PROJECT LEADER JUNIOR MR

Job description

ROYAUME-UNI(Elstree)
du01 février 2020au01 février 2021(pour12mois)
ETABLISSEMENT :BAXTER SAS
REMUNERATION MENSUELLE :1840€ (indemnité non contractuelle fixée par décret et arrêté, dont le montant peut varier notamment en
fonction de l’évolution du barème de référence, de la localisation de la mission et des cas d’abattements prévus par les textes)

Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide.

Role and responsibilities:

The Project Leader leads project teams to project closure with limited direction. There is a level of independent interaction, influence, and leadership with the project team to ensure the team keeps the project on track and delivers to commitments. The Project Leader role is guided by the product lifecycle management processes. The individual in this role will be strengthening their independence and strong leadership and project management skills in order to evolve to leading larger projects.

Essential duties:

- Assign and track team deliverables for project completion Responsible for project communication by interacting with PMO Leadership, Project Core Team and extended teams to ensure effective communications and manage expectations
- Work within the guidelines of the organization's project office model, standard performance metrics, and regulatory guidelines to support, plan, monitor, control, and implement projects
- Coordinate project documentation
- Create and maintain project schedules In conjunction with the core team, establish, track and communicate project risks
- Maintain project team SharePoint Site In conjunction with the core team, establish and monitor project budget commitments, including purchasing of supplies and equipment as needed
- Understand and generate capital requests as needed

Support activities required in the design and development assurance for medical devices under the new European Medical Device Regulation (MDR).
Generate and manage work flow for appropriate change control documentation.
Provide technical input to projects and generate necessary protocols and reports.
Support the PDO in gathering information from Subject Matter Experts (SMEs) and technical resources for complaint investigations, change control, and regulatory submissions
Other tasks as needed.

Profile:

- Scientific or Technical/Engineering Master's Degree or equivalent and a first experience in project management
- Strong leadership potential
- Understanding of Good Manufacturing Practices, Good Laboratory Practices and Product Development Process requirements
- Proficient with scheduling software
- Product Development experience, familiarity with PMBOK is an asset
- Fluent in English