GMP Mechanical Engineer - Pharma Manufacturing

ARTO; Maidstone; On-site; GBP 42,000 - 55,000; Full time

Job summary

ARTO in a GMP-regulated pharmaceutical manufacturing environment is seeking a Mechanical Engineer to support equipment and site infrastructure. The role focuses on troubleshooting, maintenance, and engineering documentation to uphold GMP standards.

Candidates should have a mechanical engineering background and experience in pharmaceutical or GMP-regulated settings, with strong hands-on problem-solving abilities and ability to read technical drawings.

Qualifications

• Must have a mechanical engineering background.
• Experience in pharmaceutical/ GMP environments is required.
• Hands-on mechanical troubleshooting and repair experience.

Responsibilities

• Support mechanical engineering activities across manufacturing equipment and site infrastructure.
• Troubleshoot and resolve mechanical issues affecting operations.
• Assist with preventive and corrective maintenance.
• Contribute to equipment upgrades and project improvements.
• Collaborate with Engineering, Maintenance, Production and Quality teams.
• Support installation, commissioning and qualification of new or modified equipment.
• Ensure activities align with GMP requirements and site procedures.
• Maintain accurate engineering and technical documentation.

Skills

Mechanical troubleshooting

Equipment experience

Reading drawings

Problem solving

Education

Mechanical Engineering degree

Job description

ARTO in a GMP-regulated pharmaceutical manufacturing environment is seeking a Mechanical Engineer to support equipment and site infrastructure. The role focuses on troubleshooting, maintenance, and engineering documentation to uphold GMP standards.

Candidates should have a mechanical engineering background and experience in pharmaceutical or GMP-regulated settings, with strong hands-on problem-solving abilities and ability to read technical drawings.