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PCI Pharma Services

Pharmaceutical packaging and contract services

Associate Director - Engineering

Engineering LeadershipConfirmed live in the last 24 hours
Full-timeStamullin, Stamullen, Co. Meath, IrelandNo salary listedIn-person

About the Job

Requirements

  • A degree in an Engineering discipline is required.
  • At least 10 years of experience in the pharmaceutical, medical device, or another regulated industry is required.
  • At least 5 years of leadership experience is required.
  • Strong knowledge of Good Manufacturing Practice, validation, quality systems, and project management is required.
  • Experience managing engineering budgets and capital projects is required.
  • Strong communication and stakeholder management skills are required.
  • Demonstrated experience troubleshooting complex process and equipment issues is required.
  • Experience with automation in an engineering environment is required.
  • Experience supporting equipment qualification, validation, Factory Acceptance Testing, Site Acceptance Testing, and commissioning is required.
  • Understanding of serialization systems and associated regulatory requirements is required.
  • Strong knowledge of current Good Manufacturing Practice, quality systems, risk management, and Good Engineering Practice is required.
  • Experience with structured problem-solving methodologies such as Define, Measure, Analyze, Improve, Control; 5 Why; Fishbone Analysis; or Root Cause Analysis is required.
  • Ability to manage multiple priorities in a fast-paced operational environment is required.
  • Excellent communication, stakeholder management, and presentation skills are required.
  • Strong analytical capability and a data-driven approach to decision-making are required.
  • Proficiency in Microsoft Office, Microsoft Project, AutoCAD, Visio, and computerized maintenance management systems is required.
  • Strategic leadership, engineering excellence, financial management, compliance, project management, change leadership, innovation, accountability, technical excellence, problem solving and analytical thinking, continuous improvement, leadership through influence, customer focus, collaboration and teamwork, ownership, adaptability, communication, stakeholder management, and integrity are listed as key competencies.

Responsibilities

  • Lead engineering, maintenance, automation, and facilities teams.
  • Develop an engineering strategy aligned with site objectives.
  • Act as the technical subject-matter expert for assigned manufacturing, packaging, serialization, or automation processes.
  • Develop, maintain, and continually improve process knowledge, standards, and best practices across site operations.
  • Provide technical leadership and coaching to operations, maintenance, quality, and engineering teams.
  • Support investigations, root cause analysis, and implementation of effective corrective and preventive actions for process- and equipment-related deviations.
  • Lead initiatives to improve overall equipment effectiveness, throughput, quality performance, reliability, and waste reduction.
  • Apply Lean Manufacturing, Six Sigma, and continuous improvement methodologies to optimize operational performance.
  • Use process data and performance metrics to identify trends, prioritize improvement opportunities, and deliver sustainable solutions.
  • Support Right First Time and On Time In Full performance objectives.
  • Provide advanced troubleshooting support for manufacturing and packaging equipment to minimize downtime.
  • Partner with Maintenance and Operations teams to improve equipment availability, reliability, and maintainability.
  • Identify recurring equipment issues and implement long-term corrective actions.
  • Support predictive and preventive maintenance strategies to maximize asset lifecycle performance.
  • Support automation initiatives involving programmable logic controllers, human-machine interfaces, vision systems, serialization platforms, and digital manufacturing technologies.
  • Collaborate with equipment vendors, original equipment manufacturers, and system integrators to optimize machine functionality and performance.
  • Identify opportunities for digitalization, Industry 4.0 technologies, and process automation to improve productivity.
  • Participate in software modifications, equipment upgrades, and control system improvements where appropriate.
  • Lead or support capital investment planning, User Requirement Specifications, Factory Acceptance Testing, Site Acceptance Testing, commissioning, and qualification execution.
  • Support automation and digital transformation.
  • Prepare business cases and technical justifications for capital investment opportunities.
  • Participate in User Requirement Specification development, equipment selection, procurement, Factory Acceptance Testing, Site Acceptance Testing, installation, commissioning, and validation activities.
  • Ensure projects are delivered safely, on time, within scope, and within budget.
  • Ensure compliance with current Good Manufacturing Practice, Good Distribution Practice, regulatory requirements, company procedures, and Good Engineering Practice.
  • Generate and review engineering documentation, including standard operating procedures, change controls, risk assessments, technical reports, validation documentation, and engineering standards.
  • Maintain technical drawings, equipment specifications, and engineering documentation throughout their lifecycle.
  • Support internal, customer, and regulatory audits as required.
  • Lead and participate in risk assessments, including Failure Mode and Effects Analysis, Hazard and Operability Analysis, machine safety, and process risk evaluations.
  • Ensure engineering risks are identified, assessed, controlled, and documented.
  • Support business continuity and risk mitigation initiatives.
  • Champion a strong safety culture and ensure safe systems of work are followed.
  • Participate in environmental, health, and safety initiatives, risk assessments, incident investigations, and corrective action implementation.
  • Identify opportunities to improve environmental sustainability, energy efficiency, and waste reduction.
  • Ensure safe work practices are followed and report near misses immediately to the Environmental, Health and Safety Department.
  • Collaborate with suppliers, contractors, original equipment manufacturers, and service providers to deliver engineering solutions.
  • Support supplier assessment, qualification, and performance management activities.
  • Build relationships across Operations, Quality, Validation, Supply Chain, Procurement, clients, and customer-facing functions.
  • Monitor emerging technologies, pharmaceutical industry trends, and best practices.
  • Identify strategic opportunities to enhance site capabilities and competitive advantage.
  • Support development of engineering standards, workflows, and operational excellence programs.
  • Lead and participate in continuous improvement projects aligned with site strategic objectives.

Desired Qualifications

  • Multi-site pharmaceutical experience is desirable.
  • Experience with Lean Manufacturing, Six Sigma, Total Productive Maintenance, or Operational Excellence methodologies is desirable.
  • A Green Belt or equivalent Continuous Improvement certification is desirable.
  • Knowledge of machine safety standards and CE compliance is desirable.
  • Experience managing capital projects in a pharmaceutical environment is desirable.

About the Company

PCI Pharma Services

Pharmaceutical packaging and contract services

PCI Pharma Services provides end-to-end pharmaceutical packaging and related services, including folding cartons, labels, contract packaging, clinical services, and brand protection, acting as a one-stop source for healthcare product development and commercialization. It handles packaging operations from cartons and labels to contract packaging and labeling, plus clinical packaging and brand protection, with processes built on cGMP and ISO compliance, lean manufacturing, and ongoing R&D, supported by mandatory training and strict security, hygiene, and inspections. It differentiates itself with eight decades of experience and a broad, integrated service suite under one roof, reducing risk and handoffs for clients. Its goal is to be a trusted packaging partner that delivers reliable, compliant, and scalable solutions so healthcare brands stay protected and clients can focus on their core business.

Company size
1-10
Company stage
Debt Financing
Total funding
$4B
Headquarters
Burlington, Canada
Founded
1971

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