Project Manager

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Risskov

The Project Manager is responsible for formulating, organising, co-ordinating and performance monitoring of site projects for the Operations functions of LGC Genomics.

The position directs and controls the associated project team resources ensuring plan deviations are identified and corrected to deliver the project key objectives and is responsible for the implementation of governance processes and tools application to ensure consistent reporting delivery to the VP Operations.

The Project Manager reports to the Global Program Manager as part of a team of project managers located across LGC sites in EMEA and NA.

Key Responsibilities:

  • Creation of detailed Project Plans, engagement of key stakeholders to approve project deliverables.
  • Co-ordinate internal and third party resources to achieve project deliverables (scope, time, budget).
  • Measure performance utilising appropriate tools and techniques.
  • Preparation of material for Investment cases for Board approval.
  • Creation and maintain comprehensive project documentation for internal and external regulatory requirements.
  • Establish and maintain relationships with stakeholders at all levels of the organisation.
  • Continually develop skills and train other in the use of project tools and assist best in practice adoption.
  • Other duties, as assigned

Knowledge, Experience and Technical Skills:

  • Proven working experience in project management.
  • Suitable project management qualifications (PMP / Prince II)
  • Excellent written and communication skills with effective meeting and presentation skills.
  • Ability to gather and organize information, Interpret and develop appropriate recommendations for senior leadership.
  • Experience working with a wide range of people and functions across geographically diverse locations.
  • Strong analytical, problem-solving, time-management and organizational skills.
  • Passion for continuous improvement with demonstrated initiative.
  • Goal and team oriented individual
  • English language required.

Education and/or Experience:

  • Significant experience leading project activities in dynamic, fast changing and highly regulated industries.
  • Experience of operating with FDA / MHRA regulatory environments in IVD supply chain.
  • Demonstrative experience of leading and successfully delivering large, complex projects with significant business improvements.

Physical Demands:

  • Requires prolonged sitting and working at a computer monitor. Repetitive motion using a keyboard for long periods of time. May occasionally be required to lift and move material weighing up to 50 lbs.

Work Environment:

  • Site based.

How to apply?

Please click at the box "SØG JOBBET" and upload resume and CV in English.

Kilde: Jobnet.dk


Information og data

Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".

Arbejdsstedet er beliggende i Risskov.

Jobbet er oprettet på vores service den 13.3.2021, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Projektleder
  • Risskov
  • Fredag den 26. marts 2021

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