Company Profile:
CPL are partnered with a multinational biopharmaceutical organization with three sites country-wide and a far-reaching global presence. They are actively seeking a Utilities Engineer specialized in Facilities & Soft services to be based on their best in class Dublin branch. This would be an initial 12-month contract with the opportunity to work closely and learn from experienced industry professionals and gain exposure to a variety of tasks within the biopharma sector.
Job Summary:
The role is part of the Engineering Department working with various site stakeholders and service providers. Overseeing service delivery and maintaining and developing relationships with service providers in partnership with stakeholders such as Operations, Maintenance, EHS, Quality, Procurement and Global Departments.
Ensuring all the operating systems are in compliance with all Regulatory and Legal requirements including, EPA license, Quality (cGDP/GMP’s), EHS, Global Engineering, design & construction directives, requirements & procedures. Support for regulatory and corporate audits.
Core Responsibilities:
• Manage GxP and non-GxP related Service Provider contracts supporting Site Operations.
• Through Service Providers always maintain the facility in a GMP state and audit ready.
• Safety, Quality and non-Quality related investigations associated with service delivery from Service Providers.
• Provide Facilities technical support and oversight to the site projects team
• Budget management and optimization of services delivered
Contracts in scope include:
o Facility management, maintenance and repair across all sites
o Sanitization & cleaning of production areas, labs and support areas as required.
o Pest Control for production areas & non-production Areas.
o Laundry & delivery of garbing for production areas and non-production areas.
o Catering provision in the Restaurant and break areas across the site.
o Security systems including access control & CCTV.
o Lab supplies and lab services support.
Essential Requirements:
• Bachelors (Level 8) Science/Engineering discipline with at least 6 years’ experience providing technical expertise on an operating site.
• Strong leadership, performance management and employee development skills.
• GMP experience and safety knowledge an advantage.
• Strong project management skills i.e. budget tracking, schedule development and adherence, project reporting, etc..
• Familiarity with manufacturing environments would be an advantage.
• Demonstrated communication, administrative and leadership skills with ability to work well with other departments, and effectively and efficiently lead in a team environment.
• Proven ability to manage multiple priorities in a fast-paced environment. Ability to understand, implement, and monitor regulatory and safety guidelines applicable to the pharmaceutical industry.
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