Sr Qa Release Responsible Npi

Johnson & Johnson Johnson & Johnson · Pharma · Geel, Antwerp, Belgium +1

This role is a Sr QA Release Responsible for New Product Introduction in the pharmaceutical industry. The primary focus is on quality oversight of API product portfolios during the development phase, ensuring compliance with GMP and regulatory standards. Responsibilities include managing quality milestones, reviewing GMP documentation, investigating deviations and complaints, and acting as a spokesperson during health authority inspections. The role requires a strong understanding of cGMP, ICH guidelines, and Quality Systems, with experience in chemical and pharmaceutical supply chain or QA.

What you'd actually do

  1. Act as Quality Point of Contact for the Chemical Pilot Plants and for the release of an assigned API product portfolio.
  2. Assure Quality milestones and stage gate deliverables are achieved within the project timelines, including timely release.
  3. Support the quality oversight process of the operational activities by ensuring QA review and approval of GMP documentation.
  4. Ensure that deviations, CAPAs, Change Controls and Product Quality Complaints are timely and properly investigated by providing quality, compliance and technical expertise such that the internal and external customer expectations are met.
  5. Ensure that deviations and complaints with potential impact on patient safety and/or product supply are properly escalated.

Skills

Required

  • Master Scientific degree (chemistry, pharmaceutical sciences, bioengineer, microbiology…)
  • At least 5 years’ experience in Chemical and/or Pharmaceutical Supply Chain and/or Quality Assurance.
  • In-depth knowledge in cGMP (domestic & international), ICH guidelines, policies, standards and procedures.
  • Experience with Quality Systems.
  • Experience with regulatory inspections and preparedness.
  • Project management skills

Nice to have

  • Industrial Pharmacist – EU certified Qualified Person is an asset.
  • Experience within sterile/aseptic/low bioburden manufacturing is an asset.
  • Ability to quickly assimilate new modalities and technologies.
  • Demonstrated ability to work independently while staying connected with key stakeholders.
  • Strong analytical thinking skills, solution oriented thinking and able to work in a flexible way under time pressure.
  • Ability to make risk based decision under time pressure.
  • Understands the business implications regarding quality positions and decisions.
  • Demonstrated ability to work across organizational boundaries through influencing, negotiation and partnering.
  • Negotiation, communication and presentation skills across all levels of the organization are important.

What the JD emphasized

  • Phase Appropriate GMP Quality System
  • cGMP (domestic & international)
  • ICH guidelines