Technical Steward (m/w/d)

Novartis

Schaftenau, Austria
Base: € 65,605.54 / year (minimum collective agree...
On-site
Technology transfer projects
Process validation and improvement
Cgmp and regulatory requirements
Novartis is seeking a Technical Steward for its Schaftenau, Austria location, responsible for technology transfers, process validations, and continuous improvement of pharmaceutical manufacturing processes. The ideal candidate will have a relevant degree and several years of experience in pharmaceutical production, with strong knowledge in cGMP and validation processes

Job Summary

  • Lead and coordinate technology transfer projects (Inbound, Outbound, Scale-up) at the site.
  • Ensure a robust, validated, and continuously improved production process throughout the product lifecycle.
  • Provide technical support as a Subject Matter Expert (SME) for specific pharmaceutical processes or technologies.

Matching Summary

Match Score: 85

Novartis is seeking a Technical Steward for its Schaftenau, Austria location, responsible for technology transfers, process validations, and continuous improvement of pharmaceutical manufacturing processes. The ideal candidate will have a relevant degree and several years of experience in pharmaceutical production, with strong knowledge in cGMP and validation processes.

Salary

Base: € 65,605.54 / year (minimum collective agreement); Bonus/Equity: Attractive bonus/incentive program; Benefits: Modern company pension, childcare facilities, training and development programs, worldwide career opportunities

Skills & Requirements

Must-have

  • Technology transfer projects
  • Process validation and improvement
  • cGMP and regulatory requirements
  • Data analysis for process optimization
  • Subject Matter Expert (SME) support
  • Scientific experiment design and interpretation

Nice-to-have

  • Cross-functional collaboration
  • Knowledge transfer between sites
  • Audit and inspection support

Key Requirements

  • Bachelor's or Master's degree in pharmacy, chemistry, biotechnology, or related field
  • Several years of experience in pharmaceutical production, technology transfer, or MS&T
  • Sound knowledge of cGMP, validation, and regulatory requirements
  • Analytical thinking and experience in statistical process control
  • Strong communication and project management skills
  • Very good German and English skills

Work Rights

Not specified

Tailored Resume

Cover Letter