Quality Specialist DRP, Old Connaught
Quality Specialist DRP, Old Connaught
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Old Connaught, Ireland
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Posted: less than a month ago
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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
#J-18808-Ljbffr
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
#J-18808-Ljbffr
Highlights
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Company nameForce
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Job positionQuality Specialist DRP
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