Search Results: 33 vacancies
...structured approach to resolving day to day engineering issues typical of a live manufacturing environment.
* Knowledge of cGMP and regulatory requirements relating to the Healthcare industry is required.
* Demonstrated project management skills, including the ability to...
Sligo, Co. Sligo
26 days ago
...discipline.
* 3 years plus validation experience in pharmaceutical, diagnostics or medical device industry & knowledge of cGMP and regulatory requirements
* Strong communication (written and oral), presentation and troubleshooting skills required.
* Effective...
County Sligo
2 days ago
Role
To coordinate the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements. Co-ordination, implementation and active participation in the site Validation Program.
Responsibilities:
* Ensure...
Sligo, Co. Sligo
22 days ago
£ 43 - 55 per hour
...vendor package owner for large construction projects
· Great communicator and team player
· Knowledge of risk based (ASTM E2500) approach to CQV
· Experience of working to deadlines within a time critical environment
Working knowledge of US FDA & EU GMP regulatory requirements
County Sligo
22 days ago
...Experience of start-ups and/or new product introductions to pharmaceutical facilities is desirable.
~ Detailed Knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry preferred.
~ Demonstrated project management skills, including the ability to...
...manufacturing equipment is maintained to meet the output and yield requirements.
Adhering to all relevant policies relating to Quality and regulatory
Supervision of external contractors carrying out work onsite
Required to undertake specific investigations, and equipment...
...Validation/Quality experience in medical device plastics processing, moulding or assembly operations.
3+ years of knowledge of cGMP and regulatory requirements relating to the medical device industry.
Strong communication (written and oral), presentation and troubleshooting...
...additional offices in Galway, Limerick, Leinster and Florida USA.
We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM ’s and Technology providers.
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...TPM Managers, track, and drive audit results, including corrective actions, and any required follow-up.
Support third party and regulatory agency inspections as needed.
Participate in relevant Division and AQR communities of practice with ownership change mgt of disseminated...
...The Biologic’s Technician will work as a team member to support biologics operations in pharma operations in line with all safety, regulatory and organizational requirements.
Are you intrigued? Do you want to learn more?
A snapshot of your key responsibilities as a Biologics...
...Provide technical input to the transfer of microbiological test methods to the site.
Act as the sites’ sterility assurance SME during regulatory inspections.
Through the use of training and a purposeful presence on the operations floor, ensuring that the sites practices...
...advantage.
Innovative and Continuous Improvement mindset. The position impacts directly on product quality and thus the financial and regulatory exposure of decisions could be significant.
The position has scope for decision making within the confines of agreed...
...productivity.
Resolve daily operational issues and implement procedural changes to enhance throughput.
Ensure compliance with regulatory and GMP requirements, including record-keeping, inspection standards, and validation protocols.
Implement corrective and preventative...
€35k - €55k per annum
...principles and a strong technical focus
REVIT + AutoCAD skills.
Word, Excel, Power Point, MS Project
Understanding of the Irish regulatory and policy issues.
The ability to work closely in partnership with clients and contractors and other members of design teams....
...of this role is to coordinate the development and maintenance of the company's validation program in compliance with all applicable regulatory and company requirements along with the co-ordination, implementation and active participation in the site Validation Program....
...relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements.
Are you intrigued? Do you want to learn more?
A snapshot of your key responsibilities as a...
....
Skills Brief:
Significant experience of over 3 years Commissioning Qualification in a project environment.
Experience in regulatory and industry standards for GMP, cGMP and GDP
Excellent technical writing skills including deviation reports and validation reports...
...additional offices in Galway, Limerick, Leinster and Florida USA.
We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers.
Find out more about working at SL Controls , our...
...Sciences company located in the North West of Ireland . The QA Specialist ensures product manufacturing complies with GMP and Regulatory standards. Responsibilities include validating facility, equipment, and utilities, as well as reviewing and approving validation...
...Transformation and Innovative culture on-site.
Responsibilities:
Ensure the necessary controls are in place to ensure excellence in regulatory, safety and environmental compliance.
Ensure department operates compliantly with AbbVie Global QA/IT policies.
Establish with...
