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Director, Vaccine Technical Services/Manufacturing Science (TS/MS) (m/f/d)

Cuxhaven, Niedersachsen · Manufacturing
Our client is a world's leading animal health company with more than 5,800 employees worldwide. With over 65 years of tradition, they develop products and services to improve the health and well-being of pets and farm animals in over 90 countries.
For the category of vaccines for animals, in Cuxhaven or remotely (with ca. 3 days/week office presence) we are currently looking for a
Director, Vaccine Technical Services/Manufacturing Science (TS/MS) (m/f/d)
The Technical Director is an active member of the Cuxhaven Plant Leader Team and serves as the local advocate for the Corporate TS/MS.
Your responsibilities:
  • Lead the organization responsible for scientific and technical stewardship of vaccine
  • Lead the process monitoring strategy to ensure process capability is maintained processes
  • Process design, development, optimization, scale-up, technology transfer and validation of the product lifecycle from master seed to launch and post-launch product improvement
  • Coach, learn and perform problem-solving (scientific method) in order to develop employees
  • Ensure commercialisation of new products is timely, robust, registered appropriately and cost effective
  • Act as the local M&Q process owner for the local manufacturability review
  • Ensure technical transfers are delivered on time and with robust manufacturing control strategies implemented
  • Liaise effectively with donor sites
  • Cultivate a collaborative and effective continuous improvement culture across multiple functional areas including Production, Regulatory, QA, QC, Supply Chain, Engineering, Clinical, Analytical Development, R&D
Your profile:
  • Degree level or higher in Pharmacy, Biochemistry or (Bio) Chemical Engineering
  • Biotech manufacturing experience
  • Substantial experience in a variety of vaccines technologies and platforms:Legacy and newer vaccine technologies, large molecule purification, fermentation technology, viral production, antigen blending, formulation, and sterile filling technology
  • Experience with EU GMP regulations in a manufacturing environment
  • Registration and validation of new products
  • Running a technical agenda to improve product and/or analytical capability
  • Ability to build collaborative relationships with multiple functional stakeholders
  • Ability to influence, direct and develop people and cross-functional team working
  • Additional relevant experience in any of the following associated disciplines such as Manufacturing, Development, Engineering, Quality Control, Quality Assurance, Advanced Project Management, or Regulatory, is desirable
  • Fluency in written and spoken English, some experience in German, any other language in addition is a plus
The offer:
  • Permanent role with a top employer
  • Very attractive salary
  • International work environment with challenging tasks
  • Engaging and inspiring culture with “Play to Win” mentality
Please use our online-application form only for applying to advertised positions. Please note that we can´t consider applications that we receive by e-mail.
Andreas Dürr, E-Mail: aduerr@antal.com, Tel. 0911/59059644

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