Project Manager - Supply Chain

Keyrus Life Science

To support the design and implementation of systems and processes within the TRD M&CS organization. This includes continuous improvement of the supply processes, systems and facilities.

The scope of this function includes supporting DS and DP Manufacturing as well as Clinical Supply organization, as from development through technical transfer to GIO across all systems, as needed

Job Description

  • Distribution SME, involved in the distribution strategy and business oversight of material transfers (imports and exports) of incoming material, intermediary product, and final product from/to TRD M&CS Warehouses to/from CMOs and other GSK sites.
  • Interact with external (CMOs, carriers…) and internal stakeholders (within R&D, GIO and Pharma) to define appropriate supply strategies and continuously improving them.
  • Prioritise and coordinate the distribution activities within TRD M&CS, among external and internal employees, follow-up and resolution of blocking points and appropriate escalation.
  • Lead and/or support key supply projects within the TRD GMP M&CS, as assigned; this includes all prioritized projects, such as strategic needs and facility improvements.
  • Manage the KPI supply strategy for TRD M&CS
  • Support warehousing and clinical supply activities through documentation revising, authoring; change control generation/closure; SOP/WKI updates/generation; etc. to ensure the success introduction of new/improved strategies. Support the risk management process and own remediation plans.

Profile

  • University degree in Logistics, project management or other relevant discipline
  • Project Management (pharmaceutical experience), GDP/Quality/ GMP, Biological product manufacturing, Business/Finance
  • Minimum of 5 years’ experience in Logistics Flow Management and very good knowledge of the GDP.
  • Project management experience within the pharmaceutical industry.
  • GMP knowledge across all development stages (Phase I – III).
  • Direct experience with KPI development/implementation, Operational Excellence, and/or continuous improvement.
  • Equally important is the ability to translate compliance and quality needs into successful support systems to ensure robust supply processes and facilities
  • Change Management experience ( Six Sigma experience is desirable)
  • French speaker and very good knowledge in English
  • Certified Project Manager credentials are desirable (or extensive project management experience)

What we offer

At Keyrus, thanks to the expertise of our people and external partners, each employee is welcomed with a varied integration program. You will join a dynamic and international environment with enthusiastic and professional colleagues.

We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.

Who we are

Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.

At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better

From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.

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