term and long-term bonuses, as outlined in the plan details.