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Teleflex
3.7
Regulatory Affairs Specialist
Athlone, Co. Westmeath
€42K - €57K (Glassdoor est.)
Participate in project meetings to provide regulatory inputs during the planning, execution and closure of the projects.…
30d+
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Regeneron
3.6
Commercial HCP Engagement Manager
Dublin, Co. Dublin
€53K - €88K (Glassdoor est.)
In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k)……
2d
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Baxter
3.6
Releaser, QA
Dublin, Co. Dublin
€43K - €53K (Glassdoor est.)
Support the timely release of equipment, utilities, facilities, and computer systems following the execution of test protocols. 2 Days a Year to Volunteer.…
8d
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Teleflex
3.7
HR Administrator
Athlone, Co. Westmeath
€27K - €42K (Glassdoor est.)
Assist with employee relations matters, including preparing documentation, note-taking, and supporting processes such as grievances, disciplinaries, and appeals……
24d
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Regeneron
3.6
Associate Director, Commercial Launch & Project Management
Dublin, Co. Dublin
€110K - €130K (Glassdoor est.)
In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k)……
18d
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BioMarin Pharmaceutical
3.3
Recruiter (TEMPORARY)
Cork, Munster
€32K - €67K (Glassdoor est.)
Experience of managing full 360 degree recruitment process is essential. You will apply strong technical expertise (such as strategic sourcing, candidate and……
30d+
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Vantive
4.0
AI Implementation Engineering Manager
Castlebar, Co. Mayo
€44K - €78K (Glassdoor est.)
In addition, you will play a key role in a global IT system migration project, supporting the transition of legacy platforms.…
30d+
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Teleflex
3.7
Senior Finance Analyst FTC
Athlone, Co. Westmeath
€45K - €68K (Glassdoor est.)
Coordinate period financial reviews of strategic projects with the execution team to ensure proper financial forecasting and monitoring of the projects.…
24d
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Vantive
4.0
Projects Engineering Manager
Castlebar, Co. Mayo
€51K - €65K (Glassdoor est.)
Coordinate engineering team in planning and executing complex project activities with accountability for successful completion of assigned deliverables to……
30d+
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Vantive
4.0
Quality Operational Excellence Engineer
Castlebar, Co. Mayo
Training and Development: Coach and mentor laboratory personnel on Lean and continuous improvement principles to sustain a culture of excellence.…
30d+
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Vantive
4.0
Operational Excellence Engineer
Castlebar, Co. Mayo
€48K - €73K (Glassdoor est.)
Training and Development: Coach and mentor peers on Lean principles and other operational excellence tools. The role requires a blend of technical proficiency,……
30d+
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Teleflex
3.7
Senior Quality Engineer
Cork
Lead, motivate and mentor cross functional teams to ensure that project milestones and results are achieved in line with business needs.…
30d+
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Teleflex
3.7
Senior PLM Engineer Analyst
Athlone, Co. Westmeath
€50K - €70K (Glassdoor est.)
Support and execute formal test cycles ensuring end‑to‑end compliance and functionality. This role combines hands‑on PLM system expertise, ownership of PLM user……
30d+
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Teleflex

3.7

Regulatory Affairs Specialist

Athlone, Co. Westmeath

€42K - €57K (Glassdoor est.)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Date: May 21, 2026

Location: Athlone, L, IE

Company: Teleflex

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.

Position Summary

Support the regulatory activities which lead to and maintain regulatory compliance and approval for Teleflex Medical products in the EMEA region

Principal Responsibilities

Key responsibilities will include (but are not limited to) the following:

Ensure compliance with EMEA regulatory requirements and applicable regulatory standards.
Coordinate and support regulatory and product registration activities for the EMEA region, including new product registrations, license amendments, renewals, and maintenance of existing approvals.
Prepare, compile, review, and maintain regulatory submission files and associated documentation for product registrations, tender applications, and other international market requirements.
Review Change Orders, change control documentation, and related technical documentation to assess potential regulatory impact on EMEA and regulatory submissions and approvals.
Provide timely regulatory affairs input to cross-functional projects, including new product introductions, product changes, process changes, and other business or regulatory initiatives.
Collaborate with Business Units, regional partners, distributors, and internal functional teams to support efficient and timely product registrations, and ongoing regulatory compliance.
Research and respond to regulatory queries from internal stakeholders and external parties, including distributors, and customers, and prepare supporting information for product shipment and market access activities.
Liaise with internal departments to ensure that accurate supporting technical, scientific, and quality data are generated, reviewed, and provided in a timely manner for regulatory submissions and compliance activities.
Support and/or coordinate Internal Part Number (IPN) reviews and Market Registration (MR) activities for the EMEA region, including creation, review, maintenance, and coordination of associated records.
Support Purchased Finished Device (PFD) verifications in accordance with applicable EU MDR requirements.
Support regulatory inspections, internal audits, and external audits as required.
Ensure ongoing Quality System compliance through adherence to internal procedures and applicable external regulatory requirements, and support alignment of local regulatory procedures with global procedures.
Keep informed of new and evolving regulatory requirements and developments relevant to the EMEA region and broader international markets.
Provide guidance, support, and day-to-day coordination for junior team members, where applicable.
Adhere to Teleflex’s Code of Ethics and all company policies, rules, procedures, and housekeeping standards.
Support other duties and regulatory activities as assigned by management.

Education / Experience Requirements

Degree in a relevant Science or Engineering discipline required.
3 years medical device industry experience within quality or regulatory essential.
Technical writing expertise.
Basic knowledge and understanding of EU and international medical device regulations, standards and guidance documents.
Project Management skills and experience.

