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GMD Specialist - QA (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
REFERENZNUMMER:
317940/11
IHRE AUFGABEN:
-Order test equipment and GMD from approved suppliers
-Administering test equipment and GMD physically and electronically within local GMD Management System
-Conduct scheduled calibration and maintenance on test equipment and GMD
-Establish maintenance and calibration schedule for test equipment (including 3 D CMM) and GMD based on manufacturers recommendations and maintains equipment records
-Act as the SME for Gage R+R
-Apply principles of Good Documentation Practices
-Provide training on test equipment and (special) GMD
-Provide assistance for the performance of validation activities including application of statistical software
-Implement revisions, corrections and changes to test equipment, procedures and methods
-Issue and execute NCR within the software application
-Act as owner of actions assigned from Quality Systems (NCR, CAPA, Audit Observations)
IHRE QUALIFIKATIONEN:
-Solid working experience within the areas mentioned above
-Practical experience in a regulated industry, preferably in a medical device environment
-Good knowledge of GMD, 3 D CMM, NCR, CAPA and Audit Observations
-Ability to work on multiple tasks simultaneously under limited supervision
-Ability to follow change management for internal guidelines
-Knowhow of quality assurance principles
-English and German spoken and written
WEITERE QUALIFIKATIONEN:
Quality manager
317940/11
IHRE AUFGABEN:
-Order test equipment and GMD from approved suppliers
-Administering test equipment and GMD physically and electronically within local GMD Management System
-Conduct scheduled calibration and maintenance on test equipment and GMD
-Establish maintenance and calibration schedule for test equipment (including 3 D CMM) and GMD based on manufacturers recommendations and maintains equipment records
-Act as the SME for Gage R+R
-Apply principles of Good Documentation Practices
-Provide training on test equipment and (special) GMD
-Provide assistance for the performance of validation activities including application of statistical software
-Implement revisions, corrections and changes to test equipment, procedures and methods
-Issue and execute NCR within the software application
-Act as owner of actions assigned from Quality Systems (NCR, CAPA, Audit Observations)
IHRE QUALIFIKATIONEN:
-Solid working experience within the areas mentioned above
-Practical experience in a regulated industry, preferably in a medical device environment
-Good knowledge of GMD, 3 D CMM, NCR, CAPA and Audit Observations
-Ability to work on multiple tasks simultaneously under limited supervision
-Ability to follow change management for internal guidelines
-Knowhow of quality assurance principles
-English and German spoken and written
WEITERE QUALIFIKATIONEN:
Quality manager
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges