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Perrigo Company plc

Process Engineer

Perrigo Company plc

. Provide technical and scientific support for commercial prescription, over-the-counter, and cosmetic topical products .

Posted 10/13/2026full-timeBronx • New York • United StatesJuniorMid-Level💰 $95,000 - $120,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in pharmaceutical manufacturing processes, technical assessments, and compliance with cGMP and FDA regulations. Capable of managing multiple projects while ensuring quality and efficiency in process development and validation.

Highest-signal resume keywords
Pharmaceutical Manufacturing ProcessesCGMP RequirementsTechnical WritingProcess Engineering PrinciplesLaboratory-Scale Manufacturing Equipment

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Process DevelopmentRoot Cause AnalysisProcess ImprovementTechnical AssessmentsRegulatory DocumentationManufacturing Process OptimizationQuality SystemsProcess Performance QualificationValidation ActivitiesProject Management
Soft Skills
Interpersonal SkillsOrganizational SkillsCommunication SkillsProblem-Solving Skills
Tools & Technologies
Microsoft OfficeExcelWordPowerPointOneNote
Industry Keywords
Pharmaceutical SciencesChemical EngineeringRegulated EnvironmentTechnical ServicesProcess SupportCommercial OperationsMaterial Review BoardProcess VerificationProcess ValidationProduct Failures

About the role

Key responsibilities & impact
  • Provide technical and scientific support for commercial prescription, over-the-counter, and cosmetic topical products
  • Conduct technical assessments and ongoing process support to ensure quality, efficiency, and compliance
  • Lead technology transfer activities into commercial operations
  • Develop, optimize, and implement manufacturing processes
  • Investigate manufacturing issues, process deviations, and product failures
  • Perform root cause analyses and recommend corrective and preventive actions
  • Review, revise, and maintain manufacturing and associated regulatory documentation
  • Perform laboratory-scale formulation and process development studies
  • Evaluate process performance data and identify process improvement and cost-reduction opportunities
  • Support Material Review Board activities
  • Participate in process excellence, process performance qualification, continued process verification/validation, and other validation activities
  • Collaborate with Regulatory Affairs, Quality Assurance, Research & Development, Operations, and Legal teams
  • Prepare technical reports, protocols, investigations, and documentation for process changes, validation, and regulatory submissions
  • Manage multiple projects while meeting timelines and business objectives

Requirements

What you’ll need
  • Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutical Engineering, Chemistry, or a related scientific discipline
  • 2–5 years of pharmaceutical manufacturing, process engineering, technical services, or process support experience in a regulated environment
  • Strong understanding of pharmaceutical manufacturing processes, pharmaceutical sciences, and process engineering principles
  • Knowledge of cGMP requirements, FDA regulations, and pharmaceutical quality systems
  • Excellent interpersonal, organizational, and communication skills
  • Strong technical writing, documentation, and problem-solving skills
  • Ability to independently manage multiple projects and priorities while meeting established timelines
  • Hands-on experience with laboratory-scale manufacturing equipment
  • Understanding of commercial-scale pharmaceutical processing equipment
  • Proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, and OneNote
  • All application materials, including resumes and CVs, must be submitted in English

Benefits

Comp & perks
  • Competitive compensation
  • Benefits tailored to supporting you and your family
  • Career development opportunities
  • Inclusive, collaborative culture
  • Equal opportunity employment