Main Responsibilities:
As a Production Engineer, you will work in a multidisciplinary operational group, mean responsible for the position are:
- Execution of routine validation in the field of microbiology and equipment according to schedule to meet QA standards such as ISO 13485, MDSAP, and FDA requirements.
- Write and rewrite new validation protocols according to need and execute them.
- Install new and existing production equipment in the company production sites across the world, including the purchase of required parts, and work with supp
Requirements: B.Sc. in mechanical engineering, practical engineering in related field or other relevant degree.
- Minimum 2 years of experience as production engineer or related position, in a
medical device company.
- Experience in GMP/GDP working environment.
- The candidate must work well in a team environment across functions and sites.
- Being able to function independently as well as part of a team.
- Communication skills, flexibility, and accuracy
- Strong mechanical aptitude for problem solving and production tool improvement.
-experience in Solidworks and PDM, on complex parts and assemblies
-Knowledge in 3D printing
- hand on attitude
- Experience in Priority.
- Knowledge of MS Office
- Fluent English.
This position is open to all candidates.
