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Senior Bioprocess Engineer, Downstream Processing (DSP)

lonza · Visp

Nouveau
Onsite Senior 🇬🇧 English
chromatography resin management column packing tangential flow filtration GMP documentation root cause analysis CAPA management change control

Description du poste

About the role

Join Lonza's world‑class biomanufacturing site in Visp and lead downstream processing campaigns in a GMP environment. You will combine hands‑on manufacturing support with engineering expertise to ensure safe, compliant and reliable production of life‑changing therapies.

Key responsibilities

  • Serve as senior technical expert for downstream processing manufacturing campaigns, providing shop‑floor support from preparation through close‑out.
  • Lead investigations, root‑cause analyses, CAPAs, change controls and risk assessments to resolve deviations and improve process robustness.
  • Analyze performance data to increase plant throughput, yields, equipment reliability and cycle times.
  • Partner with Manufacturing, MSAT, QA, QC, Validation, Engineering and Supply Chain on technology transfers and process validation.
  • Drive continuous‑improvement initiatives and mentor junior engineers and manufacturing staff.

Required profile

  • 10+ years of GMP downstream processing experience in commercial or late‑stage biopharma manufacturing.
  • Proven expertise in chromatography, purification, TFF/UF‑DF operations and DSP optimization.
  • Strong track record troubleshooting complex process and equipment issues in a regulated environment.
  • Degree in Biotechnology, Chemical Engineering, Bioprocess Engineering or related field, or equivalent experience.
  • Excellent communication, collaboration and stakeholder‑management skills.

Required skills

  • Chromatography systems and resin management
  • Column packing techniques
  • Tangential flow filtration (TFF) and ultrafiltration/diafiltration (UF/DF)
  • GMP documentation, deviation investigation and CAPA management
  • Process data analysis for decision‑making

What we offer

  • Agile career and dynamic working culture within a global life‑sciences leader
  • Opportunities to work on commercial and late‑stage biopharmaceutical processes impacting patients worldwide
  • Inclusive, ethical workplace built on collaboration, accountability and continuous improvement
  • Compensation programs recognizing high performance and technical expertise
  • Benefits dependent on role and location, with relocation assistance available for eligible candidates

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