MSAT Engineer: Pharma Process Optimization & Transfers

Ophtapharm, a Sentiss Company; Winterthur; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Benefits dieser Stelle

Pension scheme

Free parking

Public transport access

Zusammenfassung

Ophtapharm AG in Switzerland is seeking a skilled MSAT specialist to join its expanding CMO-focused team. You will drive manufacturing process support, optimization, and transfers across the product lifecycle, collaborating with cross-functional groups to ensure robust and compliant operations.

Ideal candidates hold a life sciences related degree and have several years’ GMP pharma experience, with hands-on expertise in process validation or improvement.

Qualifikationen

• Degree in Life Sciences, Pharmacy, Process Engineering, or related field.
• Several years of GMP-regulated pharma experience.
• Hands-on experience in manufacturing support, process validation, or process improvement.
• Sterile manufacturing experience is a plus.
• Fluent in English and German.

Aufgaben

• Drive manufacturing process support, implementation activities, and process changes across the product lifecycle.
• Analyze process performance data and turn insights into tangible improvements.
• Support process validation and continued process verification activities.
• Identify and implement process optimization initiatives together with cross-functional teams.
• Provide technical leadership for product transfers and manufacturing improvement projects.

Kenntnisse

GMP experience

Manufacturing support

Process validation

Process improvement

Sterile manufacturing

English

German

Ausbildung

Degree in Life Sciences/Pharmacy/Process Engineering

Jobbeschreibung

Ophtapharm AG in Switzerland is seeking a skilled MSAT specialist to join its expanding CMO-focused team. You will drive manufacturing process support, optimization, and transfers across the product lifecycle, collaborating with cross-functional groups to ensure robust and compliant operations.

Ideal candidates hold a life sciences related degree and have several years’ GMP pharma experience, with hands-on expertise in process validation or improvement.