Jobdetails

For one of our clients, a leading global pharmaceutical company in Kaiseraugst, we are currently looking for an Asset Excellence Manager (Process Manager).

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General Information:

Start date: ASAP

Latest possible start date: in 3 months

Duration: 12 months with the possibility of extension

Workplace: Kaiseraugst

Workload: 100%

Remote/Home Office: Yes, maximum 1 day per week

Working hours: Standard, on-call duty possible

Department: Sterile Filling, Asset Prefilled Syringes

About the job:

The Asset Pre-Filled Syringes department is part of sterile production at the Kaiseraugst production center. Protein solutions for various commercial products are filled into glass syringes using sterile filtration. The production area operates in 5 shifts. The production team consists of approximately 60 employees. As Asset Excellence Manager, you will oversee the production area and be involved in the release process for the manufactured batches.

Your Profile:

Completed training in the food or pharmaceutical sector or a university degree in a natural sciences (e.g., pharmacy or chemistry).

Several years of experience in production – ideally in the manufacture of sterile dosage forms.

Well versed in GMP regulations, proficient in batch record review as well as deviation, change, and CAPA management, and have in-depth IT knowledge, particularly in the use of MES systems such as PMX or PharmaSuite.

Fluent German and English skills

Tasks & responsibilities:

Responsible for processing deviations and complaints as deviation owner

Supporting the lines with compliance issues

Creating and maintaining GMP documents in compliance with the applicable regulations

Responsible for processing changes as change owner

Responsible for processing deviations and complaints

Responsible for processing CAPA

Collaboration on projects

Carrying out or supporting tests/validation of systems

Planning and carrying out APS (Aseptic Process Simulation) and service life validations

Collaboration in the creation and testing of recipes and manufacturing instructions

Representing the department as an SME during inspections and audits

Optimizing operational processes to increase capacity through the use of LPS tools

Must haves:

Completed vocational training, preferably in the food or pharmaceutical sector; Bachelor's or Master's degree in the natural sciences (e.g. pharmacist or chemistry)

Several years of experience in production (preferably manufacturing sterile dosage forms); also possible as an entry-level position

Experience in batch record review

Experience in a regulated GMP environment

Experience in deviation management, change control, complaint management; CAPA Management

IT knowledge (especially MES (PMX. PharmaSuite)

German language skills (absolute must have), fluent in English

Sounds interesting? Apply now – we’re looking forward to receiving your applications!

Application Submission Deadline: 12.09.2025

mehr anzeigen

For one of our clients, a leading global pharmaceutical company in Kaiseraugst, we are currently looking for an Asset Excellence Manager (Process Manager).

General Information:

Start date: ASAP

Latest possible start date: in 3 months

Duration: 12 months with the possibility of extension

Workplace: Kaiseraugst

Workload: 100%

Remote/Home Office: Yes, maximum 1 day per week

Working hours: Standard, on-call duty possible

Department: Sterile Filling, Asset Prefilled Syringes

About the job:

The Asset Pre-Filled Syringes department is part of sterile production at the Kaiseraugst production center. Protein solutions for various commercial products are filled into glass syringes using sterile filtration. The production area operates in 5 shifts. The production team consists of approximately 60 employees. As Asset Excellence Manager, you will oversee the production area and be involved in the release process for the manufactured batches.

...

Your Profile:

Completed training in the food or pharmaceutical sector or a university degree in a natural sciences (e.g., pharmacy or chemistry).

Several years of experience in production – ideally in the manufacture of sterile dosage forms.

Well versed in GMP regulations, proficient in batch record review as well as deviation, change, and CAPA management, and have in-depth IT knowledge, particularly in the use of MES systems such as PMX or PharmaSuite.

Fluent German and English skills

Tasks & responsibilities:

Responsible for processing deviations and complaints as deviation owner

Supporting the lines with compliance issues

Creating and maintaining GMP documents in compliance with the applicable regulations

Responsible for processing changes as change owner

Responsible for processing deviations and complaints

Responsible for processing CAPA

Collaboration on projects

Carrying out or supporting tests/validation of systems

Planning and carrying out APS (Aseptic Process Simulation) and service life validations

Collaboration in the creation and testing of recipes and manufacturing instructions

Representing the department as an SME during inspections and audits

Optimizing operational processes to increase capacity through the use of LPS tools

Must haves:

Completed vocational training, preferably in the food or pharmaceutical sector; Bachelor's or Master's degree in the natural sciences (e.g. pharmacist or chemistry)

Several years of experience in production (preferably manufacturing sterile dosage forms); also possible as an entry-level position

Experience in batch record review

Experience in a regulated GMP environment

Experience in deviation management, change control, complaint management; CAPA Management

IT knowledge (especially MES (PMX. PharmaSuite)

German language skills (absolute must have), fluent in English

Sounds interesting? Apply now – we’re looking forward to receiving your applications!

Application Submission Deadline: 12.09.2025

mehr anzeigen