Quality Supply Chain Manager

  • Location

    Frankfurt (Oder)

  • Sector:

    Quality

  • Salary:

    65,000EUR - 77,000EUR

  • Contact:

    Rebecca Stevens

  • Job ref:

    22914

Quality Supply Chain Manager

Based in Hessen (hybrid)

Our client is a global leader (top 10 worldwide) of active medical devices at Class III and pharmaceutical drugs. They are in the middle of a global project across 54 sites in EMEA, Latin America and Asia Pacific to reduce complexity in business processes for the QM department by designing new interfaces and sub-systems for all areas of quality - design control, CAPA, Supplier Management, PMS.

As the Quality Supply Chain Manager (m/f/d), it is your responsibility to guarantee that all regulations, health and safety standards, and conformity criteria are followed, as well as that the wholesale business complies with GDP (good distribution practises).

 

Your Responsibilities

  • You introduce and maintain the quality management system.
  • You (further) develop the GDP process and SOP landscape.
  • You implement appropriate facilities and processes for optimal storage and maintenance of products.
  • You will ensure operational wholesale operations in compliance with specific national specifications and qualification requirements.
  • You assist in the coordination and execution of processes to handle returned, rejected, recalled or counterfeit products.
  • You support in communicating with/to authorities (e.g. RP Darmstadt, TÜV SÜD)
  • You create training programs for training and qualification of employees

 

Job Requirements

  • You have a completed bachelor's degree, ideally a higher degree.
  • You have several years of practical experience in the field of distribution of medical devices and pharmaceuticals.
  • You have experience in a similar position with expertise as a person responsible for wholesale trade according to GDP and AMG.
  • You understand the quality management system processes and their implementation in electronic quality management software solutions.
  • You are proficient in applying quality management standards (e.g. ISO13485) and medical device regulations and drug regulations (e.g. MDD/MDR, GMP, AMG, AMWHV Article 83 2001/83/EU, ICH Q10).
  • You have Extensive knowledge in SAP, TrackWise, PTC-Windchill or comparable.
  • You are collaborative with strong communication skills, ability to work in a team and are willing to travel!
  • You have a very good knowledge of German and English, both written and spoken

 

Your Benefits

  • You will work globally with over 10,000 employees and expand your international network!
  • You profit from 30 days of vacation
  • You can enjoy Flexible hours, continuous development, pension scheme and more.
  • Travel to different production sites and become and expert of the company’s presence in Germany

 

Are you interested to find out more about this role? Please contact Vera-Lucia Bösch for further details:

Email: vera-lucia.boesch@adaptivelifescience.com

Phone: +49 30 16 63 68 37

#LH-VB1 #remote #hybrid