Head of Engineering & Projects

* Provide input and studies to support decision making process with site leadership team and central function.
* Deciding on the initiation and funding of capital projects.
* Capital Project delivery model (workforce, study, execution plan, contracts with 3rd party...) for design to closure.
* Advising on strategies to ensure all engineering activities comply with industry regulations and standards.
* Implementing process improvements to enhance efficiency, safety, and quality within the engineering and maintenance groups.
* Selection and management of external contractors and suppliers to ensure they meet the company's standards and requirements.
* Staffing of site Engineering and Project teams based on site needs and strategic workforce planning.
* Performs strategic planning and development activities for site CQ, including compliance, capacity, timeline and direction.
* Align department objectives with Engineering and site business objectives.
* Collaborate with senior leadership in meeting organizational goals.
* Establish and report applicable department or organizational metrics.
* Direct the development of projects and conduct follow-up and reporting.
* Interact with project teams and cross functional groups.
* Represent department during internal and external audits and inspections
* Interface with external regulatory agencies as required.
* Ensure and maintain harmonized approaches across CQV teams
* OpEx Scope of Responsibility:
Team size, maintenance budget and energy & utilities budget
* CAPEX Scope of Responsibility:
Routine MCP budget and 5-8 yrs look ahead with site master plan
* Complexity of Role:
Technical expertise required, regulatory environment and project portfolio
* Impact on Business Outcomes of M&S
* Size of the site (Large/Medium)
* Project Management:
Proficiency in planning, executing and monitoring large scale projects
* Technical Expertise:
In-depth knowledge of engineering & maintenance principles on pharmaceutical manufacturing processes
* Regulatory Knowledge:
Familiarity with pharmaceutical industry regulations, including GMP and FDA standards
* Problem-solving:
Excellent analytical and problem-solving skills to address technical issues
* Bachelor's degree in Engineering or Science and 12+ years of CQV or relevant experience, or
* Master’s degree in Engineering or Science and 10+ years of CQV or relevant experience
* 5 years of management/supervisory experience highly preferred
* Bring the miracles of science to life alongside a supportive, future-focused team.
* Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
* Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
* Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
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