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Perrigo Company plc
Perrigo Company plc
5 001 – 10 000 Darbuotojai
GamybaMaistas ir gėrimaiSveikatos priežiūra
„Perrigo Company plc“ kuria ir gamina vartotojų sveikatos priežiūros produktus, skirtus kasdienei sveikatai ir gerovei palaikyti. Įmonės asortimentą sudaro nereceptiniai vaistai, maisto papildai ir asmens higienos priemonės, o jos veiklą formuoja sveikatos priežiūros, gamybos ir į vartotojus orientuotos kompetencijos. Įmonė suburia pardavimų, rinkodaros, mokslinių reikalų ir kitų sričių komandas, kad prieinami sveikatos priežiūros sprendimai pasiektų platų vartotojų ratą.
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Darbai įmonėje

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.

USJungtinės ValstijosNYNiujorkas
95 000 $ – 120 000 $ / metai
Darbas vietojeVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųInžinierius

Aprašymas

  • 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.

Reikalavimai

  • 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.

Privalumai

  • 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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NuotolinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųRezultatais grindžiama rinkodara

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HUVengrija
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NuotolinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųPartnerių rinkodaraPartnerių rinkodaros vadovas

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