# QA Contractor (1.5 Days) at Pale Blue Dot®

> Hybrid · Ireland · Unspecified · QA / Test · open. Source: https://alderhq.app/jobs/recruitee%3Apalebluedotrecruitment%3A2816476 (read 2026-11-09).

## Facts (observed)

- Company: [Pale Blue Dot®](https://alderhq.app/companies/pale-blue-dot-recruitment)
- Location text: Clare, Munster, Ireland
- Where it can be done from (inferred): Hybrid · Ireland (evidence: "Location: Clare, Munster, Ireland")
- Posted: 2026-11-05 (4 days ago)
- First seen by alder: 2026-11-07 · last verified: 2026-11-08
- Reposted: 0 times · edited: 0 times
- Apply on the employer's site: https://palebluedotrecruitment.recruitee.com/o/qa-contractor-15-days

## Pay and sponsorship

- Posted pay: not posted
- Market band for similar posted roles (Ireland, n 3): p25 €36k, median €50k, p75 €52k

## Description (the employer's text)

Pale Blue Dot® Recruitment is recruiting an experienced Quality Assurance Contractor for an established medical device company with mature product lines. You’ll oversee the company’s existing quality management system, support compliance with ISO 13485 and EU MDR, and make sure customer quality enquiries are answered promptly.

The assignment is expected to start in January 2027 and continue on an ongoing basis. The working days are flexible. The anticipated split is one day onsite in Shannon and half a day remotely, with scope to reverse that arrangement by agreement.

### Responsibilities

Review and maintain the existing medical device quality management system in line with applicable ISO 13485 and EU MDR requirements.

Identify any gaps in the system and follow up on agreed actions.

Coordinate timely responses to customer quality enquiries.

Support responses to FDA queries or concerns relating to medical devices entering the US market.

Work with the company’s existing QA consultant and internal team on quality and regulatory matters.

### Requirements

Experience managing or overseeing a quality management system in the medical device industry.

Practical knowledge of ISO 13485 and the EU Medical Device Regulation (MDR).

Experience with US FDA medical device quality system requirements is essential, along with the ability to support responses to FDA queries.

Strong written communication and the ability to work independently within a part-time schedule.

The role may suit an experienced QA professional looking to reduce their hours, return to quality after a career break, or add a regular assignment to their consulting work.

### Pale Blue Dot® Recruitment – The Experts in STEM Workforce Solutions

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Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/recruitee%3Apalebluedotrecruitment%3A2816476 and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.