Average salary: €32,500 /yearly
More statsSearch Results: 82 vacancies
...a global healthcare leader, is seeking to hire an Inventory Controller to join their team in Sligo. This is an initial 6-month contract... ...to work are essential as the role involves a high level of documentation.
Previous experience in a diagnostic Manufacturing/Warehouse...
...Job Title
Control Systems Engineer – Sligo
The Role
Control Systems Engineer
Sligo
Onsite role
Permanent or Contractor... ...needs.
Set complex design and process requirements.
Complete documentation in a timely manner and in accordance with business standards....
...support, administration, installation, and issue resolution for GxP controlled laboratory and Business Technology Solution (BTS) systems,... ...Solution (BTS) projects.
* Create and maintain system documentation including procedures, work instructions system design specifications...
..., Project Engineering, and QA to ensure that all manufacturing control systems meet global and local compliance requirements, end user... ....
Manage computer system validations and approve associated documentation and specifications.
Generate and deliver training materials...
...Project Engineering and QA to ensure that all manufacturing and control systems are fit for purpose and meet the global and local... ...and improvements.
Manage validations and approve associated documentation and specifications.
Lead team operational excellence activities...
...and utilities, as well as reviewing and approving validation documentation . This individual contributor role requires a self-starter with... ..., facilitating collaboration with departments like Quality Control, Manufacturing, Engineering, and Technical Services.
Overview...
...and implementation of corrective actions.
Creation, review and approval of various quality documents and test data.
Management of validation exception events and change control processes.
Maintenance and tracking of validation equipment, if applicable.
Performing...
...and transfer a well understood, robust, fit-for-purpose process control strategy for each new product introduction (NPI).
Author gap... ...any new equipment.
Author scientific reports and technical documentation and presentations to document and communicate project status to...
...Work with external medical/occupational health resources to identify, control and provide information to employees on site occupational health hazards
Maintain records of all relevant H&S documentation, reports, files, forms, etc. using the company's software and a suitable...
...Power management – configure and maintain PDU, complete necessary documentation, and adjust rack power distribution as needed.
Maintain... ...Facilities and building infrastructure services.
Access control and surveillance system.
Consumable stock control and procurement...
...bring concept to market, including essential product and process documentation
Uses a science-based approach to develop processes, process... ...plans, FMEAs, validation protocols, validation reports, control plans and test method validations supported with appropriate statistical...
...This role will support a long term expansion project for an SL Controls client as the client experiences major growth over the next number... ....
Key Responsibilities:
Prepare, execute and report on CQV documentation
Complete field verifications during static and dynamic (...
€ 15.44 - 16.06 per hour
...company.
Inspect and test products and check statistical process control (SPC) outputs to ensure products are manufactured in... ...requirements of the Medical quality system.
Complete all production documentation as per Medical quality system.
Actively participate in work...
...validation protocols & reports
Managing & coordinating validation documentation (risk assessments, traceability matrices)
Managing &... ...develop and improve upon industry leading technology solutions. SL Controls offers a supportive environment committed to employee development...
...into the creation and maintenance of area SOPs and batch records.
Perform and document operations in accordance with cGMP’s.
Perform environmental monitoring.
Contamination control within cleanroom environments
As the company is a start-up, flexibility will be...
...focus on workflow, S95 & S88 standards and integration from the control layer to MES in pharma & bio-pharma industries
Engage in... ...relevant to MES.
Validate new processes and generate technical documentation for your areas of responsibility.
Uphold compliance with Corporate...
...for both NPI and commercial processes.
Development of process control recipes for NPIs and optimization of existing commercial... ...project start-up.
Development and update of batch and cleaning documentation for NPIs
Preparation of feasibility studies and operating budgets...
...its production schedule targets in for the Manufacture of Cals/Controls, bulks & diluents.
Carry out operations such as:
Solution... ...carry out operations in the Solution Prep areas, ensuring that all documentation is complete and compliant.
Carry out operations in a safe...
...support, administration, installation, and issue resolution for GxP controlled laboratory and Business Technology Solution (BTS) systems,... ...Solution (BTS) projects
· Create and maintain system documentation including procedures, work instructions system design...
...standards and cGMP procedures.
• Review and approve product change controls.
• Liaise with suppliers and clients on quality related... ...authorities.
• Conduct internal audits and compilation of associated documentation.
• Support and assist in the preparation for customer and...