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Search Results for Quality Manager
Job Title. Location Salary Actions

Quality Manager

We’re currently recruiting for an exciting opportunity with a Quality & Compliance Consultancy based in Dublin. This is a key role ensuring compliance with EU Cosmetics Regulation while supporting the release of high-quality products to market. Key Responsibilities: Act as Responsible Person under EU Cosmetics Regulation. Oversee product release and ensure compliance with all regulatory requirements. Manage and audit Contract Manufacturing Organisations (CMOs) to maintain quality standards. Liaise with EU regulatory bodies and ensure timely submissions and...

Location: Dublin,
Quality Manager 		Dublin Not Disclosed

Quality Manager

Quality Manager – High-Growth Medical Device Start-Up – Galway About the Company Our client a rapidly growing, well-funded medical device start-up based in Galway, entering an exciting new phase of operational scale-up. With a high-potential product pipeline and a leadership team experienced in successful start-up growth and commercialization, are building out their core team to support ongoing manufacturing, development, and expansion activities. The Opportunity Client are seeking a hands-on and driven Quality Manager to take ownership of&nbsp%3...

Location: Galway,
Quality Manager 		Galway Not Disclosed

Quality Manager - Medical Devices

Life Science Recruitment has been engaged by our client, a global leader in the medical devices sector, to source a Quality Manager for their state of the art manufacturing facility in Limerick City. This role represents a rare opportunity to join a globally reputed company as it continues to grow it's Irish operation in Limerick. The primary purpose of this role will be to act as the communication line between senior management and a team of Quality Engineers/Techs. A proven track record managing and leading a team within the parameters of a highly regulated manufacturing envir...

Location: Limerick City,
Quality Manager - Medical Devices 		Limerick City Not Disclosed

Quality Manager

Our client an early-stage company developing an innovative medical device technology are looking to expand the team to support its development and manufacturing activities with the recruitment of a Quality Manager. Reporting to the COO the Quality Manager this position will be responsible for quality system, quality aspects of internal manufacturing, oversight of sub-contract manufacturing partners and support of internal projects. Role/ Responsibilities: Maintain company's Quality Management System (QMS) and report on the performance of the QMS to the com...

Location: Galway,
Quality Manager 		Galway Not Disclosed

QA Manager

QA MANAGER Our client a Canadian based early stage pharma company are currently seeking a QA Manager to join their team. Role is with an innovative company who are currently scaling up manufacturing and looking for a strong Quality professional to join them on the journey. Relocation and visa assistance will be provided Role/Responsibilities: • Ensure facility is compliant to GMP expectations for manufacture, storage, distribution, and testing of drug product. • Perform comprehensive oversight related to manufacturing/ packaging comp...

Location: Canada,
QA Manager 		Canada €100000+

Senior Quality Engineer

Job title: Senior Quality Assurance Engineer Location: Oranmore, Galway Benefits: Excellent salary, Income Protection, Life Assurance, Contribution of €2,000 per annum in lieu of health insurance, Pension Scheme, Annual discretionary bonus up to 10%, Educational Assistance, Employee Referral Programme, Cycle to Work Scheme, Sports & Social Activities Role: As a Senior Quality Engineer you will be responsible for implementing and promoting best in class quality assurance through the product lifecycle for my client device. C...

Location: Galway, Galway City,
Senior Quality Engineer 		Galway Not Disclosed

Quality Manager - NPI

Role: Quality Manager - NPI Based in Dun Laoghaire – on site role Benefits: Competitive salary, Healthcare, bonus or share options and Pension contribution, excellent opportunity to expand your career in exciting Medical Device company growing from strength to strength. Company: My client have deep expertise and advanced technologies to continuously innovate their pen needles, insulin syringes and other products. Job Purpose: To provide support for ISO9000/ISO13485 Quality System. Responsible for ensuring adherence to al...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South,
Quality Manager - NPI 		EU Not Disclosed

