Facilities & Engineering Compliance Senior Associate
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Job Type | Contractor |
Location | Dublin |
Area | Dublin, Ireland |
Sector | Engineering |
Start Date | |
Advertiser | Darcy Ainscough-Denton |
Telephone | +353 1 574 6266 |
Job Ref | 1003035 |
Job Views | 135 |
- Description
- Team Horizon is seeking a Facilities & Engineering Compliance Senior Associate (initial 12-month contract) for our client who are a global biopharmaceutical company based in South Dublin. The person in this position will be the supporting throughout the client site with specific responsibilities within the Facilities Department. It will be a key member of the overall organisation at the site. The position will report to the Sr. Mgr. Engineering responsible for the Facilities Department.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Pest Control System Owner.
Managing pest control vendor visits.
Ensuring layout drawings are keep up to date.
Analysing vendor reports and creating monthly compliance reports.
Represent the client on the global network team.
Accountable for overall documentation compliance for the department.
Tracking safety metrics INCA’s/CAPA’s.
Quality GMP documents.
SOP’s.
Compliance Reports.
Deviations.
Access control system owner.
Assist with quarterly compliance reviews and CDOC’s updates.
Ensuring layout drawings are keep up to date.
Assist with department finance in the form of raising purchase requestions.
Support the general coordination within the department.
Collation of capacity data for site.
Participant in Zone inspection.
Development and management of department oversight audit on the IFM program.
Drawings review and red line for updates.
Development and assistance of department projects.
Management/updates of facilities share point.
Provide support with the completion of deliverables as required.
Day to day management of communication and any other tasks/projects assigned as per manager’s request.
Any other duties as assigned.
What you need to apply:
Bachelors’ degree or similar relevant qualification.
At least 1-3years experience in a GMP, Biopharmaceutical manufacturing plant.
Experience in pharma industry.
Ability to build working relationships and effectively partnerships at all levels in the organization.
Excellent oral and written communication, facilitation, organizational and planning skills.
Proactive, self-starter with the ability to take on several projects at one time.
Basic computer skills (MS Office literate).
Good Manufacturing Practices and Good Documentation Practices is a must.