Quality Specialist/DRP at United Drug
Limerick, County Limerick, Ireland -
Full Time


Start Date

Immediate

Expiry Date

03 Dec, 25

Salary

0.0

Posted On

03 Sep, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Lean Principles, Communication Skills, Regulatory Affairs, Life Sciences, Training, Sap

Industry

Pharmaceuticals

Description

QUALITY SPECIALIST/DRP

Our people make the difference. Here at PHX Ireland, we strive to be a place for everyone - where each and every one of us can be our true, authentic selves, every single day.
For us, individuality sparks new ideas, shapes new approaches and brings us powerful new perspectives. It’s the heartbeat of our innovation, creativity, and success. Which is why, at PHX Ireland, we don’t just embrace our differences - we celebrate them.
Across United Drug, McCabes Pharmacy, and TCP Homecare, in every location and every role, the way we work makes us who we are - and that’s something we are really proud of. Which is why we’ve summed up our ethos in our six PHX Ireland values; Customer focused, Quality driven, collaborative, ambitious, innovative, and inclusive.

QUALIFICATIONS AND EXPERIENCE

  • Degree in Pharmacy, Life Sciences, or a related field (Pharmacist registration may be required in some jurisdictions).
  • Minimum 3 years’ experience in pharmaceutical wholesale distribution, quality assurance, or regulatory affairs.
  • In-depth knowledge of EU GDP guidelines and relevant national regulations.
  • Experience with Quality Management Systems (QMS) and regulatory audits/inspections.
  • Strong attention to detail, organization, and communication skills. Desirable:
  • Experience with ISO 9001:2015, Lean principles, or continuous improvement projects.
  • Familiarity with SAP or other ERP systems.
  • Certification or training related to GDP or Quality Management.
Responsibilities

OVERVIEW/PURPOSE OF THE ROLE

As Deputy Responsible Person (DRP), the role supports the Responsible Person in ensuring full compliance with EU and HPRA Good Distribution Practice (GDP) guidelines for pharmaceutical secondary wholesale activities, acting as the designated RP in their absence. The position is responsible for maintaining and continuously improving the company’s ISO 9001:2015-certified Quality Management System, conducting audits, managing CAPAs, and ensuring ongoing regulatory compliance. The role also leads lean management initiatives to enhance operational efficiency and reduce waste across quality processes. As an SAP super user, the role provides frontline system support, training, and process optimization to ensure accurate data management and streamlined operations.

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