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About the Role
**Thoratec Switzerland GmbH** , part of **Abbott Laboratories,** is a global leader in life-saving medical technologies. Our innovative systems, developed and manufactured in Zurich, support patients with advanced heart failure. With around 130 colleagues in development, quality, and production, we work together to make a real difference in people’s lives.
**Main Responsibilities:**
**Process Validations and Equipment Qualification:**
+ Collaborate with Manufacturing Engineering to validate processes and qualify equipment.
+ Evaluate, review, and approve validation and qualification plans, reports, and risk files.
**Non-Conforming Material (NCMR) Handling:**
+ Manage the complete handling of non-conforming materials (NCMR).
+ Develop and implement corrective and preventive actions (CAPA) based on NCMR findings.
+ Document, track, and trend NCMRs, ensuring timely and effective corrections.
+ Collaborate with cross-functional tea...
**Main Responsibilities:**
**Process Validations and Equipment Qualification:**
+ Collaborate with Manufacturing Engineering to validate processes and qualify equipment.
+ Evaluate, review, and approve validation and qualification plans, reports, and risk files.
**Non-Conforming Material (NCMR) Handling:**
+ Manage the complete handling of non-conforming materials (NCMR).
+ Develop and implement corrective and preventive actions (CAPA) based on NCMR findings.
+ Document, track, and trend NCMRs, ensuring timely and effective corrections.
+ Collaborate with cross-functional tea...
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