We are currently hiring for a world-class Biomanufacturing facility, where you will drive the end-to-end delivery of complex capital and expense projects across a diverse portfolio. As a key technical lead, you will shape site strategy and transform operations across Utilities, Automation/IT, Manufacturing, Labs, and Process systems.
Key Responsibilities
Lead multiple strategic projects simultaneously across the complete lifecycle from initial concept development, scope definition, and business case creation through to commissioning, qualification, and final closeout.
Develop capital project budgets, track spend, make cash flow projections, and utilize enterprise systems (e.g., SAP) to ensure strict financial control and cost optimization.
Assemble and lead multi-disciplinary, matrixed teams (QA, EHS, Manufacturing, Facilities) while managing third-party vendors, suppliers, and engineering contractors to keep milestones on track.
Ensure project solutions incorporate value engineering and constructability reviews. Develop detailed execution plans and actively mitigate risks to avoid business disruptions during site upgrades.
Drive all project stage deliverables in strict alignment with corporate engineering standards, local safety legislation, Good Engineering Practice (GEP), and cGMP guidelines.
Generate technical specifications for process equipment and instrumentation, collaborate with global procurement teams, and oversee FAT/SAT activities and validation support.
Skills, Attributes & Experience
Bachelor's degree in Chemical, Mechanical, Automation, Process Engineering, or a related discipline.
Minimum 5 years of hands-on Project Management experience delivering capital projects across the full lifecycle within a regulated pharmaceutical or biopharmaceutical manufacturing environment.
Proven ability to manage complex projects spanning process equipment, utilities, automation, and facility upgrades. Strong knowledge of project planning tools, cost control, and SAP.
Exceptional interpersonal and communication skills with a track record of successfully influencing cross-functional teams, managing senior stakeholders, and mentoring intermediate project engineers.
PMP certification, Chartered Engineer (CEng) status, and direct exposure to Biologics manufacturing facilities is highly desirable.
