Overview
VP OPERATIONS, VACCINES Jobs in Riyadh, Saudi Arabia at NStarts International Talents Group Company Limited
Title: VP OPERATIONS, VACCINES
Company: NStarts International Talents Group Company Limited
Location: Riyadh, Saudi Arabia
Job Description: VP OPERATIONS, VACCINES
Location：Riyadh, Saudi Arabia
Key Responsibilities
Strategic Facility Development
 Lead all aspects of design, construction, commissioning, and validation of two fully
segregated GMP-compliant vaccine manufacturing facilities .
 Oversee procurement and qualification of process and utility equipment in alignment
with best practices and regulatory expectations.
 Develop and implement project timelines, budgets, and performance KPIs in
collaboration with the executive leadership team.
Operations Leadership
 Build and lead an integrated site organization encompassing manufacturing, quality,
supply chain, engineering, EHS, regulatory affairs, and site administration.
 Define and drive the site’s operational readiness strategy, including batch execution
systems, QA/QC labs, warehouse, and cleanroom operations.
 Serve as the ultimate site authority for execution of clinical and commercial GMP
vaccine production across all platforms.
Technology Transfer and CMC
 Direct all aspects of technology transfer from international licensors into the new
facility, ensuring full CMC package compliance.
 Lead process scale-up, process validation, and regulatory filing support in
collaboration with technical and regulatory affairs teams.
Regulatory Compliance & Quality Systems
 Ensure full compliance with WHO PQ, EMA, SFDA, and other applicable regulatory
standards for both human and veterinary vaccine manufacturing.
 Oversee the implementation of quality systems, documentation practices, CAPA
management, and audit readiness.
Organizational Development & Talent Acquisition
 Lead the recruitment and development of a high-performing site team across all
functions.
Required Qualifications:
 25+ years of leadership experience in global vaccine manufacturing, with direct
experience across both human and animal vaccine platforms.
 Proven track record in designing, building, and operationalizing a GMP
biopharmaceutical manufacturing facility.
 In-depth knowledge of vaccine CMC, aseptic manufacturing, formulation and fillfinish processes, and biologics regulatory frameworks.
 Strong expertise in technology transfer, scale-up, process validation, and quality
management systems.
 Demonstrated ability to lead multi-disciplinary teams and manage complex capital
projects.
 Excellent understanding of international GMP regulations (EU, US, WHO, SFDA)
applicable to vaccines for animal and for human use.
 Strong interpersonal, communication, and stakeholder engagement skills.
 Fluency in English is required; Arabic is a plus
How to Apply：
Email：[email protected]
Whatsapp：+86 16620851102
Wechat：Nancyyyyy2568
Linkedin：https://www.linkedin.com/in/%E6%99%A8%E6%B1%90-%E9%83%9D-23761a300/
