Investigational Product Delivery Lead für Experis in Kaiseraugst - myjob.ch
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      11.06.2026

      Investigational Product Delivery Lead

      • Kaiseraugst
      • Festanstellung 100%

      • Merken
      • drucken
       

      Experis

      Experis

      Investigational Product Delivery Lead


      We are looking for an Investigational Product Delivery Lead for one of our main clients in Kaiseraugst.

      Description: Key Responsibilities (6-8 bullet points):

      • Coordinate end‑to‑end investigational product delivery across 5–10 active clinical trials
      • Act as the single coordination point between various stakeholders, Clinical Trials Management, Clinical Operations, technical teams, Quality, Manufacturing, Supply Chain, Analytics, and external partners
      • Actively engage and follow up with functions to ensure execution against timelines, quality, and regulatory requirements
      • Maintain constant, structured communication with technical teams to translate clinical needs into executable technical actions, and keep all functions involved well informed and aware about changes in timelines
      • Ensure consistent application of the IP process with focus on:
        • Robustness
        • Adherence to approved processes
        • Traceability and documentation
        • Continuous improvement
      • Proactively identify risks, gaps, and dependencies and drive resolution through direct outreach
      • Support governance through clear reporting, visibility, and portfolio‑level tracking
      • Lead and facilitate monthly cross‑functional IP coordination meetings and contribute to portfolio reviews


      You bring (6-8 bullet points):
      ·

      • Degree in Pharmacy, Pharmaceutical Sciences, Chemical Engineering, Materials Science, Chemistry, or a related scientific discipline.

      • Good understanding on dietary supplement product development and manufacturing procedure from idea to product

      • 3–5 years hands‑on experience in:

        • Quality and/or Pharmaceutical Technology
        • Oral Solid Dosage Forms
        • Relevant regulatory frameworks (e.g. Pharmacopeia, GMP)
        • Dietary supplement experience
      • Solid understanding of clinical trial workflows

      • Experience with CTMS, Veeva, or equivalent clinical systems

      • Basic but practical project management capability

      • A strong understanding of materials and chemical sciences is considered an asset.

      • Process deployment, execution monitoring, and reporting

      Contact: alba Jansa: alba.jansa@experis.ch

      Arbeitsort: Kaiseraugst