Perrigo Company plc
Perrigo Company plc
Perrigo Company plc izstrādā un ražo patēriņa veselības aprūpes produktus, kas paredzēti ikdienas veselības un labklājības atbalstam. Uzņēmuma produktu klāstā ietilpst bezrecepšu zāles, uztura bagātinātāji un personīgās higiēnas produkti, bet tā darbību veido veselības aprūpes, ražošanas un uz patērētājiem vērsta kompetence. Uzņēmums apvieno pārdošanas, mārketinga, zinātnisko jautājumu un citu jomu komandas, lai padarītu pieejamus veselības aprūpes risinājumus plašam patērētāju lokam.

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.

Apraksts

  • 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.

Prasības

  • 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.

Priekšrocības

  • 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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