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Project Engineer

Contract
contract
5 Nov 2025
Dublin South
Verified by Turrior

Content + Source + Freshness • 16 Dec 2025 • 95% confidence

85 / 100

Offer value

Strong potential for professional growth within a dynamic sector, especially for those familiar with pharmaceutical environments.

  • Competitive salary based on pharmaceutical industry standards
  • Scope for career advancement in a growing sector
  • Diverse responsibilities and project phases engagement
  • Requires solid experience in pharmaceutical environments
Pros
  • High demand for skills in pharmaceutical project delivery.
  • Opportunities to work on cutting-edge projects.
  • Exposure to a diverse range of stakeholders and teams.
Cons
  • Requires in-depth knowledge of highly regulated environments.
  • Possible need for frequent travel.
  • Managing cross-functional teams may involve complex dynamics.

Who it's for

Mid to Senior-level • Onsite with travel required

Good fit
  • Project Engineers with a background in pharmaceuticals
  • Candidates who thrive in dynamic project environments
  • Individuals interested in working on innovative drug manufacturing processes
Not recommended for
  • New graduates or those without relevant project engineering experience
  • Candidates seeking static work environments
  • Individuals unprepared for regulatory complexities

Motivation fit

Desire to impact pharmaceutical innovations.Interest in diverse engineering challenges.Willingness to engage with various project phases.

Key skills

Project delivery in a regulated environment.Technical leadership and design documentation.Vendor management and stakeholder influence.
Score: 85/100 AI verified analysis

About the job

We are seeking an experienced Project Engineer with a strong background in pharmaceutical design and project delivery to join the client-side engineering team supporting a fast-track Fill/Finish facility expansion in South Dublin.

This role is part of a high-performing project delivery team responsible for the design, coordination, and implementation of new formulation and component preparation systems as part of a large-scale drug product facility build. The position is ideal for a technically strong engineer with a background in design execution, vendor management, and project delivery within a highly regulated environment.

Key Responsibilities

  • Act as a client-side design engineer, supporting the delivery of formulation and component preparation systems within a large-scale Fill/Finish facility.
  • Provide technical leadership and design input across all project phases - Basis of Design, Detailed Design, Commissioning, and Qualification.
  • Coordinate and integrate design activities between internal engineering teams, design partners, and process equipment vendors.
  • Participate in vendor selection, technical reviews, and FAT/SAT activities, ensuring systems meet technical and quality standards.
  • Offer direction and guidance to cross-functional teams on design execution, schedule, and cost management to achieve project milestones.
  • Review and approve design documentation including URS, SDS, equipment specifications, and design reports.
  • Support automation, commissioning, and validation teams with technical input related to equipment and system design.
  • Provide oversight during construction and installation, ensuring design intent is maintained and delivered.
  • Collaborate with site functions including Maintenance, Calibration, and Metrology to ensure seamless system integration and lifecycle management.

Qualifications & Experience

  • Minimum 5 years' experience in pharmaceutical or biopharmaceutical project engineering, ideally with exposure to both design and project delivery phases.
  • Strong understanding of process equipment, formulation systems, or clean utility design (direct formulation experience advantageous but not essential).
  • Proven ability to manage vendors and third-party partners in a large-scale capital project environment.
  • Experience supporting commissioning, qualification, and validation (CQV) activities.
  • Excellent communication and stakeholder management skills, with the ability to influence and guide multidisciplinary teams.
  • Degree in Chemical, Mechanical, or Process Engineering, or equivalent technical discipline.
  • Previous experience working in a highly regulated cGMP environment.
  • Flexibility to travel for vendor FATs (EU/US) as required.

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