Ireland

Quality Specialist DRP, Old Connaught

Quality Specialist DRP, Old Connaught
Description
Position:

Quality Specialist&Deputy Responsible Person (dRP) Reporting to:

Quality Manager Contract:

Permanent, Full-Time Location:

Site-Based– Dublin or Offaly

Role Overview This position is responsible for providing quality oversight of product distribution within the supply chain. The role ensures that all product shipments are managed in compliance with Good Distribution Practice (GDP) requirements and applicable internal procedures.

The successful candidate will support Logistics, Customer Service, and Commercial functions while maintaining the highest standards of quality and regulatory compliance.

Experience&Qualifications

Minimum 5+ years’ QA experience in an HPRA/EU GDP-regulated environment

Strong knowledge of temperature-controlled distribution activities

In-depth understanding of Good Distribution Practice and global regulatory requirements for medicinal product wholesaling

Good understanding of pharmaceutical Wholesale Distribution Authorisation (WDA) business models, particularly quality and regulatory aspects

Excellent interpersonal skills with the ability to work effectively across a matrix organisation

Strong verbal and written communication skills, with the ability to present to different audience levels

Previous experience within a pharmaceutical wholesaler environment (preferred)

Experience with medical devices (desirable but not essential)

Key Responsibilities

Support the development, implementation, and maintenance of the Quality Management System (QMS)

Ensure compliance with GDP (2013/C 343/01) and HPRA guidelines (IA-G0046) across all activities

Promote quality awareness through training, retraining, and effective communication

Ensure all employees receive appropriate onboarding and ongoing GDP training

Verify that products are sourced from approved suppliers and distributed to approved customers in line with the Wholesale Distribution Authorisation

Assist in the qualification and approval of outsourced service providers and transport routes

Prepare, review, and implement quality documentation (e.g. deviations, change controls, validations, SOPs)

Perform initial and ongoing Bona Fide checks on suppliers and customers

Support a company-wide risk management culture

Maintain and review Quality Technical Agreements with relevant stakeholders

Manage product returns in compliance with GDP requirements, ensuring appropriate segregation and RP approval

Assess temperature-controlled shipments and make quality decisions on product disposition

Monitor temperature-controlled activities, including warehouse conditions

Escalate adverse reactions, product quality defects, or falsified medicines in line with regulatory requirements

Coordinate and manage product recalls in a compliant and timely manner

Act as Deputy Responsible Person (dRP), fulfilling RP duties in their absence and ensuring proper handover processes

Maintain accurate and compliant quality records across all systems

Ensure supply continuity while prioritising product quality and patient safety

Support additional duties and projects as assigned by the Quality Manager and Responsible Person

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