Meet Life Sciences
Director GCP, Quality Assurance
Meet Life Sciences, South San Francisco, California, us, 94083
Base pay range
$210,000.00/yr - $240,000.00/yr I’m partnering with a clinical-stage biotechnology company developing first-in-class antibody therapies that target signal regulatory proteins (SIRP) for the treatment of severe immunological diseases and cancer . They’re seeking a
Director, GCP Quality Assurance (QA)
to lead their global GCP and Pharmacovigilance (PV) quality strategy and play a critical role in ensuring patient safety, regulatory compliance, and inspection readiness across all phases of clinical development. Responsibilities
Drive the company’s GCP and PV quality strategy across all phases of clinical development Lead risk-based audit programs for sites, vendors, and internal processes Prepare for and manage global regulatory inspections (FDA, EMA, MHRA, PMDA) Partner with Clinical Development, Operations, PV, and Regulatory to enable compliant trial execution and vendor oversight Oversee GCP/PV audits, CAPA management, and continuous quality improvements Shape quality systems, SOPs, and policies to support inspection readiness and operational excellence. Qualifications
Bachelor’s or advanced degree in a scientific discipline (Biology, Chemistry, Chemical Engineering, etc.) 10+ years of biopharma industry experience with a strong focus on GCP QA Direct experience with global regulatory inspections (FDA, EMA, MHRA, PMDA) If interested, apply now or contact Kelly Komon: Kelly.Komon@meetlifesciences.com Benefits provided by Meet Recruitment Equal Opportunity Employer:
Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where in operation. Seniority level
Director Employment type
Full-time Job function
Quality Assurance Industries
Biotechnology Research and Pharmaceutical Manufacturing
#J-18808-Ljbffr
$210,000.00/yr - $240,000.00/yr I’m partnering with a clinical-stage biotechnology company developing first-in-class antibody therapies that target signal regulatory proteins (SIRP) for the treatment of severe immunological diseases and cancer . They’re seeking a
Director, GCP Quality Assurance (QA)
to lead their global GCP and Pharmacovigilance (PV) quality strategy and play a critical role in ensuring patient safety, regulatory compliance, and inspection readiness across all phases of clinical development. Responsibilities
Drive the company’s GCP and PV quality strategy across all phases of clinical development Lead risk-based audit programs for sites, vendors, and internal processes Prepare for and manage global regulatory inspections (FDA, EMA, MHRA, PMDA) Partner with Clinical Development, Operations, PV, and Regulatory to enable compliant trial execution and vendor oversight Oversee GCP/PV audits, CAPA management, and continuous quality improvements Shape quality systems, SOPs, and policies to support inspection readiness and operational excellence. Qualifications
Bachelor’s or advanced degree in a scientific discipline (Biology, Chemistry, Chemical Engineering, etc.) 10+ years of biopharma industry experience with a strong focus on GCP QA Direct experience with global regulatory inspections (FDA, EMA, MHRA, PMDA) If interested, apply now or contact Kelly Komon: Kelly.Komon@meetlifesciences.com Benefits provided by Meet Recruitment Equal Opportunity Employer:
Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where in operation. Seniority level
Director Employment type
Full-time Job function
Quality Assurance Industries
Biotechnology Research and Pharmaceutical Manufacturing
#J-18808-Ljbffr