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Quality Control Technician 2

  • Flanders (Suffolk County)
  • IT development

Job description

Locations:Flanders, New Jersey
Job Family:Research & Development

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English (US)

Job Description

Division: Siemens Healthineers
Business Unit: Laboratory Diagnostics
Requisition Number: 233648
Primary Location: United States-New Jersey-Flanders
Assignment Category: Full-time regular
Experience Level: Mid level
Education Required Level: Associate's Degree / College Diploma
Travel Required: 10%

Division Description:

At Siemens Healthineers, we are passionate about enabling healthcare professionals to deliver high quality patient care, and to do so affordably. A leading global healthcare company, Siemens Healthineers continues to strengthen our portfolio of medical imaging and laboratory diagnostics, while adding new offerings such as managed services, consulting, and healthcare IT services – as well as further technologies in the growing market for therapeutic and molecular diagnostics.

Siemens Healthineers develops innovations that support better patient outcomes with greater efficiencies, giving providers the confidence they need to meet the clinical, operational and financial challenges of a changing healthcare landscape.

Job Description:

The Product Final Release Technician will support the release of finished product. The position interacts with all levels of employees and management. The nature of these interactions includes answering release criteria questions, problem solving and quality and compliance issues. This position requires independent thinking, interpersonal and communication skills. The problems are usually technical, quality or compliance related in nature.

ESSENTIAL JOB FUNCTIONS:

1. Manages and maintains quality documents related to the final release of instruments.
2. Reviews all medical device test data and Device History Records to ensure all required specifications are met prior to product release.
3. Acts as a liaison between Production and Engineering in the resolution of release criteria.
4. Ensures documentation requirements are met according to Operating Procedures, QSR and ISO standards.
5. Ensures failure analysis, re-test and corrective actions are documented.
6. From time to time, the incumbent's supervisor/manager may assign additional unlisted duties/responsibilities on a temporary or regular basis depending on business needs.
7. Incumbent is responsible for understanding the Quality Management System.

Associate's Degree in technology or equivalent program, or completion of a Technical School with at lease two to five years of relevant experience or the equivalent in related work experience.

Experience on Final Inspection related activities in a medical device manufacturing environment preferred.

Must be able to effectively communicate with Engineering, Production personnel, Supplier Operations and Materials in order to communicate and resolve final inspection issues.

Equal Employment Opportunity Statement
Siemens is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, protected veteran or military status, and other categories protected by federal, state or local law.

EEO is the Law
Applicants and employees are protected under Federal law from discrimination. To learn more,Click here .

Pay Transparency Non-Discrimination Provision
Siemens follows Executive Order 11246, including the Pay Transparency Nondiscrimination Provision. To learn more,Click here .

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