Description
* Neuenburg, Neuchâtel
* Temporär
Job Details
For our client, an international company based in Zürich, we are looking for a Process Packaging Engineer.
General Information:
* Start date: ASAP
* End date: 21/01/2025
* Workplace: Zürich (hybrid role)
* Workload: 100%
Tasks and responsibilities:
Scope of work includes all commercial products in the Oncology, Small Molecule portfolio, packaged within the internal Packaging Network and approved contract manufacturing organizations (CMO-s) throughout the company global footprint.
The person will manage CMO activities including all the documentation requirements of Packaging operations.
Your profile:
* Knowledge of cGMP documentation requirements
* At least a Bachelor-s Degree in an engineering related field
* Minimum 5 years of pharmaceutical experience (or equivalent)
* Knowledge and experienced use of Trackwise
* Knowledge of developing and experience in qualifying packaging components on packaging equipment
* Experience in management (development, review and approval of) new and modifications to technical profile drawings and purchasing/release specifications
* Ability to multi task and achieve tactical deliverables with little to no supervision, while understanding strategic impact training
* Strong technical, interpersonal, communication and leadership skills
* Lead or own change control, non-conformances and CAPA activities working with Quality and Global Labeling Operations.
Requirements:
* Pharmaceutical Packaging:
* Oral Solid Dose
* Vials Blisters and Bottles
* Serialization
* Liquid and Powder fill/finish
* Quality Management Documentation Systems: Trackwise (version 10)
* Artwork management systems (BLUE) or other automated systems
For our client, an international company based in Zürich, we are looking for a Process Packaging Engineer.
General Information:
* Start date: ASAP
* End date: 21/01/2025
* Workplace: Zürich (hybrid role)
* Workload: 100%
Tasks and responsibilities:
Scope of work includes all commercial products in the Oncology, Small Molecule portfolio, packaged within the internal Packaging Network and approved contract manufacturing organizations (CMO-s) throughout the company global footprint.
The person will manage CMO activities including all the documentation requirements of Packaging operations.
Your profile:
* Knowledge of cGMP documentation requirements
* At least a Bachelor-s Degree in an engineering related field
* Minimum 5 years of pharmaceutical experience (or equivalent)
* Knowledge and experienced use of Trackwise
* Knowledge of developing and experience in qualifying packaging components on packaging equipment
* Experience in management (development, review and approval of) new and modifications to technical profile drawings and purchasing/release specifications
* Ability to multi task and achieve tactical deliverables with little to no supervision, while understanding strategic impact training
* Strong technical, interpersonal, communication and leadership skills
* Lead or own change control, non-conformances and CAPA activities working with Quality and Global Labeling Operations.
Requirements:
* Pharmaceutical Packaging:
* Oral Solid Dose
* Vials Blisters and Bottles
* Serialization
* Liquid and Powder fill/finish
* Quality Management Documentation Systems: Trackwise (version 10)
* Artwork management systems (BLUE) or other automated systems