Senior Supplier Quality Expert

About Us:

How many companies can say they've been in business for over 177 years?!

Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the ever changing environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology.

We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team!

The Senior Supplier Quality Expert ensures the quality, compliance, and regulatory adherence of Eye Care products and nutritional supplements distributed and wholesaled by Zeiss Vision Care
. This position manages strategic relationships with contract manufacturers and wholesale partners, maintaining high standards of reliability, transparency, and quality. The role serves as the principal quality and compliance gatekeeper, with independent decision-making authority over supplier qualification, audits, regulatory readiness, storage/distribution, and recall management.

• Lead quality governance for distribution and wholesale, ensuring compliance with EU GMP, 21 CFR 210/211/820/111, ISO 13485, EU MDR, NMPA/SAMR, EFSA, DSHEA, ICH, and other standards.

• Establish and manage Quality Agreements, Technical Quality Standards, and audit frameworks with CDMOs and wholesale partners.

• Evaluate, qualify, and continuously monitor contract manufacturers and wholesale partners using a risk-based approach.

• Supervise GMP, GDP, and ISO 13485 audit programs, manage CAPA lifecycle, and ensure inspection readiness.

• Oversee packaging, labeling, and new product launches to ensure regulatory compliance.

• Develop and implement recall governance processes; coordinate recalls with partners, regulatory authorities, and internal stakeholders.

• Manage Nutrivigilance, safety assessment, and monitoring of dietary supplements.

• Support regulatory inspections and contribute to client and authority audits as a subject matter expert.

• Oversee end-to-end distribution operations including warehousing, shipping, receiving, inventory control, and order fulfillment in DACH countries, Belgium, and France.

• Ensure compliance with GDP, FDA, ISO, WHO, ICH, and other applicable standards.

• Manage relationships with external partners (freight carriers, warehouse providers) and implement KPIs to monitor performance, delivery accuracy, and inventory integrity.

• Ensure training and safety of warehouse staff.

• Drive continuous process improvement and digitalization within the distribution and wholesale Quality Management System to enhance compliance, efficiency, and transparency.

• Mentor internal quality professionals and implement training programs to elevate technical competence and inspection readiness.

• Lead cross-functional teams to manage the selection, contracting, onboarding, and day-to-day operations of CDMOs.

• Contribute to CMC due diligence for new collaboration partners, including quality, regulatory compliance, production capacity, and technological capabilities.

• Support negotiations of collaboration and technical agreements with partners.

• Establish and maintain strong relationships with CDMOs and collaboration partners to ensure long‑term operational excellence.

• Act as the key interface between internal functions (Regulatory Affairs, Supply Chain, R&D) and client representatives.

• Align with client quality teams on quality systems, performance KPIs, and strategic objectives.

• Bachelor's degree in Pharmacy, Chemistry, Biotechnology, Engineering, or related scientific field (Master's preferred).

• Advanced certification in GMP, GDP, or ISO 13485 Quality Management preferred (e.g., ASQ, EOQ, or equivalent).

• 5+ years' experience in international quality assurance within pharmaceutical, medical device, or distribution organizations (10+ years preferred).

• Demonstrated success managing complex distribution and wholesale networks and client partnerships in regulated global markets.

• Expertise in supplier qualification, change control, technology transfer, regulatory inspection management, and CMC development
  .

• Proven experience working with CDMOs and collaboration partners
  , including managing external alliances or technical agreements.

• Deep knowledge of GMP, GDP, ISO 13485, ISO 9001, ICH Q-series standards
  , and global regulatory requirements; ability to translate regulations into practical, operational processes.

• Strong leadership presence, strategic judgment, and integrity
  , with the ability to operate under…