- 経験
- 10年以上
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 3時間前
- 作業モード
- 在任中
- 教育
- Degree or Master's in Engineering (Chemical / Mechanical / Electrical / Industrial & Systems)
- 再開する
- 応募必須
勤務地
仕事内容
About The Role
Sanofi's Manufacturing and Supply division is embarking on the Modulus initiative, a pivotal program designed to revolutionize manufacturing by introducing adaptable, modular, and multi-product facilities. These next-generation plants will incorporate cutting-edge technologies to meet the evolving demands of vaccine production and Specialty Care Biologics.
Key Accountabilities
- Oversee Tier 3 capital expenditure projects (under 5 million euros) at the facility.
- Lead site Capex committees by managing the evaluation, prioritization, and funding decisions for projects and process enhancements.
- Conduct feasibility assessments and provide technical input for early project stages to aid site and central leadership decision-making.
- Deliver process engineering support to manufacturing teams as required.
- Contribute to site master planning and strategic development initiatives.
- Manage execution of project work packages encompassing contract oversight, phased expenditure, and progress monitoring.
- Take ownership of Tier 3 projects from design through procurement, construction, and commissioning & qualification phases.
- Advise on engineering strategies ensuring compliance with industry regulations and standards.
- Collaborate with global subject matter experts to refine standards, best practices, and lessons learned.
- Implement initiatives to boost efficiency, safety, and quality within engineering and maintenance departments.
- Oversee selection and performance of external contractors and suppliers, ensuring adherence to HSE and quality standards.
- Lead workforce planning and staffing of site engineering and project teams from design through qualification phases.
- Coordinate integration of Tier 1 and Tier 2 (Global Engineering) projects into site operations, including post-qualification support and handover.
- Direct and mentor a team of engineering professionals including Tier 3 project leads, commissioning and qualification experts, and process and plant engineers.
Candidate Profile
- Holds an engineering degree or master's in Chemical, Mechanical, Electrical, or Industrial & Systems Engineering.
- Possesses at least 10 years of combined experience in Project Management, Commissioning & Qualification (C&Q), and Process Engineering within biopharmaceutical or API manufacturing sectors; proficiency across all three areas is mandatory.
- Demonstrated success in planning, executing, and monitoring large-scale projects.
- Hands-on knowledge of DeltaV automation systems, instrumentation connectivity, and equipment design, with capacity to engage technically as needed.
- Proven practical engineering skills including direct involvement in troubleshooting complex issues alongside operational engineers.
- Strong analytical and problem-solving abilities for resolving technical challenges.
- Well-versed in regulatory requirements including GMP, FDA, and local statutory standards relevant to pharmaceuticals.
- Dedicated to quality and safety ensuring full compliance throughout all project phases.
- Effective leadership and people management skills with experience collaborating across multifunctional teams.