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Director of Quality
  • Siemianowice Śląskie
Director of Quality
Siemianowice Śląskie, Siemianowice Śląskie, Silesian Voivodeship, Polska
Phillips Medisize
22. 1. 2026
Informacje o stanowisku

Director of Quality at Phillips Medisize

Phillips-Medisize, a Molex Company, is seeking a Director of Quality to oversee the effective execution of quality systems, representing the business to align with global regulations and provide global leadership and direction to the sustaining Quality teams across Europe and Asia.

Phillips-Medisize, a Molex Company is an end‑to‑end provider of innovation, development, and manufacturing solutions to the pharmaceutical, diagnostics and medical device industries. The largest pharmaceutical, MedTech and in‑vitro diagnostic companies in the world count on Phillips‑Medisize to bring their breakthrough ideas and innovative branded products to market – with confidence. As a contract design and manufacturing organization (CDMO), we work closely with our customers to deliver proven, highly engineered products that help millions of people live healthier, more productive lives.

What You Will Do

  • Provide direction and leadership to the cross‑functional, multicultural Quality teams including people management in Ireland, Poland, Finland, China and Thailand.
  • Maintain and improve quality to support the Strategic Medical Plan for new business opportunities.
  • Cultivate and “audit ready” culture and ensure compliance with all medical device and pharmaceutical regulations and quality system requirements.
  • Work with Commercial team to represent Phillips‑Medisize Quality System with customers and potential customers.
  • Drive continuous improvement activities using tools like Six Sigma, MSA or other statistical methods.
  • Manage and improve Key Performance Indicators (KPIs).

Who You Are (Basic Qualifications)

  • B.S. degree in quality, business, engineering field or other technical field.
  • Ten years or more experience in a quality role.
  • Five years or more experience in a management role.
  • Strong preference for regional or multi‑site responsibilities.
  • Experience in Medical discipline/industry.
  • Knowledge of FDA and international regulations and ISO standards related to medical device design and manufacturing (e.g. MDR, 21 CFR 11, 820, 211 and ISO 13485, 14971).
  • Experience using quality tools, such as SPC, design of experiment (DOE), root cause analysis.
  • Direct experience with audits and pre‑approval inspections by regulatory authorities.

What Will Put You Ahead

  • Experience working with SAP systems.
  • Multilingual.

At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate’s knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.

Who We Are

Phillips Medisize, a Molex company, collaborates with industry leaders to design and manufacture drug delivery systems, medical devices and diagnostic tools that save and improve the quality of life for millions of patients annually. With our dedicated team of 6,000+ employees in 29 locations around the world, we share our customers’ mindset that every product is critical to a healthcare provider and their patients somewhere in the world. Molex is a multi‑sector global electronics brand owned by Koch, Inc., one of the world’s largest privately held companies. Discover your potential to make a difference.

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