We are seeking an experienced automation engineer to join a growing automation project within a pharmaceutical manufacturing environment.
This role requires strong hands-on experience and a deep understanding of GMP-regulated automation projects, ensuring compliance, quality, and on-time delivery.
Key Responsibilities
Ensure full lifecycle deliverables are met in a GMP pharmaceutical facility.
Ensure all project activities comply with GMP, GAMP 5, and pharmaceutical quality standards.
Collaboration between automation, engineering, validation, quality, and business stakeholders.
Drive effective communication and alignment between onsite and offshore teams.
Support CSV/automation validation activities in line with pharma requirements.
Ensure documentation, change control, and audit readiness throughout the project lifecycle.
Required Experience & Qualifications
Minimum 5 years' experience in automation within the pharmaceutical industry or regulated manufacturing.
Proven delivery of
DeltaV
projects in GMP-compliant environments.
Experience with PLC Systems is desirable.
Strong understanding of GMP, GAMP 5, CSV, and FDA/EU regulatory expectations.
Excellent communication skills and ability to work in a team.
12-month initial contract with potential for extension.
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