Healthcare Sernior Facilities Engineer

What are we looking for in our Sernior Facilities Engineer?

Exciting Career Opportunity for a leading pharmaceutical company!!
Senior Engineer, Facilities & Soft Services - 12 months contract - Dublin 15 - €340.00 Daily (LTD)

Russell Tobin is thrilled to partner with a prominent global biologics manufacturer dedicated to elevating patient and staff well-being. Recognized as one of Ireland's premier workplaces, they are committed to driving meaningful change in the biotech landscape.

Our client is seeking to recruit a Senior Engineer for Facilities & Soft Services who will work as part of the Engineering team to deliver services across the site ensuring the site is complying with all necessary Regulatory & Corporate Requirements.

The role is part of the Engineering Department working with various Site Stakeholders and Service Providers.

The Engineer will have responsibilities including those listed below.

· 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 optimisation of services delivered

· Contracts in scope include:

o Facility management, maintenance and repair across all three client Ireland sites - Cruiserath Biologics, Plaza 254 and Shannon Distribution Centre

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.

In addition, key responsibilities will include:

· Overseeing service delivery and maintaining and developing relationships with Service Providers in partnership with company 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.

Requirements:

· The successful candidate must possess 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