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Senior Qualifying Specialist

m/w/d, Wallis

Are you experienced in validation of equipment and facilities within pharmaceutical environment?

Here is a great opportunity to apply your knowledge and support global projects.

Duration: 31.12.2024 (extension most likely)

Your tasks:

Prepare validation documents. Execution of IQ/OQ and PQ for equipment, systems and utilities.
Write reports of completed validation activities.
Work to identify efficiencies in the validation program approach.
Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s.
Writing and/or revising procedures applicable to the Engineering activities.
Support the Engineering group to prepare the validation, requalification, and maintenance program.

Your background:

Advanced Level Pharma Industry minimum 5 years experience.
Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner.
Excellent German - written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties.