Job Details

ID #51761090
Estado California
Ciudad Santarosa
Full-time
Salario USD TBD TBD
Fuente J&J Family of Companies
Showed 2024-05-23
Fecha 2024-05-23
Fecha tope 2024-07-22
Categoría Etcétera
Crear un currículum vítae
Aplica ya

QA Technician III

California, Santarosa, 95401 Santarosa USA
Aplica ya

QA Technician III - 2406189340WDescriptionAuris Health a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Technician III located in Santa Rosa, CA.At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/ .The Quality Technician is responsible for assuring that company products have been manufactured, inspected, and tested using company approved procedures. Work with manufacturing and QA to implement solutions to quality related problems.Description of WorkPerform a wide variety of audits, inspections, checks, tests, and sampling procedures to ensure quality of manufactured goods and adherence to quality procedures. Maintain “qualified” status on all quality audits, inspections, testing, and equipment procedures. Coordinate training/cross-training of new and/or existing employees. With direction from supervisor, coordinate quality activities (i.e., inspections, testing, audits) based on manufacturing and/or Research & Development activities. Alert supervisor and/or department engineer of any situation that prevents the Quality Technicians from achieving optimum efficiency. Work with department engineers on development/modification of test methods for new and/or existing products. Write and update inspection procedures and checklists as required. Propose document changes, as necessary, to supervisor or engineers to ensure GMP compliance. Check lot history records for completeness, accuracy, and conformance to SOP. Monitor calibration and maintenance of all test equipment and fixtures and operation of equipment. In partnership with manufacturing, implement visual standards and limit samples related to WIP and final inspection of product. Maintain thorough knowledge of all testing related to set-up, in-process, final inspection, and lot release testing. Support implementation of corrective actions related to internal/external audits.QualificationsRequired Skills & Experience

High school diploma

5 years relevant experience in medical devices

Problem-solving skills

Clear communication, both written and verbal

Work well with others

Flexible and adaptable – comfortable working in a dynamic environment

Preferred Skills & Experience

Ability to adapt quickly and deal calmly within an environment in which changes can occur frequently.

Ability to be self-motivated and self-directed while maintaining good communication with the rest of the team.

Travel Expectations§ Travel not anticipated.About LaminarLaminar is a clinical stage medical device company advancing transseptal left atrial appendage (LAA) closure. The LAA is a small pouch in the left atrium of the heart that is a major contributor to thromboembolic stroke in patients with atrial fibrillation. It has developmental, ultra-structural, and physiological characteristics distinct from the left atrium proper. Growing incidence of atrial fibrillation and medical device developments have rapidly expanded the market.Schedule: M-F 8am-5pmAdditional Information:

The anticipated base pay range for this position is $48,000 to $86,000

This position is overtime eligible

This position is eligible for a shift differential.

Employees are eligible for the following time off benefits:

Vacation – up to 120 hours per calendar year

Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year

Holiday pay, including Floating Holidays – up to 13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefitsThis job posting is anticipated to close on May 29, 2024. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com .Primary Location NA-US-California-Santa RosaOrganization Biosense Webster Inc. (6010)Job Function Quality ControlReq ID: 2406189340W

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