External QA Manager
Job Type | RemoteContractor |
Area | Dublin, Ireland |
Sector | Quality |
Start Date | |
Advertiser | Ashling Guthrie |
Job Ref | 3611 |
Job Views | 360 |
- 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