Perrigo Company plc
Perrigo Company plc
5,001 – 10,000 Employees
Food & BeverageHealthcareManufacturing
Perrigo Company plc develops and produces consumer healthcare products designed to support everyday health and well-being. Its portfolio spans over-the-counter medicines, dietary supplements, and personal care products, with work shaped by healthcare, manufacturing, and consumer-focused expertise. The company brings together teams across areas such as sales, marketing, and scientific affairs to make accessible healthcare solutions available to a broad range of consumers.

Process Engineer, Pharmaceutical Manufacturing

Support and improve Perrigo’s prescription, over-the-counter, and topical product manufacturing processes. The role covers scale-up, technology transfer, investigations, validation, and regulatory documentation.

Description

  • Provide technical support for commercial prescription, over-the-counter, and topical cosmetic products.
  • Assess processes and provide ongoing support to maintain quality, efficiency, and compliance.
  • Direct technology transfers into commercial operations.
  • Develop, improve, and implement manufacturing processes.
  • Investigate production issues, process deviations, and product failures.
  • Analyze root causes and recommend corrective and preventive measures.
  • Maintain and update manufacturing and related regulatory records.
  • Conduct formulation and process development studies at laboratory scale.
  • Review process performance data to find improvement and cost-saving opportunities.
  • Contribute to Material Review Board activities.
  • Take part in process excellence, performance qualification, continued verification and validation, and other validation work.
  • Work with Regulatory Affairs, Quality Assurance, Research and Development, Operations, and Legal teams.
  • Prepare technical reports, protocols, investigation records, and supporting documents for process changes, validation, and regulatory submissions.
  • Oversee multiple projects and meet agreed timelines and business goals.

Requirements

  • Bachelor’s degree in pharmaceutical sciences, chemical engineering, pharmaceutical engineering, chemistry, or a related scientific field.
  • Two to five years of experience in pharmaceutical manufacturing, process engineering, technical services, or process support in a regulated setting.
  • Strong grasp of pharmaceutical manufacturing, pharmaceutical sciences, and process engineering principles.
  • Knowledge of cGMP requirements, FDA regulations, and pharmaceutical quality systems.
  • Strong interpersonal, organizational, and communication abilities.
  • Skilled in technical writing, documentation, and problem solving.
  • Able to independently manage several projects and priorities while meeting deadlines.
  • Practical experience using laboratory-scale manufacturing equipment.
  • Familiarity with commercial-scale pharmaceutical processing equipment.
  • Proficient with Microsoft Office, including Excel, Word, PowerPoint, and OneNote.
  • Submit all application materials, including a resume or CV, in English.

Benefits

  • Competitive compensation.
  • Benefits designed to support employees and their families.
  • Career development opportunities.
  • Inclusive and collaborative workplace culture.
  • Equal opportunity employment.

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