Process Expert – MSAT / Manufacturing Science & Technology

Adryan; Basel; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Adryan is seeking an experienced Process Expert – MSAT to support a client in Basel, Switzerland. The role focuses on the implementation, optimization and continuous improvement of sterile manufacturing processes in a GMP environment.

You will work closely with Manufacturing, Engineering and Quality to ensure processes and equipment are effectively implemented, documented and maintained in a GMP-regulated setting. This is a hands-on process role requiring practical, quality-focused work.

Qualifikationen

• University/technical degree in a relevant technical field.
• GMP-regulated pharmaceutical or life sciences experience.
• Experience with MSAT, process engineering or manufacturing.
• Sterile/aseptic manufacturing experience is desirable.
• Hands-on implementation or improvement of manufacturing processes/equipment.
• GMP documentation and deviations/change controls experience.
• MES and SAP familiarity.

Aufgaben

• Develop, implement and improve manufacturing processes in sterile production.
• Support new processes, equipment and manufacturing technologies.
• Provide technical support for manufacturing activities including filling and in-process controls.
• Create and maintain SOPs, batch records and MES documentation.
• Ensure GMP compliance and validated process parameters.
• Identify opportunities for process optimization and continuous improvement.
• Assist with deviations, investigations and change controls.
• Collaborate with Manufacturing, Engineering and Quality to resolve issues.
• Support internal and customer audits and regulatory inspections.

Kenntnisse

MSAT

GMP knowledge

Sterile manufacturing

Process engineering

Documentation

SAP

MES

MS Office

Cross-functional teamwork

Analytical thinking

Ausbildung

University or technical college degree in Pharmaceutical Technology, Chemistry, Biology, Biotechnology, Engineering or related technical discipline

Tools

MES

SAP

Jobbeschreibung

Industry: Pharmaceutical / Life Sciences

Duration: 4 months with possibility of extension

Process Expert – MSAT / Manufacturing Science & Technology

About us

Adryan is an internationally operating services group with offices in The Netherlands and Switzerland. We specialize in providing a full range of services for the life sciences industry, focusing on Project Management, Technical Operations, CQV, and Compliance. Our teams work with top clients in the life sciences sector, ensuring the highest quality and commitment.

About the Role

Adryan is looking for an experienced Process Expert – MSAT (Manufacturing Science & Technology) to support our client in Basel Switzerland.

The role focuses on the implementation, optimization and continuous improvement of manufacturing processes, with a particular focus on sterile production.

You will work closely with Manufacturing, Engineering, Quality and other technical functions to ensure that processes and equipment are effectively implemented, documented and maintained in a GMP-regulated environment.

This is a hands-on process and manufacturing role.

Key Responsibilities

• Develop, implement and improve manufacturing processes and procedures within a sterile production environment.
• Support the implementation of new processes, equipment and manufacturing technologies.
• Provide technical support for manufacturing activities including preparation, filling, in-process controls and batch documentation.
• Create and maintain SOPs, process documentation and electronic batch records (MES).
• Ensure manufacturing processes are operated in accordance with GMP requirements and validated process parameters.
• Identify opportunities for process optimization and continuous improvement.
• Support investigations of deviations, process issues and change controls.
• Work closely with Manufacturing, Engineering and Quality to resolve technical and process-related issues.
• Support internal and customer audits from a process and technical perspective.
• Provide technical support during customer visits and regulatory inspections when required.
• Support projects involving the implementation of new equipment, processes and manufacturing procedures.
• Contribute to maintaining the validated state and robustness of manufacturing processes.

Your Profile

• University or technical college degree in Pharmaceutical Technology, Chemistry, Biology, Biotechnology, Engineering or a related technical discipline.
• Professional experience in a GMP-regulated pharmaceutical or life sciences environment.
• Experience in MSAT, process engineering, manufacturing science, process technology or pharmaceutical manufacturing.
• Experience in sterile or aseptic manufacturing is highly desirable.
• Practical experience with the implementation or improvement of manufacturing processes and/or equipment.
• Good understanding of GMP and validated manufacturing processes.
• Experience with deviations, change controls and GMP documentation.
• Familiarity with MES and SAP.
• Good knowledge of MS Office.
• Experience working in cross-functional project teams.
• Fluent English is required.
• German is an advantage but not essential.

Personal Attributes

• Strong problem-solving and solution-oriented mindset.
• Practical and hands-on approach.
• High level of attention to quality, compliance and detail.
• Structured and reliable way of working.
• Strong communication and stakeholder management skills.
• Comfortable working independently and taking ownership.
• Professional interaction with colleagues, customers and external stakeholders.