Automation Solutions Engineer - Pharma GMP

GSK; Rosia; On-site; EUR 38,000 - 63,000; Full time

Job summary

GSK in Rosia, Italy is seeking an Automation and Digital Solution Engineer to drive automation projects across the site, ensuring standardization, compliance, and timely delivery. You will collaborate with cross-functional teams to implement robust automation solutions and maintain detailed design and operation documentation.

Requirements include a Master’s degree in Engineering and at least 3 years in GMP pharmaceutical/biotech environments, with fluent Italian and good English.

Qualifications

• Master’s degree in Engineering (Automation, Electronic, Informatic, Process Engineering).
• Fluent Italian and a good level of English (written and spoken).

Responsibilities

• Drive execution of automation activities in the assigned projects with focus on standardization and robust automation strategy.
• Ensure effective reporting to Automation Solution Manager.
• Participate in developing the Automation Solutions team and resolve performance issues.
• Coordinate installation, configuration, and integration of automation systems with cross-functional teams.
• Deliver automation projects on time, within scope and budget.
• Maintain documentation of automation solutions including design specs and procedures.
• Ensure compliance with regulatory standards and company policies.
• Apply Health, Safety and Environment regulations and escalate risks as needed.

Skills

Fluent Italian

English proficiency

Team player

Active listening

Communication skills

Quality/Compliance/EHS mindset

Prioritization

Integrity under pressure

Problem solving

Project scheduling

Risk awareness

Scope management

Construction management

Data integrity

Design management

Digital fluency

GxP regulations

Lean management

Manufacturing technologies

Pharmaceutical manufacturing

Education

Master’s degree in Engineering

Job description

GSK in Rosia, Italy is seeking an Automation and Digital Solution Engineer to drive automation projects across the site, ensuring standardization, compliance, and timely delivery. You will collaborate with cross-functional teams to implement robust automation solutions and maintain detailed design and operation documentation.

Requirements include a Master’s degree in Engineering and at least 3 years in GMP pharmaceutical/biotech environments, with fluent Italian and good English.