Upstream Process Director m/f/d

      On behalf of our client Sandoz, a global leader in generics and biosimilars, we are looking for an experienced Upstream Process Director to join their biologics manufacturing leadership team in Lendava, Slovenia.

      Region
      Grad Zagreb
      Place of work
      Lendava
      Published on
      28. 7. 2025
      Deadline
      27. 8. 2025

      This is not just another management role — it is a foundational opportunity to build and shape an entirely new Upstream Production Unit at one of the largest biosimilar investments in Europe.

      You will be responsible for designing and operationalizing a highly specialized manufacturing system for cell-based biologics production – specifically working with cell cultures in aseptic conditions, from inoculum preparation through bioreactor-based protein synthesis.

      If you have a deep technical background in  the production of biosimilar or comparable biologic medicines, a passion for leading people, and the ability to set up operations at scale, this is your moment to make a lasting mark in the biosimilars world.

      We offer:

      • Employment at Slovenia’s most reputable employer
      • Permanent contract with a 6-month probation period
      • Competitive salary and annual bonus
      • Relocation support
      • Pension scheme and employee recognition programs
      • Health & well-being support via the “Energized for Life” initiative
      • Unlimited professional development and internal growth opportunities

      Main tasks:

      • Oversee biologics (biosimilar) upstream production processes, ensuring full compliance with GMP, HSE, and all relevant regulatory standards
      • Lead aseptic cell culture operations: inoculum preparation, media production, bioreactor-based protein synthesis
      • Prevent contamination through precise process control in a sterile environment (pH, temperature, oxygenation)
      • Manage manufacturing staff to ensure strict adherence to safety, quality, and hygiene protocols across 2-shift operations, 7 days per week
      • Design and implement new systems for safety, material flow, documentation, and training – entering at the project phase, not a completed setup
      • Collaborate cross-functionally with QA, QC, supply, downstream, and warehouse teams
      • Represent the unit during regulatory inspections and internal audits
      • Develop and oversee the budget for upstream operations
      • Integrate digital and smart manufacturing technologies to enable predictive maintenance, real-time quality control, and advanced traceability
      • Drive process optimization to enhance operational efficiency, reduce costs, and improve batch consistency
      • Promote green manufacturing practices, reduce waste, and support sustainable drug development
      • Recruit, onboard, and develop new team members
      • Translate organizational needs into training and development programs

      We expect:

      • Minimum 5 years of working experience (preferably in biologics production processes) and people management skills.
      • Technical background: degree in biotechnology, pharmacy, chemistry, or related field
      • Proven leadership and team development experience
      • Hands-on experience in biopharmaceutical production, preferably in upstream biologics, aseptic, or organic production environments
      • Fluent in English
      • High resilience, adaptability, and ability to maintain momentum in a dynamic project environment
      Apply now