VP, Global Quality - Development and Manufacturing at Jobgether – United States

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a VP, Global Quality - Development and Manufacturing in United States.

This is a senior global leadership role responsible for defining and driving quality strategy across development and manufacturing operations in a highly regulated pharmaceutical services environment. You will oversee global quality assurance, regulatory compliance, quality control, and GxP systems across multiple international sites. The role ensures that all products meet the highest standards of safety, efficacy, and regulatory compliance across global markets including the US, EU, and ROW. You will act as a key advisor on quality and regulatory strategy for sterile drug development, including formulation, filling, and packaging operations. This position plays a critical role in maintaining inspection readiness, strengthening compliance culture, and enabling sustainable business growth. It is ideal for a seasoned quality leader with deep experience in sterile pharmaceutical manufacturing and global regulatory environments.

• Lead the global Quality and Regulatory Affairs strategy for the Development and Manufacturing segment, defining objectives, priorities, and long-term quality goals.
• Ensure full compliance with global GMP standards and regulatory requirements across all sites, including US, EU, and international markets.
• Oversee quality systems, KPIs, and performance metrics through Quality Management Reviews, ensuring consistent operational excellence.
• Drive continuous improvement initiatives to strengthen quality culture, reduce risk, and enhance operational performance across global facilities.
• Maintain inspection readiness across all D&M sites and support regulatory inspections, audits, and remediation activities.
• Partner with Business Development and Operations teams to support client engagements, technical feasibility assessments, and commercial opportunities.
• Collaborate with site leadership teams to identify compliance risks and implement effective remediation strategies.
• Provide leadership on training programs to ensure strong understanding and execution of GMP and quality standards across the organization.
• Contribute to global strategic decisions as part of the D&M leadership team, influencing operational and commercial direction.
• Develop and standardize global quality documentation frameworks to ensure alignment across all sites and functions.

• Bachelor’s degree in a relevant scientific or technical discipline required; advanced degree strongly preferred.
• 15+ years of experience leading global quality organizations in pharmaceutical or biotech development and manufacturing.
• At least 10+ years of experience in sterile drug product manufacturing, including formulation, filling, and packaging.
• Strong expertise in GMP compliance and global regulatory environments across North America and Europe.
• Experience with sterile dosage forms such as vials, syringes, cartridges, liquid, and lyophilized products.
• Proven leadership in managing cross-functional, multi-site global teams in highly regulated environments.
• Strong ability to partner with Operations, Business Development, and technical teams to drive business and quality outcomes.
• Excellent communication, leadership, and stakeholder management skills at executive level.
• Ability to manage complex regulatory landscapes and ensure inspection readiness at all times.
• Medical device experience is a plus, as well as exposure to cross-functional manufacturing environments.
• Willingness to travel up to 50% globally.

• Competitive executive compensation aligned with global leadership responsibility
• Opportunity to lead global quality strategy across multiple international manufacturing sites
• Strong focus on professional growth, leadership development, and continuous learning
• Collaborative and purpose-driven culture focused on improving patient outcomes
• Exposure to cutting-edge sterile pharmaceutical manufacturing and global regulatory frameworks
• Inclusive workplace culture emphasizing equity, diversity, and belonging
• Opportunity to influence enterprise-wide quality systems and strategic direction
• Work within a global organization supporting life-changing therapies for patients worldwide.