Project engineer- equipment

Project Engineer Job Description

We are seeking a highly motivated Project Engineer to join our Product Transfer & Tech Transfer team. This role is essential in supporting the PMO responsible for transferring product manufacturing across global sites.

* Lead and deliver engineering projects, ensuring they meet timeline, budget, safety, and quality goals.
* Scope new engineering projects and secure capital approval.
* Lead, support, and participate in commissioning and qualification activities for both current and future projects.
* Provide updates and influence management and key project stakeholders.
* Coordinate specialist trades, departments, and third parties (suppliers, customers, service providers).
* Oversee project interfaces between different teams, projects, and external partners.
* Manage project documentation, ensuring accuracy and compliance.
* Handle cost estimation (tracking, updating, auditing, and forecasting).
* Develop and maintain project schedules (tracking, updating, reviewing, forecasting).
* Report project progress and manage associated risks.
* Conduct constructability, maintainability, and operability studies.
* Manage project resources effectively.
* Amb Assess and ensure system compliance (structural, E&I, safety, permitting, and documentation).
* Conduct retrospective project performance reviews and implement lessons learned.
* Participate in and lead cross-functional teams as required.

* Ensure safe execution of job activities, adhering to environmental and regulatory best practices.
* Perform both routine and non-routine tasks as delegated by the manager.
* Maintain compliance with corporate, cGMP, and EHS regulatory requirements.
* Follow engineering and site procedures, ensuring documentation meets GDP standards.
* Prioritize and schedule tasks to align with business needs.
* Complete personal training in compliance with site procedures.
* Provide support to Operations, Quality Validation, MSAT, Facilities, and other functions.
* Represent the company in external site visits for project-related activities.
* Lead by example and maintain high-performance standards.

* Bachelor's or Masters degree in Engineering, Science or related discipline.
* 3-4 years experience in a similar role within a GMP regulated environment.
* Prior experience working within Medical Devices will be an advantage.
* Strong understanding of validation documentation: IQ, OQ, PQ, FAT, SAT, URS (editing/approving experience required, not creation).
* Ability to analyze data and statistics for project tracking and decision-making.
* Willingness to travel internationally once a month.

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