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Major Accountabilities:
- Manage end-to-end project lifecycle: design, business case preparation, approval, execution, qualification/commissioning, and hand-over.
- Prepare and control project budgets, cost estimations, and schedules.
- Develop procurement plans, lead tendering and vendor selection processes.
- Ensure compliance with HSE, GMP, and regulatory requirements throughout project execution.
- Coordinate with cross-functional teams and global/local stakeholders.
- Develop and support cost saving and productivity improvement projects
- Maintain accurate project documentation and reporting.
- Follow and introduce technological developments especially Pharmaceutical Equipment Technology and Automation
- Provide technical support to all Engineering activities and other business units to improve processes when required
- Support internal and external audits related to projects.
- On-time and on-budget project delivery.
- Compliance with safety and quality standards (zero critical findings, no LTI/SIF).
- Reliability and operability of implemented solutions.
- Continuous improvement in cost efficiency and sustainability.
Minimum Requirements
- Bachelor’s degree in Engineering (Mechanical, Electrical or Mechatronics)
- Minimum 5 years in project management within pharmaceutical or manufacturing environment.
- Proven track record in managing CAPEX projects and cross-functional teams.
- Project Management (PM tools, scheduling, risk management).
- Knowledge of GMP, HSE regulations, and compliance standards.
- Strong analytical and problem-solving skills.
- Excellent communication and stakeholder management.
- Fluent in English (written and spoken).
- Familiarity with automation systems and utilities.
- Experience with continuous improvement methodologies (Lean, Six Sigma).
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