8 дней назад
Head of Engineering & Projects (Modulus)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Head of Engineering & Projects (Modulus) (Biopharmaceutical Engineering and Capital Projects): Leading Tier 3 capital projects and process engineering support for modular multi-product biopharmaceutical manufacturing facilities with an accent on project execution, automation controls, commissioning, and GxP compliance. Focus on evaluating and prioritizing site investments, managing design-to-qualification workstreams, troubleshooting complex equipment and process issues, and developing engineering teams.
Location: City of Singapore; onsite engineering and manufacturing role
Company
is developing the Modulus program to create modular, adaptable, multi-product manufacturing facilities for vaccines and Specialty Care Biologics.
What you will do
- Lead Tier 3 capital projects valued below €5 million, including feasibility, funding, execution, design, procurement, construction, and commissioning and qualification.
- Drive site capital expenditure committees and prioritize project and process improvement initiatives.
- Manage process engineering support for manufacturing and contribute to site master planning and strategy.
- Coordinate project work packages, contracts, spending phases, progress tracking, and integration of global Engineering projects into site operations.
- Ensure engineering activities, contractors, and suppliers meet HSE, quality, GMP, FDA, and other applicable regulatory standards.
- Lead and develop Site Tier 3 Project Leads, C&Q specialists, Process Engineers, and Plant Engineers.
Requirements
- Degree or Master’s degree in Chemical, Mechanical, Electrical, or Industrial and Systems Engineering.
- At least 10 years of cumulative experience across project management, commissioning and qualification, and process engineering in biopharmaceutical or API manufacturing; experience in all three areas is required.
- Prior GxP experience and a track record of equipment and process troubleshooting and commissioning are required.
- Hands-on experience with process engineering, equipment design, instrument connectivity, and DeltaV automation systems is advantageous.
- Strong knowledge of pharmaceutical regulations, GMP, FDA standards, quality, safety, and local statutory requirements.
- Strong people management, analytical, problem-solving, and cross-functional collaboration skills.
Culture & Benefits
- Work within a global manufacturing and supply organization focused on advancing vaccine and biologics production.
- Collaborate with global subject-matter experts through a community of practice to improve standards, best practices, and lessons learned.
- Build and develop a high-performing engineering and projects team.
- promotes equal opportunity and an inclusive workplace.
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