Quality Control Lead

3 tygodni temu


Wrocław, Województwo dolnośląskie, Polska TN Poland Pełny etat

About this opportunity

The Quality Control Lead manages the department resources in order to ensure that the devices are manufactured and distributed to the customers according to the specifications and is responsible for managing the team of Quality Control Supervisors. The Quality Control Lead provides coordination of Quality Control expertise on daily production issues, process improvements, guidance on failure analysis and customer complaint resolution, and interfacing with outside regulatory agencies.

In this role, you will:

  1. Identify and manage projects to improve the effectiveness of the Quality Control area.
  2. Implement and maintain standardized local QC KPI's, aligned with global KPI's, and implement and maintain systems to archive these and make these easily retrievable.
  3. Report out on these KPI's.
  4. Ensure the effective fulfillment of objectives and deadlines assigned to the group, including managing product inspection and release activities directly or through the team, quality criteria application, and timely relevant QC data reporting.
  5. Lead and coordinate all the preparation and hosting activities related to any corporate or outside agency inspections towards QMS in the Quality Control area.
  6. Oversee identifying issues within the quality control area that need correction, preventive and corrective action.

In this role, you'll need:

  1. Minimum 5 years experience working in Medical Device, Pharma, or life science Quality Management position is required.
  2. Experience in Quality Control development and implementation within the Medical Device Industry.
  3. Fluent English and Polish required (reading, writing, and conversation).
  4. Strong written and oral communication abilities required and the ability to synthesize information to present as requested.
  5. Exceptional interpersonal skills and the ability to work cross-functionally.
  6. Exclusive level of commitment and a positive can-do attitude.
  7. Must be able to work independently as well as in close collaboration with others.
  8. Ability to do research and come up with creative, compliant solutions for QC/QMS challenges.
  9. Demonstrate leadership, attention to detail and ability to solve problems and communicate issues; ability to work on multiple projects.
  10. Experience in the creation and follow-up of Corrective and Preventive actions.

Work environment demands:

  1. Strong interpersonal communication skills with the ability to build relationships.
  2. Open-minded, stress-resistant person with the ability to work in interdisciplinary teams.
  3. Independence and ability to work under time pressure.
  4. High level of interpersonal skills.
  5. Ability to focus attention to details.
  6. Ability to consistently follow through with projects to completion.
  7. Capable of working in a fast-changing environment.

We offer:

  1. Medical care in Luxmed.
  2. Multisport programme.
  3. Attractive group insurance (PZU or UNUM).
  4. Employee discount programme for company products (Invisalign).
  5. Co-financing of meals in the company canteen.
  6. Co-financing from the Company Social Benefits Fund.
  7. Opportunities for professional development.
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