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AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Principal Clinical Supplies Project Manager (all genders) - (temporary 24 months / fulltime)

Ludwigshafen am Rhein, Rhineland-Palatinate, Germany Req ID 2211005 Category Research and Development Division AbbVie
  • Provide project coordination/management & logistical support for multiple global project teams (agenda, minutes, action item follow up). Schedules and leads cross functional team meetings with both internal and external partners.
  • Provides relationship management in conjunction with project coordinator at CRO and/or external collaborator sites. Identifies and resolves bottlenecks and team dynamic concerns.
  • Ensure effective, accurate and timely communication of critical information to internal and external project team members.
  • Ability to interact with higher level personnel (Director Level and above) across development teams including personnel from development, formulations, quality, analytical and regulatory.
  • Collaborates with formulators and process engineering on process development and bringing new products into the pilot plant. Has an understanding of both product development and manufacturing and can identify transitional challenges between the two.
  • Provides technical feedback to the project team. Provides leadership using troubleshooting skills and identifies solutions to issues that arise during manufacturing or packaging.
  • Leads scheduling and supply chain activities with multiple global partners and sites. Leads the resolution of schedule conflicts. Manages manufacturing prep activities including materials management to enable manufacturing to start on time.
  • Ability to lead clinical manufacturing projects with extremely complex supply chains emphasizing external interaction especially with cross-cultural teams across multiple global sites (Ludwigshafen, Puerto Rico, Sligo, Cork and TPMs) in the context of managing logistics for an internal/external project and/or functional area initiative. Internal logistical support of internal project leader and core team.

  • Bachelor's degree. in Chemistry, Biology or related scientific area or equivalent and relative work experience.
  • Minimum of 10 years of experience in Operations, R&D, supply chain management, and/or related area.
  • Experience in a cGMP environment is highly desired. 
  • Analytical and communication skills
  • Excellent command in English language

Travel: No
Job Type: Experienced
Schedule: Full-time
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