Manufacturing Engineer. in Glattbrugg

We are currently supporting our client, an important company in the life sciences sector, in the search for a Manufacturing Engineer with expertise in MBR (Manufacturing Batch Record) design and validation activities for a project based on PAS-X 3.2.

Temporary Contract managed through Randstad

Contract Duration: 28/07/2025 – 19/12/2025 (with possible extension)

Workload: On-site presence required at least 4 days per week

Languages: Fluent French and English (spoken and written)

Main Responsibilities:

Process SME:

Manage updates and request modifications to MBRs based on evolving manufacturing needs.
Participate in MBR design workshops, providing technical input and ensuring alignment with operational requirements.
Support and execute informal dry runs and formal MBR verification activities.
Execute test orders and review MBRs, delivering feedback to the MBR design team.
Assist in creating and executing MBR verification protocols.
Provide HyperCare support during the MES Go-Live phase.
Contribute to end-user training activities.

Validation Activities:

Support MES validation activities (IQ, OQ, PQ phases), including drafting and executing validation protocols.

MBR Designer:

Ensure that MBRs accurately document the manufacturing process and collect all necessary compliance data.
Create Master Data and manage object status diagrams.
Ensure strict adherence to Global MBR Design Rules.

Profile Requirements:

A minimum of 5 years of experience as an MBR Designer on PAS-X 3.2 projects within life sciences environments.
Excellent communication skills in French and English, both spoken and written.
Availability to work on-site at least 4 days per week.

We are currently supporting our client, an important company in the life sciences sector, in the search for a Manufacturing Engineer with expertise in MBR (Manufacturing Batch Record) design and validation activities for a project based on PAS-X 3.2.

Temporary Contract managed through Randstad

Contract Duration: 28/07/2025 – 19/12/2025 (with possible extension)

Workload: On-site presence required at least 4 days per week

Languages: Fluent French and English (spoken and written)

Main Responsibilities:

Process SME:

Manage updates and request modifications to MBRs based on evolving manufacturing needs.
Participate in MBR design workshops, providing technical input and ensuring alignment with operational requirements.
Support and execute informal dry runs and formal MBR verification activities.
Execute test orders and review MBRs, delivering feedback to the MBR design team.
Assist in creating and executing MBR verification protocols.
Provide HyperCare support during the MES Go-Live phase.
Contribute to end-user training activities.

Validation Activities:

Support MES validation activities (IQ, OQ, PQ phases), including drafting and executing validation protocols.

MBR Designer:

Ensure that MBRs accurately document the manufacturing process and collect all necessary compliance data.
Create Master Data and manage object status diagrams.
Ensure strict adherence to Global MBR Design Rules.

Profile Requirements:

A minimum of 5 years of experience as an MBR Designer on PAS-X 3.2 projects within life sciences environments.
Excellent communication skills in French and English, both spoken and written.
Availability to work on-site at least 4 days per week.

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LS

Luciana Sardo

+41 58 201 55 55
Basel Professionals Life Sciences

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Luciana Sardo

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23453

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Job Details

Firma: Randstad (Schweiz) AG - Randstad Inhouse Services Basel

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