Site Quality Head, Geel

Johnson & Johnson Johnson & Johnson · Pharma · Geel, Antwerp, Belgium

This role is for a Site Quality Head at Johnson & Johnson in Geel, Belgium. The position involves leading and managing all quality-related programs and activities for manufacturing operations, ensuring compliance with cGMP, regulatory policies, and guidelines. The Head will oversee Quality Control, Quality Assurance, Quality Systems, Compliance, and Product Release, and will be a key member of the site leadership team, partnering with global quality teams and regulatory bodies.

What you'd actually do

  1. Overall Quality responsible for the Janssen Chemical site in Geel, is accountable for cGMP and the Quality Operations for the chemical operations in Geel for both manufacture of commercial and clinical API’s and drug product intermediates (spray drying).
  2. Provide overall leadership and direction to the quality organization, building processes to improve the capabilities of the organization.
  3. Assures appropriate processes and resources are in place and effective to deliver a sound compliance profile in the Geel site.
  4. Actively participates as a member of the Geel Site Leadership team and partners with the Site General Manager.
  5. Serves as a member of the SM Quality Leadership team, to develop common quality strategies across the API sites and the Small Molecule (SM) platform, benchmark best practices internal and external to J&J, work with Compliance team to develop global Quality policies for API SM, assure implementation of these policies and serve as a sponsor to selected processes.

Skills

Required

  • B.S. in a scientific/technical discipline with 11–15 years’ experience in a significant leadership position within the chemical and/or pharmaceutical industry, or Master’s Degree in scientific/technical discipline with 10+ years above experience.
  • 5 years’ experience in a Quality leadership role.
  • Knowledgeable of FDA/EMA regulatory requirements applicable to chemicals or pharmaceuticals.
  • Thorough knowledge of GMPs is required.
  • Ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position.
  • Excellent written and verbal communication skills with an open, collaborative, interactive leadership style.
  • Balanced decision-maker.
  • High-energy level with a commitment towards achieving results with strong follow-through.
  • Ability to build and nurture strong and positive relationships.
  • Demonstrated strategic thinking capabilities and the ability to help define a vision for the future.
  • Team collaboration and coaching skills.
  • Ability to work in a team environment and interact with all levels of the organization.
  • Results-driven leader who commits to stretch goals and delivers results.

Nice to have

  • Significant experience in supporting functional area (e.g., R&D, Manufacturing, Engineering, EH&S, Tech Services) preferred.

What the JD emphasized

  • cGMP
  • FDA/EMA regulatory requirements