DSP MSAT Process Expert

DSP MSAT Process Expert

Visp, Switzerland – Full-time

Company Description

This global biopharmaceutical leader, based in Visp, Switzerland, specializes in cutting-edge development and large-scale manufacturing of biologics. The site is recognized for its innovation, GMP excellence, and ability to deliver advanced therapies to patients worldwide. The MSAT (Manufacturing Science and Technology) team plays a central role in technology transfer, process optimization, and ensuring seamless integration of novel processes into commercial manufacturing.

Job Description

As a
DSP MSAT Process Expert
, you will be a driving force in ensuring robust and compliant downstream processes through technology transfer and process excellence initiatives. Acting as a bridge between customers, development teams, and operations, you will support projects from design through full-scale manufacturing, resolve process challenges, and ensure smooth execution of campaigns. Your role will be pivotal in implementing innovative solutions, optimizing existing processes, and maintaining the highest standards of GMP compliance.

Key Responsibilities:

• Support end-to-end
  technology transfers
  , from process design to scale-up and manufacturing implementation.
• Act as the
  key interface
  between customers, process donors, and internal operations teams to ensure scalability and manufacturability.
• Oversee
  campaign execution
  , including direct customer communication, reporting of batch performance, and ensuring smooth campaign closure.
• Investigate and resolve process-related issues
  , maintaining compliance with GMP and regulatory expectations.
• Manage
  process documentation
  , including campaign reports, material change requests, and deviation handling.
• Drive
  innovation and optimization
  by facilitating the implementation of new materials and enhancing existing processes.

Essential Requirements:

• Bachelor\’s or Master\’s degree in Biotechnology, Chemical Engineering, or related fields (PhD preferred).
• Minimum 5 years\‘ experience in biopharma manufacturing or process development, ideally within
  Mammalian Manufacturing and MSAT
  .
• Solid expertise in process validation, cleaning validation, material management, and deviation handling.
• Strong knowledge of GMP and bioprocess technologies.
• Fluent English; German language skills are a strong advantage.
• Proven leadership, communication, and organizational skills with a collaborative, solution-driven mindset.
• Agile, motivated, and capable of working independently while fostering teamwork.

Additional Insights:

• Location: Visp, Switzerland (on-site role with up to 2 days/week home office possible)
• Contract Type: 6 months with the possibility of extension
• Start Date: ASAP

Interested?

Send your CV to
Khanyi Mabena
at
k.-
or reach out directly at
to learn more.