Project Manager MS&T
Teva Pharmaceutical
Haarlem, NL, 2031
3 dagen geleden

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.

Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day.

We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.

This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth! Job Description

Within the MS&T (Manufacturing Science and Technology) department we are looking for a Technical Project Manager.

You will be responsible for managing multiple projects, planning, implementing and concluding projects on new (and increasingly complex) sterile products and manufacturing processes.

These projects from the R&D Teva sites (Technology Transfer) will be made operational in the cGMP plant. You will lead the project team and interact with all departments within the organization, as well as Teva sites outside the Netherlands.

You will be an expert in a specified technical area of sterile / cGMP manufacturing process(es), and provide technical support to the project 2 years post commercialization.

Responsibilities include :

Responsible for all aspects of project management, such as listed below

  • Supervise introduction of new processes and improvement of existing ones
  • Develop project plans, assemble and lead multiple project teams
  • Manage project budgets, timelines and deliverables
  • Lead project team and other relevant meetings, coaching team members
  • Present project status to stakeholders and (senior) management
  • Determine priorities within own project, while keeping track of project execution across multiple departments
  • Be the face of your projects within Teva
  • Drive process improvement and operational excellence initiatives
  • Serve as the expert on a specific project and / or technology, consult with internal / external experts on technical matters, such as listed below :

  • Participate in the design phase of manufacturing processes to ensure smooth transfer to operations, and taking a leading part in their implementation in production.
  • Develop new technical procedures and guidelines,
  • Write manufacturing instructions, product specification files, reports
  • Fulfill the role of a Subject Matter Expert
  • Qualifications

  • At least 3 years experience in the pharmaceutical industry, preferably in a sterile GMP environment of a multinational company
  • MSc (PhD preferred) in Life sciences, bioprocess engineering / technology, pharmacy, chemistry or similar
  • Experience with project management
  • Experience with line management
  • Team player with sound communication skills and pro-active approach.
  • Experience with developing and / or manufacturing complex sterile products (freeze drying and advanced drug delivery systems) is an advantage
  • This is a multifaceted challenging position with possibilities for visibility and growth within our company.
  • Function Research & Development Sub Function Drug Analysis and Formulation Reports To In process of validation

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