Specialized Skills / Other Requirements

Self-driven and ability to work independently and/ or as a team player.
Approachable and enthusiastic. Flexible and adaptable.
Able to work on own initiative and as a team player.
Good organisational skills with cultural awareness and sensitivity.
Good judgment and problem-solving ability & capable of understanding the impact of decision making on both Teleflex and customers.
Excellent Communication skills both written and verbal.
Interface with various departments as applicable for the project to ensure all regulatory deliverables are achieved.
Communicate concerns effectively to the RA Manager and project teams to ensure that they are addressed.
Participate in project meetings to provide regulatory inputs during the planning, execution and closure of the projects.
Pharmaceutical and/or Drug/ Device Combination device experience and Clinical expertise an advantage

Teleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community.
If you require accommodation and support to apply for a position, please contact us at talent.emea@teleflex.com.
Diversity fosters innovative thinking and entrepreneurship and that’s what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror the patients we serve and the communities we operate in. Our approach is simple, we embrace everyone and want them to feel they belong here. We are building a culture where all employees can bring their best and unique selves to work. If that appeals to you, we would love to hear from you. Come join a company where diversity is sought out and inclusivity is how we progress.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

See company reviews

Base pay range

The minimum salary is €42K and the max salary is €57K.

€42K – €57K/yr (Glassdoor est.)

€49K

/yr Median

Athlone, Co. Westmeath

If an employer includes a salary or salary range on their job, we display it as "Employer Provided". If a job has no salary data, Glassdoor displays a "Glassdoor Estimate" if available. To learn more about "Glassdoor Estimates," see our FAQ page.

Working here doesn’t have to be a secret

3.7

Recommend to a friend
Approve of CEO
CEO: Stuart Randle
8 Ratings

Teleflex

3.7

Regulatory Affairs Specialist

Athlone, Co. Westmeath

€42K - €57K (Glassdoor est.)

Teleflex

3.7

Regulatory Affairs Specialist

Athlone, Co. Westmeath

€42K - €57K (Glassdoor est.)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Date: May 21, 2026

Location: Athlone, L, IE

Company: Teleflex

About Teleflex Incorporated

Position Summary

Support the regulatory activities which lead to and maintain regulatory compliance and approval for Teleflex Medical products in the EMEA region

Principal Responsibilities

Key responsibilities will include (but are not limited to) the following:

Ensure compliance with EMEA regulatory requirements and applicable regulatory standards.
Coordinate and support regulatory and product registration activities for the EMEA region, including new product registrations, license amendments, renewals, and maintenance of existing approvals.
Prepare, compile, review, and maintain regulatory submission files and associated documentation for product registrations, tender applications, and other international market requirements.
Review Change Orders, change control documentation, and related technical documentation to assess potential regulatory impact on EMEA and regulatory submissions and approvals.
Provide timely regulatory affairs input to cross-functional projects, including new product introductions, product changes, process changes, and other business or regulatory initiatives.
Collaborate with Business Units, regional partners, distributors, and internal functional teams to support efficient and timely product registrations, and ongoing regulatory compliance.
Research and respond to regulatory queries from internal stakeholders and external parties, including distributors, and customers, and prepare supporting information for product shipment and market access activities.
Liaise with internal departments to ensure that accurate supporting technical, scientific, and quality data are generated, reviewed, and provided in a timely manner for regulatory submissions and compliance activities.
Support and/or coordinate Internal Part Number (IPN) reviews and Market Registration (MR) activities for the EMEA region, including creation, review, maintenance, and coordination of associated records.
Support Purchased Finished Device (PFD) verifications in accordance with applicable EU MDR requirements.
Support regulatory inspections, internal audits, and external audits as required.
Ensure ongoing Quality System compliance through adherence to internal procedures and applicable external regulatory requirements, and support alignment of local regulatory procedures with global procedures.
Keep informed of new and evolving regulatory requirements and developments relevant to the EMEA region and broader international markets.
Provide guidance, support, and day-to-day coordination for junior team members, where applicable.
Adhere to Teleflex’s Code of Ethics and all company policies, rules, procedures, and housekeeping standards.
Support other duties and regulatory activities as assigned by management.

Education / Experience Requirements

Degree in a relevant Science or Engineering discipline required.
3 years medical device industry experience within quality or regulatory essential.
Technical writing expertise.
Basic knowledge and understanding of EU and international medical device regulations, standards and guidance documents.
Project Management skills and experience.

Specialized Skills / Other Requirements

Self-driven and ability to work independently and/ or as a team player.
Approachable and enthusiastic. Flexible and adaptable.
Able to work on own initiative and as a team player.
Good organisational skills with cultural awareness and sensitivity.
Good judgment and problem-solving ability & capable of understanding the impact of decision making on both Teleflex and customers.
Excellent Communication skills both written and verbal.
Interface with various departments as applicable for the project to ensure all regulatory deliverables are achieved.
Communicate concerns effectively to the RA Manager and project teams to ensure that they are addressed.
Participate in project meetings to provide regulatory inputs during the planning, execution and closure of the projects.
Pharmaceutical and/or Drug/ Device Combination device experience and Clinical expertise an advantage

See company reviews

Base pay range

The minimum salary is €42K and the max salary is €57K.

€42K – €57K/yr (Glassdoor est.)

€49K

/yr Median

Athlone, Co. Westmeath

Working here doesn’t have to be a secret

3.7

Recommend to a friend
Approve of CEO
CEO: Stuart Randle
8 Ratings

Are you open to new opportunities?

14 Project Manager - Patient Recruiter jobs in Ireland

Position Summary

Principal Responsibilities

Education / Experience Requirements

Specialized Skills / Other Requirements

Base pay range

Working here doesn’t have to be a secret

Position Summary

Principal Responsibilities

Education / Experience Requirements

Specialized Skills / Other Requirements

Base pay range

Working here doesn’t have to be a secret