Facilities Engineer
- Dublin
- Contract
- CAPEX Projects
Would you like to grow your career, whilst contributing to scientific innovations that are transforming patients’ lives? Our client, a globally renowned biotechnology organisation, and voted one of the top 10 best companies to work for in Ireland, is looking to recruit a Facilities Engineer to join their team.
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 optimisation of services delivered
- 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.
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.
If this role is of interest to you, please apply now
The candidate must have the rights to work in the location stated in the job advert.
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I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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