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Implement updates to applicable quality system requirements. Working with the R&D team and being responsible for Medical Product (CE Mark and FDA 510k) Design Assurance, Product and Process Validation System, and Risk Management Activities
You help resolve conflicts which may arise as staff endeavour to balance their own duties and responsibilities with the individual's needs and preferences - To lead a team in the development and implementation of effective Quality Assurance and Accreditation systems and processes related to learning and employability services.
Provide technical support in documenting & maintaining the GDD Quality Management System through knowledge & understanding of ISO13485, 21 CFR 820, 21 CFR Part 4 Compliance, & MDD 93/42/EEC, Annex 1 “Essential Requirements” with linkage to Directive 2001/83/EC Medicinal Products for human use, and the recently released Medical Device Directive.
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Reviewing the work of junior team members to ensure quality, thoroughness, completeness and completion of assignment tasks within agreed time frames - Position / job title: Assistant Manager/Senior Associate - Specialism: Risk Assurance Solutions - Industry: Internal Audit - Location: Spencer Dock, Dublin
Permanent Vacancy in Merit Medical Ireland Ltd - Quality Assurance Engineer - Provide quality support to assigned production departments ensuring product manufactured conforms to quality standards and specifications, GMP's of all medical device regulatory agencies.
Will provide ongoing supervision of compliant subsystems of the site Quality Management System. Joining Ipsen means being part of a Group which offers motivating challenges and a wealth of opportunities in APID, Manufacturing, Quality, Engineering, Supply Chain, Sales, Marketing, Finance and HR.
To support the Quality Assurance Manager and Quality Assurance Team Lead with the development, implementation and maintenance of the quality standards and systems to ensure that products comply with Marketing Authorisations, documentation, specifications and cGMPs. Operation of SAP (ERP System) Quality function as per procedures.
NO AGENCY HELP NEEDED AT THIS TIME]]> The successful applicant will support the Quality Assurance Manager with the development, implementation and maintenance of the quality standards and systems to ensure that products comply with documentation, specifications and applicable regulations
Our Client a leading Pharmaceutical company based in Co. Wicklow is looking for Quality Assurance Manager responsible for the implementation of the Pharmaceutical Quality System.
Our client who is multinational medical device company based in Galway, now have a vacancy for a Quality Assurance Engineer. Provide quality support to assigned production departments ensuring product manufactured conforms to quality standards and specifications, GMP's of all medical device regulatory agencies.
Maintain the Pharmaceutical Quality System to include: Personnel, Premises & Equipment, Production, QC, Outsourced activities, Complaints & Product Recall, Self-Inspection - Manage and co-ordinate all Commercial Quality Assurance activities for the company - Support the Head of Quality with the quality department function
While our client-facing professionals can be required to travel regularly, and at times be based at client sites, our flexible working arrangements can help you to achieve a lifestyle balance. Provision of high quality deployment and support service for audit tools including piloting and UAT
Its primary objectives are to ensure continued quality of service delivery, optimal usage of infrastructure resources, and efficient delivery of Business led projects and full exploitation of all new market driven opportunities.
IT Carlow are currently seeking Associate Lecturer - Quality Assurance and Operational Management. Applicants must have a relevant Honours Degree (First or Second class), or equivalent, plus a relevant higher qualification (Masters or PhD) or equivalent professional qualification. Candidates will also have at least three years relevant postgraduate experience.
Assuring Quality standards are maintained and assist with the implementation of and compliance to the Quality Management program and for Supporting company goals, objectives, policies, procedures, quality systems, and FDA regulations. Senior Quality Assurance roles with an expanding multinational who can offer progression opportunities
Our Client a large manufacturing facility with Headquarters in Drogheda currently have the requirement of a Quality Assurance Administrator for a 3-6 month contract.
Department: Quality SUMMARY: The purpose of the position is to provide Design Control Quality Engineering services for Continence products in the Ballina Continence Care Plant and so contribute to the growth and profitability of Hollister. Act as a core team member on Continence NPC projects representing Quality Management
Assist with quality control functions including incoming inspections, process controls/audits - Ensure all relevant documentation is prepared and updated in line with all quality and regulatory guidelines and promotes full compliance i.e. Finished Goods Specifications - Responsible for the Quality Control hold area
Leads and/or facilitates compliance and improvement activities associated with the Company quality system (e.g. CAPA). ESSENTIAL SKILLS / EXPERIENCE: Minimum Bachelor's Degree in Engineering, Science or related technical field, and a 3 years minimum QA, Quality System or regulatory experience in the medical industry a prerequisite.
Reporting to the Quality Manager, the Quality Assurance Officer will provide support with document control, internal audits, intranet updates, and maintain the Quality Management Systems.
Lead the effective implementation of all quality requirements across all 5 Global Service Centers (GSCs) together with PLS Global practice leads, senior SMEs, Quality Leads at GSCs and Divisional Quality to ensure that systems and business processes are compliant with Novartis Quality and regulatory requirements.