Pharma Process Engineer — Remote & Process Optimization

Biopharma Careers; Parma; Ibrido; EUR 36.000 - 44.000; Tempo pieno

Vantaggi offerti da questo lavoro

Pension

Private medical insurance

Wellbeing programme

Flexible benefits programme

Relocation support

Descrizione del lavoro

Chiesi is seeking a skilled Process Engineer to oversee and optimize pharmaceutical manufacturing processes at our Parma site. The role focuses on ensuring process efficiency, robustness, and GMP/regulatory compliance while supporting production, tech transfer, and continuous improvement.

You will manage and optimize processes, support validation activities, collaborate with Manufacturing, Quality Assurance, and Validation teams, and contribute to risk assessments and continuous improvement

Competenze

• Experience in manufacturing or process engineering is required.
• Knowledge of GMP and regulatory requirements is preferred.
• Familiarity with data analysis and process monitoring tools is beneficial.

Mansioni

• Manage and optimize pharmaceutical manufacturing processes (drug substance and/or drug product).
• Support process validation activities (IQ/OQ/PQ) and ongoing process verification (CPV).
• Collaborate with cross-functional teams including Manufacturing, Quality Assurance, Validation, and HSE.
• Contribute to process risk assessments (FMEA) and control strategies.
• Drive continuous improvement initiatives and ensure GMP documentation.

Conoscenze

Process optimization

Data analysis

Regulatory compliance

Cross-functional collaboration

Documentation

Formazione

Bachelor’s or master’s degree in chemical engineering

Strumenti

MES

SAP

LIMS

Descrizione del lavoro

Chiesi is seeking a skilled Process Engineer to oversee and optimize pharmaceutical manufacturing processes at our Parma site. The role focuses on ensuring process efficiency, robustness, and GMP/regulatory compliance while supporting production, tech transfer, and continuous improvement.

You will manage and optimize processes, support validation activities, collaborate with Manufacturing, Quality Assurance, and Validation teams, and contribute to risk assessments and continuous improvement