Validation Engineer – Pharma Systems & Equipment (EU GMP)

Chiesi Group; Turbigo; On-site; EUR 40,000 - 65,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive healthcare programs

Work-life balance initiatives

Robust relocation support

Flexible working arrangements

Remote work options

Job summary

A renowned biopharmaceutical company in Italy is seeking a Validation Engineer for its new site in Nerviano. The role involves developing Validation Master Plans and overseeing Commissioning and Qualification activities for pharmaceutical manufacturing, specifically respiratory products. Candidates should have a degree in Engineering or related fields and a minimum of 5 years of relevant experience. Offering competitive salary, flexible work arrangements, and comprehensive benefits.

Qualifications

• Minimum 5 years of experience in pharmaceutical Commissioning and Qualification.
• Solid knowledge of EU GMP and FDA regulations.
• Demonstrated experience in Systems and Equipment Commissioning.

Responsibilities

• Develop Validation Master Plans for Systems and Equipment.
• Support management of Commissioning and Qualification activities.
• Collaborate with cross-functional teams on C&Q activities.

Skills

Commissioning and Qualification

Regulatory Compliance

Communication

Problem-solving

Attention to Detail

Education

Degree in Engineering, Pharmacy, Chemistry, or related

Tools

EU GMP

FDA CFR 21 Part 11

Annex 15

GAMP 5

Job description

A renowned biopharmaceutical company in Italy is seeking a Validation Engineer for its new site in Nerviano. The role involves developing Validation Master Plans and overseeing Commissioning and Qualification activities for pharmaceutical manufacturing, specifically respiratory products. Candidates should have a degree in Engineering or related fields and a minimum of 5 years of relevant experience. Offering competitive salary, flexible work arrangements, and comprehensive benefits.