External Supply QA Manager at Amgen
Dún Laoghaire, County Dublin, Ireland -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

0.0

Posted On

09 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Pharmaceutical Industry, Manufacturing Processes, Timelines

Industry

Pharmaceuticals

Description

DESCRIPTION

Quality and Compliance Oversight CMOs and alignment with CTA / Marketing Application.

Responsibilities
  • Be an integral quality member of Amgen cross-functional contract manufacturing team that includes but is not limited to business operations, analytical science, process development, supply chain, etc.
  • Lead the representation, communication and management of quality issues with internal partners and external partners
  • Serve as the main Quality point of contact and approver for deviations, change controls, CAPAs, and batch disposition etc. related to Amgen product.
  • Manage CMOs to contractual obligations relative to Quality Agreement, Amgen specifications, quality, safety and regulatory requirements.
  • Review completed production batch records as necessary and approve master batch records, and other cGMP documents from CMOs / Contract Laboratories.
  • Provide quality oversight of the manufacturing, testing, and release of Amgen products at CMOs.
  • QA review of all documentation associated with batch release to ensure GMP compliance.
  • Negotiator, author and Approver of quality agreements
  • Lead the preparation of the site for and Represent Amgen at product-specific Regulatory Inspections and/or during Notified Body audits of CMO Site, as applicable or required.
  • Contribute to the successful outcome of all regulatory inspections associated with company business, both internally and at contract manufacturers as required. Present on topics during inspection demonstrating appropriate behaviors and knowledge of the subject areas
  • Review / Approve Master Batch Records
  • 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
  • Provide Amgen Quality support of CMO site activities (e.g., NPI, tech transfer, PPQ, filings, etc.) site in accordance with the Quality Agreement
  • Monitor and communicate site performances in means of quality metrics to Amgen and Contract Manufacturer
  • Identify prioritization opportunities and determine when escalation is necessary
  • Develop strong partnership/relationship with CMO / testing Lab
  • Manage submission related activities at CMOs as it pertains to international launches, global expansion etc.
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