Search Results: 202 vacancies
€40k - €50k per annum
...URGENT! IT Systems Administrator : Limerick
I am partnering with this leading Irish Manufacturing comopany in their search for an IT Systems Administrator who will be responsible for IT Systems across their manufacturing plant in Limerick.
You will be responsible for...
...IT Systems Administrator
Permanent position available with a considerable portfolio of works for the next 5+ years
To build your career by assisting in the delivery of ‘leading edge’ engineering projects.
To work with a vibrant, agile and multi-functional team...
...Quality Management System Specialist
RK21220
Contract – 11 months
Cork
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading...
...Cork: (***) ***-**** | Dublin: (***) ***-****
Join our team as the Site Planning, Scheduling, and Systems Manager, where you'll play a pivotal role in orchestrating the site's planning, scheduling, and maintenance systems. Your day-to-day will involve managing the...
£500 per day
...issues at site & escalating when needed.
Report malfunctions of systems along with proposed solutions for improving system efficiencies.... ...chain, procurement, etc) is preferred.
Experience of working in a GMP environment.
Ability to: Set up, modify, service, adjust, and make...
...quality medical devices products.
Adherence to COOK Quality system procedures and all associated manufacturing documentation which is... ...manufacture & shipment of product.
Ensure that a high standard of GMP and housekeeping is maintained in all manufacturing areas....
...to design, develop, implement, and maintain SCADA, PLC, and HMI systems in a Pharmaceutical facility
Key Responsibilities:
Develop... ...equipment and processes.
Serve as SME for process automation in GMP settings.
Manage and maintain PLC-based Control Systems, BMS,...
...engineering.
* 4 years’ experience in relevant engineering / asset management / maintenance leadership role.
* Prior experience in a GMP or medical device manufacturing environment.
* Prior experience in equipment and process validation activities.
* Good project...
...initial response to follow-up.
• Establish and maintain safety, GMP and Environmental Standards.
People Management:
• Ensures... ...good organisational skills.
• Proven ability to make good use of systems, procedures & processes.
• Demonstrated track record in effective...
...oversight of and guidance on capital projects
-Maintenance of all aspects of GMP compliance for the area(s) of responsibility
-Establishment, maintenance and management of a control system for the specific Quality System(s)/Program
-Interpretation and application of...
...contractors in a regulated environment.
− Management of the maintenance system, procedures, and improvement projects associated with the water... .../Industrial Chemistry/Process Engineering
− Experience with GMP Formulations process’ in a Medical Device or Pharmaceutical...
...they do.
Duties:
Batch Record Review & material release to ensure compliance with GMP requirements.
Carries out tasks related to the administration of event management systems including Review & Approval of Event, Deviations, and Customer complaints.
Carries out...
...VALIDATION SPECIALIST will have experience in the execution of cleaning validation protocols, experience on writing and approving Deviations/ GMP documents and Technical writing experience in writing site reports.
Role of this position
Taking Cleaning Validation samples...
...qualification in production, manufacturing or mechanical engineering.
4 years' experience in relevant engineering role
Prior experience in a GMP or medical device manufacturing environment
Prior experience in equipment and process validation activities
N.B. It is essential...
...maintaining documentation to ensure effective and efficient application of GMP.
Documentation within this process includes, but is not... ...of the documentation lifecycle and associated electronic systems. Performs departmental tasks under limited supervision.
Essential...
...position.
Role of this position
Execution of SIP/ cleaning and continuing validation protocols.
Writing and approving Deviations/ GMP documents
Technical writing experience in writing site reports.
Generate/review/Approval of SIP/ CIP protocols
Generation of...
...in production, manufacturing or mechanical engineering.
4 years' experience in relevant engineering role.
Prior experience in a GMP or medical device manufacturing environment.
Prior experience in equipment and process validation activities.
N.B. It is essential...
£56.11k - £69.06k per annum
...in Electronic engineering
A key component of this role is solid experience in Digital design
FPGA Experience
Exposure to embedded systems is a huge bonus
A background in product developoment and manufacturing Benefits:
Bonus
Competitive salary
Healthcare
Lots of opportunities...
£32.8k - £34.53k per annum
...and it has an outstanding reputation for excellence through its unrivalled pre and post-sales support, including initial site surveys, system design, installation & commissioning, preventative maintenance, training, remote monitoring and technical support.
The successful...
...projects after this project? If so, please read on...
Responsibilities:
* Lead the commissioning process for protection and control systems in 220kV substations.
* Conduct thorough testing of protection relays, control systems, and associated equipment to ensure...