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Quality Manager within IMP Quality Clinical Packaging

Engineering
Basel
English


The roles within IMP Quality Operations Switzerland Clinical Packaging Team require a high level of flexibility, ability to work under pressure and sense of responsibility.
You are inspiring, self-reflected and creative on the one hand and are clear in communication as well as integrative in solution processes on the other. 

General Information:

  • Start date: asap
  • Latest Start Date: Hiring manager considers candidates with a notice period of max. 3 months
  • End date: 1 year
  • Extension: possible
  • Workload: 80-100%
  • Home Office: Min. 60% onsite
  • Team: 12 team member


Tasks & Responsibilities:

  • Support all quality-relevant packaging processes and collaborate with packaging operations and all relevant interfaces with regard to GMP topics
  • Partner with stakeholders and provide GMP support to ensure successful delivery of the company goals
  • Review and release of manufacturing specifications and Batch Records (BR) of finished and semi-finished goods
  • Manage actively Deviations and Changes
  • Collaboration through to the management of local and global projects
  • Actively engage in optimization activities and improvements within IMP Quality Clinical Packaging Switzerland. Coordinate improvement projects and engage in corrective and preventive measures (CAPA)
  • Build, verify and implement standard documents (SOPs)
  • Joy in a human-centered and self-managed way of working based on NewWork, with a key focus to support the ongoing cultural and organizational change towards collaboration, agility and innovation mindset


Must Haves:

  • Master Degree preferably in Life Sciences or Engineering or similar degree
  • Min. 3 years of experience in the pharmaceutical industry in a quality manager role 
  • Experience in the area of pharmaceutical development such as packaging lines / materials, master data management, quality control or quality assurance is an advantage
  • Kledge of cGMP and quality requirements for clinical development phases
  • Proven track record to work towards outcomes and an innovative manner of solving problems 
  • Strong team-player with a high level of self-motivation and being able to inspire others
  • Ability to work in a purpose driven organization, taking full ownership for assigned roles and tasks, continuously willing to improve individual and team effectiveness
  • Ability to communicate clearly and professionally verbally and in writing in BOTH German and in English
  • Experience with SAP and Veeva is a plus


We thank you for your application ;)