MSAT Upstream Process Development Expert

Skills Alliance; Stuttgart; Vor Ort; EUR 75.000 - 90.000; Vollzeit

Zusammenfassung

A Biologics CDMO is seeking an experienced Upstream Process Development Manager to lead MSAT teams and oversee process development in Stuttgart. The ideal candidate will have over 6 years of experience in biotech or pharma, with proven skills in upstream process characterisation. This role offers a unique opportunity to contribute to innovative biologics manufacturing and provides excellent career progression within a collaborative team.

Qualifikationen

• 6+ years’ experience in CDMO, Biotech or Pharma.
• Proven expertise in upstream process characterisation.
• Track record working in MSAT teams.

Aufgaben

• Lead and mentor MSAT technical teams.
• Oversee upstream process development and optimisation.
• Collaborate with QA, QC, Regulatory, and Manufacturing teams.

Kenntnisse

Leadership

Process Development

Continuous Improvement

Cross-functional Collaboration

Jobbeschreibung

Overview

We are currently partnered with an established and rapidly growing Biologics CDMO seeking an Upstream Process Development Manager to strengthen its MSAT team based in Germany. This person will have a hands-on role in leading the process development activities supporting innovative biologics manufacturing.

The Role

• Lead and mentor MSAT technical teams, driving innovation and operational excellence
• Oversee upstream process development, optimisation, and scale-up for biologics
• Deliver robust cell culture process characterisation and ensure smooth tech transfer into GMP manufacturing
• Troubleshoot and manage lifecycle activities, embedding a culture of continuous improvement
• Collaborate with QA, QC, Regulatory, and Manufacturing teams to support compliance and regulatory submissions

Your Background

• 6+ years’ experience in CDMO, Biotech or Pharma
• Proven expertise in upstream process characterisation, including scale-up and tech transfer
• Track record working in MSAT teams, supporting GMP commercial manufacturing
• Strong cross-functional collaboration skills with QA, QC, and Regulatory interfaces
• Leadership experience with the ability to mentor and develop scientists / engineers

Why Join

This is a unique opportunity to take on a high-impact leadership role within a fast-growing CDMO, contributing directly to the advancement of cutting-edge biologics. You’ll join a collaborative, innovative team with excellent long-term career progression.

Please apply to this job posting and if there could be a fit, I\'ll look forward to discussing!