GerTEK Project Management & Technical Services is an outsourced technical services provider delivering worldwide contract and permanent staffing solutions. We are accepting applications for our Equipment Validation Engineer role based in Sligo.
Summary:
Ensures optimal performance and reliability of pharmaceutical manufacturing equipment through proactive maintenance strategies, engineering solutions, and GMP compliance.
Responsibilities:
* Develop and implement preventative maintenance programs.
* Troubleshoot complex equipment issues and provide engineering solutions.
* Lead equipment qualification (IQ/OQ/PQ) and validation activities.
* Manage equipment documentation and maintenance records within CMMS.
* Drive continuous improvement initiatives for equipment performance and reliability.
* Ensure compliance with GMP, safety, and regulatory standards.
* Manage vendor relationships for equipment maintenance and repairs.
Qualifications:
* Bachelor's degree in Engineering (Mechanical, Electrical, or related).
* Experience in pharmaceutical manufacturing maintenance engineering or similar industry.
* Strong knowledge of GMP and regulatory requirements.
* Proficiency in CMMS and data analysis.
* Proven ability to lead equipment qualification and validation.
* Excellent problem-solving and communication skills.
Experience:
* Equipment qualification (IQ/OQ/PQ): 4 years (required)
Work authorization: Ireland (required)
Job Type: Full-time
Seniority level
* Mid-Senior level
Employment type
* Full-time
Job function
* Validation Engineering
Industries
* Pharmaceutical Manufacturing and Medical Equipment Manufacturing
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