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Drug Product (Project Manager)

RESPONSIBILITIES

Be accountable for the 7 pillars of PM:

  • Budget:Apply project cost policies, procedures & documentationControl cost at project level & report deviation
  • Timelines:Consolidate all project activities (incl. duration & sequence)Build project schedule & propose it as a baselineControl schedule at project level & report deviation
  • Documentation / Deliverables:Consolidate requirements (project scope)Consolidate Work Breakdown Structure at project levelControl scope at project level & report deviation
  • Communication / Reporting:Ensure that all departments and experts receive information needed to perform their tasks properlyBuild reporting for different levels of communication 
  • Monitoring:Project’s execution oversightProject’s progress review & regular updatesEndorsement of project deliverables
  • Risk Management:Apply project risks policies, procedures & documentationEnsure regular reporting on residual risk assessment 
  • Resources:Consolidate project resource needs from all departments and experts Control resource at project level & report deviation
  • Drug Product (DP)Effectively coordinate the implementation of an end-to-end Drug Product manufacturing facility (Formulation, Filling, Packaging, analytical, logistics, procurement...)Develop DP Feasibility and Design studies to support strategic decisions and technical investment projects in cooperation with partners
  • Relationship and coordination managementStimulate, align and coordinates all stakeholder’s contributions.Be the key interface with our client and partners.Act as facilitator to integrate all technical contributionsReport and escalate to management as needed.Successfully manage the relationship with the client and all stakeholders.
  • Quality, Compliance, EHS managementEnsure these requirements are always taken into account.Collaborate with the EHS, quality & compliance local officers.
  • Risk management & reportingImplement issues & risks management systems.Develop recommendations and action plans to resolve issues and mitigate risks, affecting or likely to affect the successful execution of the projects.
  • PROFILE (QUALIFICATIONS, SKILLS & EXPERIENCE)

  • Master’s degree in business and technical (bioengineering, biology, engineering…) fields.
  • 5 years of proven project/program management experience in an international environment ideally in a similar role within the (bio)pharmaceutical industry (vaccines, mAbs, …)
  • Exposure to sub-Saharan African markets is a clear asset
  • A project management certification (PMP, Prince 2, PM²) is a clear asset. 
  • A strong knowledge in GxP Drug Product manufacturing.
  • Self-motivated and passionate about the company’s mission to improve access to high-quality healthcare in emerging markets.
  • Ability to communicate in a practical and commercial manner at all levels.
  • Ability to collaborate with multiple cross disciplinary teams.
  • Ability to prioritize for delivering quality projects on budget and on schedule.
  • Stress resistant, agile and ability to deal with uncertainties specific to start-up companies/SMEs.
  • Autonomous, you are a problem-solver with the ability to see problems as challenges and life experiences and try to stand above them, objectively.
  • Fluent in English and French.
  • Anderen bekeken ook

    Drug Product (Project Manager)

    Bedrijf:
    Univercells
    Gemeente:
    Charleroi
    Contracttype: 
    Vast contract, Voltijds
    Categorieën: 
    Project Manager
    Opleidingsniveau: 
    Master
    Carriereniveau: 
    Manager
    Gepubliceerd:
    31.08.2022
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