qaresources.ie

QA Resources, providing Contract Services to the Pharmaceutical, Medical Device and Healthcare Industry in Ireland

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! Welcome to QA Resources. QA Resources provide a full range of contract services. In quality assurance, compliance and validation to the pharmaceutical. Established in 2003 and based in Ireland, we work with some of the biggest companies in the world on a wide variety of projects. Our people are highly qualified and very experienced. That’s where we excel. Review and Implementation of Quality Systems. Of all phases of drug development.

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QA Resources, providing Contract Services to the Pharmaceutical, Medical Device and Healthcare Industry in Ireland | qaresources.ie Reviews

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Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! Welcome to QA Resources. QA Resources provide a full range of contract services. In quality assurance, compliance and validation to the pharmaceutical. Established in 2003 and based in Ireland, we work with some of the biggest companies in the world on a wide variety of projects. Our people are highly qualified and very experienced. That’s where we excel. Review and Implementation of Quality Systems. Of all phases of drug development.

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QA Resources, providing Contract Services to the Pharmaceutical, Medical Device and Healthcare Industry in Ireland | qaresources.ie Reviews

https://qaresources.ie

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! Welcome to QA Resources. QA Resources provide a full range of contract services. In quality assurance, compliance and validation to the pharmaceutical. Established in 2003 and based in Ireland, we work with some of the biggest companies in the world on a wide variety of projects. Our people are highly qualified and very experienced. That’s where we excel. Review and Implementation of Quality Systems. Of all phases of drug development.

INTERNAL PAGES

qaresources.ie

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Regulatory – Active Pharmaceuticals Ingredients (API), Medical Devices, Conversion of site DMFs to CTD format, Application and successful granting of Certificates of Suitability

http://www.qaresources.ie/kelly-rya.php

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! GMP Training and Coaching. Emer is a Biochemistry graduate with extensive experience in the biotech,. Medical device and pharma sectors in a variety of roles. She is a Lead. Auditor and Trainer and has a Certificate in Quality Assurance of. Pharmaceutical Packaging Components. Emer has led the Compliance Monitoring. Programme for a biotech company while providing ongoing support and coaching. Based in the Mid West. Genzyme have employ...

2

Q.A. Compliance & Validation Professional, with over 30 years pharmaceutical & medical device experience, Margaret is a highly qualified Quality Assurance, Regulatory Affairs and Validation Specialist

http://www.qaresources.ie/margaret-foley.php

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! GMP Training and Coaching. QA Compliance and Validation Professional. Quality System implementation including:. Preparation of Quality Manual and Standard operating procedures. Investigation of Customer Complaints, Deviations and OOS. CGMP and Quality System Training. Internal and Supplier Audits (Lead Assessor). Preparation and Support during Regulatory Inspections. Corrective and Preventive Actions. Examples of Projects Completed.

3

PhD Chemist with much experience as a development chemist implementing PAT solutions in API processes and as part of process improvement and optimisation projects

http://www.qaresources.ie/deirdre-cahalan.php

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! GMP Training and Coaching. Audit and review of batch and quality documentation and specifications. Compilation of PQRs/APRs and Annual Reports. Liaising with regulatory agencies. Complaint and Failure Investigation Quality System management. Internal and vendor quality auditing. Assisting with 3. Managing Plant Master Files and Dossiers. Back to QA Resources Team. What our clients say! QA Resources are a highly professional, very capa...

4

BSC (Hons) in Microbiology, Higher Diploma in Education & Diploma in Pharmaceutical Manufacturing Technology

http://www.qaresources.ie/catherine-obrien.php

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! GMP Training and Coaching. Prior to establishing Q.A. Resources in January 2002, Catherine worked as a Quality Systems Manager, Product Release Manager, QP, Microbiologist and Validation Co-ordinator within the pharmaceutical and cosmetics industries. In addition to managing Q.A. Resources, she continues to work in various varied roles on a contract basis within the pharma, medical device and API sectors. Back to QA Resources Team.

5

Observing the highest standards in GMP, she is an IRCA Certified Lead Assessor with a quality systems auditing background. She has excellent communication skills and a professional approach

http://www.qaresources.ie/catherine-kilbane.php

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! GMP Training and Coaching. Understanding of statistical techniques, in particular statistical sampling plans, process capability and gauge R&R. IRCA Certified Lead Assessor. Trained in the requirements of ISO 13485:2003, Medical Device Directive, SPC, Regulatory Affairs and validation issues. Based in Tipperary and available to work in the Munster and Midlands regions. Available from end December 2016. Back to QA Resources Team. Eamon...

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QA Resources, providing Contract Services to the Pharmaceutical, Medical Device and Healthcare Industry in Ireland

Successful ISO 9001:2008 Audit. Introducing GDP Genius and EHS Genius! Welcome to QA Resources. QA Resources provide a full range of contract services. In quality assurance, compliance and validation to the pharmaceutical. Established in 2003 and based in Ireland, we work with some of the biggest companies in the world on a wide variety of projects. Our people are highly qualified and very experienced. That’s where we excel. Review and Implementation of Quality Systems. Of all phases of drug development.

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