Responsibilities;

1. Strategic Leadership & M&A Support:

• Represent shareholders in overseas mergers and acquisitions (M&A) projects, either through project-based assignments or direct overseas postings.
• Oversee post-investment integration, ensuring operational alignment with corporate strategy and shareholder objectives.
• Lead the operational management of overseas production bases, ensuring efficiency, compliance, and profitability.

2. Operational Excellence & Cross-functional Coordination:

• Coordinate internal (R&D, Supply Chain, Quality, Finance) and external (vendors, regulators, partners) resources to optimize production base operations.
• Ensure seamless execution of manufacturing, quality control, and supply chain processes to meet business targets.
• Drive continuous improvement initiatives to enhance productivity, cost efficiency, and compliance.

3. Compliance & Governance:

• Enforce strict adherence to international GMP standards, with a focus on injectable product manufacturing systems.
• Monitor regulatory requirements across different regions and ensure full compliance with local and international pharmaceutical regulations.
• Implement corporate governance frameworks and operational policies across overseas sites.

4. Stakeholder & Performance Management:

• Act as a key liaison between headquarters and overseas operations, ensuring clear communication and alignment.
• Lead, mentor, and develop local management teams to foster high performance and cultural integration.
• Track KPIs, prepare operational reports, and present performance updates to senior leadership.

Qualifications:

1. Experience:

• 10+ years in pharmaceutical production and operations management, including at least 2 years in overseas operations (preferably in the U.S., EU, or emerging markets).
• Proven track record in managing GMP-compliant manufacturing sites, particularly for sterile injectables.
• Experience in post-M&A integration or greenfield project setup is highly desirable.

2. Technical Expertise:

• In-depth knowledge of GMP, FDA/EMA/WHO regulations, and pharmaceutical manufacturing best practices.
• Familiarity with aseptic processing, lyophilisation, and biologics manufacturing is a plus.

3. Soft Skills & Competencies:

• Fluent in English (written and spoken), with the ability to negotiate and present effectively in multicultural settings.
• Strong leadership, problem-solving, and decision-making skills in complex, matrixed environments.
• High adaptability to diverse business cultures and flexibility for frequent international travel.

4. Education:

• Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemical Engineering, Business Administration, or related fields.
• PMP, Lean Six Sigma, or other operational certifications are advantageous.