External QA Manager

https://www.teamhorizon.ie/job-search/1572-external-qa-manager/quality/dublin/job2025-05-13 15:23:332052-09-26Team Horizon
Job TypeRemoteContractor
AreaDublin, IrelandDublinIreland
SectorQuality
Start Date
AdvertiserAshling Guthrie
Job Ref3611
Job Views360
Description

Team Horizon is seeking an External QA Manager on a primarily remote basis. In this role you will have Quality and Compliance Oversight of CMOs.


 


 


Why you should apply:



  • This is an excellent opportunity to join a fast paced and diverse team, in a company who are committed to  discovering, developing, & manufacturing innovative human therapeutics

  • Opportunity to leverage your strong quality mindset across deviation management, reg affairs, filings, regulatory guidance in an external manufacturing role

  • Flexibility to work remotely


 


What you will be doing:



  • Quality and Compliance Oversight of a contract lab, CMO or a raw material SRE. Alignment with CTA / Marketing Application.
    Key Responsibilities

  • Be an integral quality member of cross-functional contract manufacturing team that includes but is not limited to business operations, analytical science, process development, supply chain XPD etc.

  • Negotiator and Approver of quality agreements

  • Lead the preparation of the site and represent company at product-specific Regulatory Inspections and/or during Notified Body audits of CM Site, as applicable or required.

  • Present on topics during inspection demonstrating appropriate behaviors and knowledge of the subject areas

  • Review / Approve Master Batch Records

  • Quality approver for deviations, change controls, CAPA

  • Prepare inspection playbooks

  • Identify and mitigate Risk at the CMO or testing Laboratories and/or escalate to management

  • Perform Person in Plant activities as required

  • APR Data Provider

  • Manage Audit commitments to completion

  • Perform tactical batch disposition activities in support of lot release

  • Release or Reject batches/ Approve or reject deviations, Change Control, CAPA

  • Provide Quality position on GMP related topics and strategy for the site

  • Decision to approve Master batch Records/Raw Material Specifications


 


What you need to apply:



  • 10 + years biotech or pharmaceutical industry experience

  • Significant Quality experience at Aseptic Manufacturing facilities

  • Able to facilitate and influence senior stakeholders and partners

  • Able to successfully manage workload and timelines

  • Familiarity with basic project management tools

  • Ability to negotiate a strategic position after taking feedback from multiple sources

  • Strong project management, problem-solving, and analytical skills

  • Demonstrated ability to lead cross-functional teams, consistently deliver on-time, and high-quality results

  • Collaborates and communicates well with others, able to balance divergent inputs from various stakeholders and drive issue resolution

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