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Project Engineer R&DConfidential • Dublin, Dublin, Ireland
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Confidential

Project Engineer R&D

Confidential
  • IE
    Dublin, Dublin, Ireland
  • IE
    Dublin, Dublin, Ireland
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À propos

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe.
Scroll down to find an indepth overview of this job, and what is expected of candidates Make an application by clicking on the Apply button.
Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work.
Here our employees can fulfill their life's purpose through the work that they do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.
Our Total Rewards program
- which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components
- is designed to support the varying needs of our diverse and global employees.
The Project Engineer leads cross functional projects that support embecta' s injection products portfolio.
This role plays a key part in delivering projects that ensure regulatory compliance, support product changes, and enable business continuity and growth.
The position offers the opportunity to manage initiatives that are critical to the long term success of the business.
About the Role Lead cross functional project teams delivering initiatives that impact compliance, form/fit/function, cost reduction, line extensions, and other business opportunities.
Act as a primary liaison between business leadership, functional management, and project team members.
Collaborate with functional managers to ensure appropriate resource allocation and discretionary spending to meet project timelines.
Plan and facilitate regular project meetings to ensure all stakeholders are informed, aligned, and completing assigned actions.
Work closely with Technical Subject Matter Experts (SMEs) to ensure all project tasks are clearly defined, planned, and executed.
Assess the impact of change requests, including risks, costs, and schedule implications.
Manage, and in some cases execute, engineering change deliverables through all stages of the Change Control process.
Provide regular project status updates to senior management, covering quality, schedule, cost, and overall progress.
Promote strong project planning, execution discipline, and rigor across all project activities to ensure successful outcomes.
What you bring Bachelor's degree in an engineering or technology-related discipline.
Experience working in a regulated Medical Devices and/or Pharmaceutical industry environment Experience with product lifecycle management in high-volume manufacturing environments.
Solid understanding of structured product development processes, regulatory requirements, and quality systems.
Experience with ISO standards, GMP guidelines, FDA regulations, medical device design controls, and manufacturing scale-up processes.
Excellent interpersonal and communication skills, with the ability to efficiently interact with diverse audiences and stakeholders Proven ability to work effectively both independently and as part of a cross-functional team.
Strong attention to detail and commitment to quality and compliance.
#LI-DF1 embecta is an Equal Opportunity/Affirmative Action Employer. xyswxtq
We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
TPBN1_IJ
  • Dublin, Dublin, Ireland

Compétences linguistiques

  • English
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