Site Process Engineer

Experteer Overview In this role you will optimize pharmaceutical manufacturing processes to ensure efficiency, robustness and GMP/regulatory compliance. You will support production, technology transfer and continuous improvement within Global Tech Ops & Supply. You will analyze process data, drive improvements, and ensure compliant documentation and CAPA closure.

This role offers the chance to contribute to end-to-end manufacturing and process validation in a global, quality-driven environment.

Retribuzione / Benefits Manage and optimize pharmaceutical manufacturing processes (drug substance and/or drug product)
Ensure compliance with GMP and regulatory requirements (FDA, EMA, ICH)
Support process validation activities (IQ/OQ/PQ) and ongoing CPVAssist technology transfer from development to manufacturing from an engineering perspective

Monitor process performance using data analysis and implement improvements

Investigate deviations and non-conformances; implement CAPACollaborate with cross-functional teams (Manufacturing, Quality Assurance, Validation, HSE)
Contribute to process risk assessments (FMEA) and control strategies

Support audits and regulatory inspections

Drive and support continuous improvement initiatives

Ensure proper GMP-compliant documentation

Responsabilità8+ years of experience in pharmaceutical manufacturing or process engineering

Strong knowledge of GMP and regulatory frameworks (FDA, EMA)

Experience with process validation and manufacturing support

Good understanding of data analysis and process monitoring tools

Strong problem-solving and organizational skills

Strong knowledge in automation applied to pharmaceutical process

Requisiti fondamentalicomprehensive healthcare programswork-life balance initiativesrelocation supportcompetitive salary with performance bonusesflexible working arrangementsremote work options
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