Automation Expert

Automation Expert

 

Job Description

An organisation is seeking an Automation Expert to support operations across multiple projects focused on automation systems, specifically MES and DeltaV. In this role, you will support the implementation of automation solutions, independently execute testing and documentation activities, and ensure compliance with cGMP requirements.

You will work closely with the plant and equipment teams to ensure cGMP-compliant documentation, support effective information exchange and communication within the operations group, and implement system changes in line with GMP-compliant change management processes using the available systems.

 

Essential Requirements

· Strong IT skills

· Experience or knowledge of DeltaV and MES systems (advantageous)

· Solid cGMP knowledge

· Knowledge of biopharmaceutical production environments (advantageous)

· Strong ability to collaborate with internal interfaces and team members

· Strong organisational skills

· High level of flexibility in working hours and tasks

· Strong team orientation and high level of commitment

· Fluent German

· Basic knowledge of English

Preferred Requirements

· Experience in automation projects within regulated (cGMP) environments

· Prior exposure to biopharmaceutical production settings

· Experience working with change management processes in GMP environments

 

Practicalities

Start Date: ASAP

Location: Visp, Switzerland

Department: SPM Microbial (MCRB)

 

Interested? Send your CV to Miguel Gomes at m.gomes@panda-int.com or call +31 (0)20 2044 502 / +41 (0)44 5514 407 to discuss the opportunity.

Automation Expert

 

Job Description

An organisation is seeking an Automation Expert to support operations across multiple projects focused on automation systems, specifically MES and DeltaV. In this role, you will support the implementation of automation solutions, independently execute testing and documentation activities, and ensure compliance with cGMP requirements.

You will work closely with the plant and equipment teams to ensure cGMP-compliant documentation, support effective information exchange and communication within the operations group, and implement system changes in line with GMP-compliant change management processes using the available systems.

 

Essential Requirements

· Strong IT skills

· Experience or knowledge of DeltaV and MES systems (advantageous)

· Solid cGMP knowledge

· Knowledge of biopharmaceutical production environments (advantageous)

· Strong ability to collaborate with internal interfaces and team members

· Strong organisational skills

· High level of flexibility in working hours and tasks

· Strong team orientation and high level of commitment

· Fluent German

· Basic knowledge of English

Preferred Requirements

· Experience in automation projects within regulated (cGMP) environments

· Prior exposure to biopharmaceutical production settings

· Experience working with change management processes in GMP environments

 

Practicalities

Start Date: ASAP

Location: Visp, Switzerland

Department: SPM Microbial (MCRB)

 

Interested? Send your CV to Miguel Gomes at m.gomes@panda-int.com or call +31 (0)20 2044 502 / +41 (0)44 5514 407 to discuss the opportunity.