Quality Manager

Role: Quality Manager - NPI Based in Dun Laoghaire – on site role Benefits: Competitive salary, Healthcare, bonus or share options and Pension contribution Company: My client have leveraged deep expertise and advanced technologies to continuously innovate their pen needles, insulin syringes and other products. They offer an excellent opportunity for anyone looking to grow their career in the Medical Device industry. Job Purpose: To provide support for ISO9000/ISO13485 Quality System. Responsible for ensuring adher...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North,
Quality Manager 		EU Not Disclosed

Senior Quality Engineer

Title: Senior Quality Engineer Location: Dublin 1 (Hybrid working) Company: My client are developing a Best-In-Class minimally invasive solution for severe Tricuspid Regurgitation (TR).It is a clear unmet clinical need, with a significant impact on mortality, cardiovascular events and quality of life. With a prevalence greater than aortic stenosis in the population over 65 years, TR is the next structural heart opportunity. Responsibilities: Support the development, implementation, and maintenance of the QMS in accordance with relevant st...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South,
Senior Quality Engineer 		EU Not Disclosed

Quality Systems Manager

Company: My client are have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. They are committed to helping create healthier communities worldwide through education, outreach and better access to treatment Role: Quality Systems Manager - Senior Location: Newenham Court, Northern Cross, Malahide rd, Dublin 17 Team: 6 direct reports Hybrid working: 2-3 days a week on site per week Benefits: Compe...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South,
Quality Systems Manager 		EU Not Disclosed

Senior Quality Engineer

Title: Senior Quality Engineer Location: Dublin 1 (Hybrid working) Company: My client are developing a Best-In-Class minimally invasive solution for severe Tricuspid Regurgitation (TR).It is a clear unmet clinical need, with a significant impact on mortality, cardiovascular events and quality of life. With a prevalence greater than aortic stenosis in the population over 65 years, TR is the next structural heart opportunity. Responsibilities: Support the development, implementation, and maintenance of the QMS in accordance with relevant st...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South,
Senior Quality Engineer 		EU Not Disclosed

Responsible Person (RP)

Life Science Recruitment are delighted to partner with our client, an internationally established dynamic consultancy, to source an experienced RP to join their professional team of consultants on a permanent full time basis. This role will recquire the successful candidate to work with a portfolio of designated clients to ensure compliance with the requirements of GDP and other relevant guidelines both EU and HPRA & UK (MHRA) They will also ensure that the conditions of the Wholesale Distribution Authorisation are met and that all medicinal products wholesaled, are rece...

Location: Republic of Ireland,
Responsible Person (RP) 		Republic of Ireland Not Disclosed
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Quality Manager Career Profile

Quality Manager


This is a wide role which often requires a Medical Device Quality Systems background and expertise within ISO 13485. Applyling this knowledge to a cutting edge industry is often an attraction for candidates who are used to working in a more manufacturing-orientated environment. A sample spec is below:

Key Responsibilities


  • Initially as a core member of the team which will implement a Global Quality Management System,
  • As required oversee the production of DHF for products to be marketed in the US.
  • As required assist in the preparation of 510k submissions for our client's products and product components. This may also require some involvement in clinical trials.
  • As required develop an understanding of other overseas regulatory requirements (and prepare for submissions where clearance is required.
  • Proactively develop and maintain the Company Quality Management System in accordance with regulatory and corporate requirements.
  • Furthermore seek to improve the efficiency and effectiveness of the Quality System to meet the business strategy of the company.
  • Act as the company representative in any company inspections/audits.
  • Under the direction of the Head of RA/QA take ownership for the co-ordination of specific
  • projects providing specific regulatory and quality services.
  • Oversee design control for specific company products: review and approval of documents,
  • maintain design history file, communicate findings and suggestion for improvements to design group. Ensure documents are produced in accordance with company procedures and check all documents for consistency and accuracy prior to issue.
  • Work with service/manufacturing to ensure adequate quality controls prior to shipping.

Qualifications / Experience

  • Degree level qualification preferred or an equivalent combination of education and experience to operate at this level.
  • Proven RA / QA experience supporting product design control, customer support and production with at strong supervisory experience.
  • Working knowledge of FDA Quality Systems Regulations and ISO 13485:2003 required.
  • Internal audit qualification also preferred. ISO13485 lead auditor qualification preferred but not essential.
  • Experience in medical devices
  • Understanding of QA and Regulatory requirements