Site Engineer

ACCPRO; Munster; On-site; EUR 60,000 - 80,000; Full time

Job summary

A leading pharmaceutical company in Kerry is seeking a Validation/Maintenance Engineer responsible for maintaining and calibrating manufacturing equipment. Ideal candidates will have a pharmaceutical background, experience with regulatory audits, and technical writing skills. Applicants should possess a relevant technical qualification. For more information, contact Alan at the provided email.

Qualifications

• Experience ensuring that the PM/Validation Schedule is adhered to.

Responsibilities

• Responsible for the overall maintenance and calibration of all manufacturing equipment.
• Oversee the validation, calibration and maintenance of the Purified Water systems.
• Manage, train and motivate production/maintenance operators.

Skills

Pharmaceutical background

Regulatory audits experience

Technical writing skills

Education

3rd level technical qualification in life sciences or similar

Job description

Overview

Validation/ Maintenance Engineer

Location: Kerry - Onsite

Duration: Full Time Permanent

Industry: Pharmaceutical

Responsibilities

• To be responsible for the overall maintenance and calibration of all manufacturing equipment and instrumentation.
• Responsible for the validation, calibration and maintenance of the Purified Water and WFI systems, the HVAC system and autoclaves.
• Oversee engineering function and ensure PM schedule and Master Validation Plan is adhered to and all associated records updated
• To be responsible for IQ, OQ, PQ for all new and existing equipment.
• To review the Batch Manufacturing Records prior to quality review and final review by the QP in a timely manner.
• To manage, train and motivate production/maintenance operators.
• To monitor, review and improve efficiency and quality.
• Interaction with Production/QA & QC departments.
• Assist with the purchasing and replacing equipment while maintaining high maintenance standards of equipment.
• Maintaining and agreeing service contracts with service providers.

Qualifications

• Pharmaceutical background
• Experience with regulatory audits
• Experience ensuring that the PM/Validation Schedule is adhered to
• Technical writing of paperwork associated with PM/Validations and report writing.
• 3rd level technical qualification in life sciences or similar.

How to apply

For more information, please contact Alan on [e-mail] or click apply now