̽»¨ºÏ¼¯

̽»¨ºÏ¼¯ is seeking a dedicated individual for the role of Maintenance Engineer. The successful candidate will be responsible for overseeing GMP and non-GMP utilities and equipment engineering. This includes managing external vendors and contractors, ensuring maintenance and calibration activities are performed, documented, reviewed and approved in the computerised maintenance management system (CMMS). The role also involves providing routine engineering support for utilities and laboratory equipment, as well as project engineering and validation support.

Responsibilities:

• Oversee utilities, facility owned equipment and systems, including troubleshooting equipment to determine root cause of failure modes, owning corrective and preventative actions and associated change controls.
• Collaborate with cross-functional teams and/or lead investigations into equipment issues, including technical writing of required quality documentation.
• Oversee outside vendors and contractors to ensure work is performed and documented in compliance with cGMP policies and procedures.
• Review and approve vendor documentation for accuracy and compliance in the CMMS system.
• Ensure all work is performed in accordance with Standard Operating Procedures (SOPs), Current Good Manufacturing Practices (cGMP), safety procedures, quality standards, EH&S guidelines, and good maintenance practices.
• Promote safety within the workplace by following site safety procedures, ensuring contractors are following safety requirements, performing proactive safety assessments, and fostering a safe work culture.

Key Skills and Requirements:

• BSC equivalent minimum requirement in a related field.
• Proven history within the biotech pharmaceutical environment is preferred.
• Deep knowledge of Microsoft Office
• Familiarity with Computerised Maintenance Management System (CMMS) to record maintenance work activities.
• Knowledge of cGMP documentation - Facilities documentation (work orders, equipment files, calibrations, developing SOPs) and QA systems (CAPAs, deviations, change controls).
• Knowledge of equipment Qualification and Validation requirements.
• Excellent communication and interpersonal skills, attention to detail, flexibility and technical writing skills.
• Ability to work independently or in a team environment, self-motivated and showing initiative.

If you are having difficulty in applying or if you have any questions, please contact Ruhee Saleh on r.saleh@proclinical.com.

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

̽»¨ºÏ¼¯ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ̽»¨ºÏ¼¯ is acting as an Employment Agency in relation to this vacancy.