Associate Director, GCP QA

Mirum Pharmaceuticals, Inc.; Foster City (CA); On-site; USD 190,000 - 205,000; Full time

Job summary

Mirum Pharmaceuticals, Inc. is seeking an Associate Director of GCP/GVP/GLP-QA to support clinical study programs by managing GCP quality assurance. The ideal candidate will have 10-12 years of pharmaceutical experience, including supervising GCP Quality staff and deep knowledge of GCP regulations.

This role includes responsibilities such as managing QA readiness activities, supporting internal audits, and providing quality oversight for GCP activities. The salary range for this position is $190,000 to $205,000 USD, excluding bonuses and benefits.

Qualifications

• 10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality.
• 5+ years supervising GCP Quality internal staff and/or external consultants.
• Knowledge of EMA EudraLex Regulations and ICH Guidelines.

Responsibilities

• Achieve established timelines for deliverables.
• QA Representative for assigned Mirum’s Program’s Clinical Study Management Teams.
• Manage/Support BIMO inspection readiness activities.
• Support GCP/GCLP/GVP internal audits.

Skills

Strong verbal and written communication

Knowledge of GCP regulations

Knowledge of FDA Regulations

Knowledge of GVP regulations

Education

Bachelor’s Degree in a scientific discipline

Job description

Mission

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.

Position Summary

The Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum’s clinical study programs as the GCP-QA representative on the study management team; managing activities involving GCP quality assurance and compliance with applicable regulatory requirements; development and implementation of policies and procedures to ensure quality standards in compliance with relevant regulatory and quality guidelines. Additionally, this position will support GVP and GLP QA operational activities to ensure data integrity and meeting regulatory expectations and industry standards. This position requires experience with global contract research organizations (CROs) and GCP Vendors as well as knowledge of global GCP regulations.

Job Functions / Responsibilities

• Achieve established timelines for deliverables.
• QA Representative for assigned Mirum’s Program’s Clinical Study Management Teams.
• Manage/Support BIMO inspection readiness activities.
• Support GCP/GCLP/GVP internal audits.
• Provide quality oversight for the GCP/GVP/GLP vendor activities, including internal/external deviations, CAPAs, change controls, and KPIs/KQIs.
• Support GCP, GCLP and GVP Vendor Management/Audit Program. Ad hoc audits may be requested.
• Assist with planning and supporting Clinical Site Management/Audit Program. Ad hoc site audits may be requested.
• Assist with and support regulatory agency inspections for the GCP and PV impacted functions.
• Provide GCP/GCLP/GVP Training as necessary.
• Support Quality Management Team (QMT) by providing monthly/quarterly updates based on role and responsibilities.
• Support process improvement of QA department, KPI/QPI tracking and oversight.
• Manage GCP/GVP/GLP consultant(s) as needed.

Qualifications

Education / Experience

• Bachelor’s Degree in a scientific discipline.
• 10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality and 5+ years supervising GCP Quality internal staff and/or external consultants.
• Knowledge and demonstrated experience in the applicable GCP regulations, FDA Regulations and Good Clinical Practices, EMA EudraLex Regulations, and ICH Guidelines.
• Strong verbal and written communication.
• Knowledge of basic GVP, GCLP and GLP regulations.

The salary range for this position is $190,000 to $205,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.

Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.

Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.