On Demand Quality Administrator at Uniphar Group PLC
Citywest, County Dublin, Ireland -
Full Time


Start Date

Immediate

Expiry Date

18 Oct, 25

Salary

0.0

Posted On

19 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

UNIPHAR – WHO WE ARE

With a workforce of more than 3000 employees spread across Ireland, United Kingdom, Mainland Europe, MENA, and the USA, Uniphar is a trusted global partner to pharma and MedTech manufacturers, working to improve patient access to medicines around the world. Uniphar provides outsourced and specialised services to its clients, leveraging the strong relationships with 200+ of the world’s best known pharmaco-medical manufacturers across multiple geographies, enabled by our cutting-edge digital technology and our highly expert teams. Uniphar is organised into three key divisions: Supply Chain Retail & On Demand, Uniphar Med Tech and Uniphar Pharma.

Responsibilities

THE ROLE

To support the Pharmasource/Ostomysource business units with the administration workload required for project dawn and for EWM/ S4 implementation in depots and G1.

MAIN DUTIES & RESPONSIBILITIES

  • Inspection of Exempt Medicinal Products upon receipt into the warehouse to ensure compliance with quality standards and regulations
  • Develop, update, and maintain quality processes and associated documentation in alignment with regulatory and business unit processes.
  • Coordinate and ensure completion of training programs for both new hires and existing staff
  • Responsible for the qualification and ongoing assessment of suppliers
  • Manage and update Quality Technical Agreements with relevant suppliers and vendors.
  • New product assessment and approval
  • Participate in cross-functional projects and undertake additional duties as assigned by the Quality Manager.
  • Oversee the management and resolution of EMP product quality complaints and adverse event reports in accordance with internal procedures and regulatory requirements
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