Manufacturing Science & Technology Expert (MSAT)

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

At Ophtapharm AG, we develop and manufacture high-quality ophthalmic medicines for patients around the world. As an FDA and EU-GMP certified pharmaceutical manufacturer, we are entering an exciting new phase of growth as we expand our Contract Manufacturing Organization (CMO) business.

As part of our MSAT Team, you will play a key role in ensuring robust, efficient, and compliant manufacturing processes across the product lifecycle. From process optimization to product transfers, your expertise will help bring new products into commercial production and support Ophtapharm's growth journey.

Your Role

• 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.

Your Profile

• Degree in Life Sciences, Pharmacy, Process Engineering, or a related field.
• Several years of experience within a GMP-regulated pharmaceutical environment.
• Hands-on experience in manufacturing support, process validation, or process improvement.
• Strong understanding of pharmaceutical manufacturing processes; sterile manufacturing experience is a plus.
• Fluent in English and German.

What you can expect

• A unique opportunity to shape the future of Ophtapharm as it expands its Contract Manufacturing Organization (CMO) business.
• A broad and visible role with exposure across products, processes, and departments.
• Short decision-making paths and direct collaboration with key stakeholders.
• The freedom to influence processes, improvements, and ways of working.
• Attractive pension scheme, free parking, and convenient public transport access.