Consultant Technology Management Drug Product (m/w/d)

Job Details

Zusammenfassung

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Job Details

Ihre Aufgaben

  • As a Freelance Consultant, you will serve as the central technical expert for all aspects of technology management in the Drug Product (Solid Dosage Forms) area. You will take on a key role in ensuring compliance and the successful market launch of p
  • Site Launch & Tech Transfer: Advise and guide teams for all Site-Launch activities (incl. lab units, SC, RACMC, and QA). This involves communicating and coordinating with internal and external sites.
  • Technical Documentation & Compliance: Expert review and approval of technical documentation (protocols, reports) associated with manufacturing, tech transfer, site-to-site transfers, and Process Performance Qualification (PPQ).
  • Strategic Manufacturing Planning: Communicate and implement manufacturing plans at the site which are aligned with cross-functional CMC strategic discussions.
  • Data Liaison and Analysis: Conduct data review and analysis, support the data-driven decision-making process, and act as the liaison between the Tech Strategy (data digitalization) team and the site to support data transfer.
  • Regulatory Consulting: Advise on the compilation and technical review of relevant CMC sections of regulatory submissions (NDAs, BLAs, etc.), responses to regulatory questions, and briefing books.
  • Risk Mitigation: Recommend remediations and CAPAs and provide inspection support as appropriate to mitigate risks or gaps.
  • Project Participation: Participate in CMC working group meetings and communicate clear, timely, and detailed updates on tech transfers and site activities to stakeholders.

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Michaela Burkhardt

Michaela Burkhardt

Teammanager Sales

Willkommen bei Randstad! Ich bin Ihr persönlicher Ansprechpartner und berate Sie gerne zur ausgeschriebenen Position und zu Ihren Karrieremöglichkeiten.

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