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Project Manager for Medical Device Component Development

vor 2 Monaten


Ravensburg, Baden-Württemberg, Deutschland Vetter Pharma Vollzeit

Job Summary:

We are seeking a highly skilled Project Manager to lead the development and implementation of new primary packaging systems or components in collaboration with suppliers and external service providers. The successful candidate will be responsible for managing all cross-functional activities, ensuring the development of trays and their availability on all Vetter equipment, and creating required product documentation in accordance with CFR 820 and MDR.

Key Responsibilities:

  • Develop and implement new primary packaging systems or components in collaboration with suppliers and external service providers.
  • Manage all cross-functional activities, including the development of trays and their availability on all Vetter equipment.
  • Create required product documentation in accordance with CFR 820 and MDR.
  • Identify and evaluate new ideas for patent applications, conduct patent research, and assess external submissions.
  • Develop and organize the development of new test procedures/test methods in the project in close collaboration with other departments and in coordination with suppliers.
  • Analyze and evaluate internal requirements and ensure alignment with Vetter's process capabilities and those of suppliers, in collaboration with internal interfaces.
  • Plan, prepare, and conduct presentations and training sessions for employees of the operating organization and other involved departments, as well as communicate project topics to customers and suppliers.

Requirements:

  • Master's degree in a technical field (e.g., packaging technology, plastics technology, medical technology) or a comparable degree.
  • Expertise in the development of packaging systems and components, with several years of professional experience.
  • Several years of project management experience in a technical environment.
  • Knowledge of applicable regulations, particularly CFR 820 and MDR.
  • Knowledge of quality management and pharmaceutical validation procedures and methods.
  • Good IT skills (MS Office, MS Project, SAP).
  • Excellent English language skills, both written and spoken, due to Vetter's international business activities and the associated tasks.
  • Strong communication and team skills, as well as high social competence.
  • Ability to work independently and take responsibility, with a high level of reliability and diligence.

About Vetter:

  • Independent and interdisciplinary work in a family-owned company with modern working conditions and innovative technologies.
  • Strong team + career opportunities - idea exchange and many opportunities for further education at one of the leading pharmaceutical service providers.
  • Attractive remuneration - with bonuses for shift and overtime work, holiday pay, and a year-end bonus.
  • Good work-life balance - with at least 30 days of holiday, offers for combining family and work until the possibility of working partially remotely.
  • Vetter's pension plan - an ideal combination of age and health pension plans, e.g., company pension plan.
  • Occupational health management with fitness and sports offers (EGYM Wellpass).
  • Personal benefits (Germany ticket, Vetter holiday homes, JobRad, employee discounts, etc.).