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Quality Assurance Engineer in Sunnyvale, California at Cepheid

Date Posted: 4/16/2019

Job Snapshot

Job Description

Job ID: CEP002458

About Us

At Cepheid, we are passionate about improving healthcare through faster, more accurate diagnostic tests. With our GeneXpert® System, we’ve taken the most sophisticated molecular technology and packaged it into an automated, easy-to-use format that has quickly become the platform of choice worldwide. From the largest laboratories to small physician offices, our game-changing solution delivers critical answers when clinicians and patients need them most. Through strong molecular biology capabilities and ongoing product innovation, we are focused on developing tests for healthcare-associated infections, sexual health, critical infectious disease, virology, and oncology applications. Come join our vision for a better way and help make life better for us all! For more details, visit us at www.cepheid.com or follow us on Twitter (@CepheidNews).


Description

Basic Function and Scope of the Position:


Quality Engineer provides support to Cepheid’s manufacturing operations and

contract manufacturers, change controls, process validations, complaint

handling, failure investigations, assigned projects and quality programs, to

ensure that all diagnostic and RUO products are built in accordance with

customer, corporate and regulatory requirements.


Tasks and Responsibilities:


Support manufacturing, contract manufacturing, and complaint handling/field

sustaining leading to improved compliance with corporate policies,

21CFR820, ISO 13485, the Medical Device Directive, and other applicable

regulatory agencies, while striving for continuous improvement.

NPI and Change Control Activities:

Ensure that DMRs are complete and accurate as part of

NPI/design transfer to manufacturing.

Review ECOs and deviations according to change order

guidelines, ensuring impact for “Major” change(s) is outlined

and evidence of required activities, and reason for change is

clear and accurate.

Ensure maintenance of validated state, and consideration for

re-validation during various design and process changes.

Ensure maintenance of product ID and traceability, including

that of safety critical parts.

Review and approve the criteria for WIP reworks and reinspections.

Drive improvements in process capability and quality of

products.

Regularly monitor, investigate and review nonconformance

activities and generate CAPAs/SCARs based on trends/issues

identified from operations, MRB and drive them to closure.

Investigate failures for field/customer, in-coming and inprocess

problems and execute corrective actions.

Process Validation and Manufacturing Process Support

Provide support to process validation and other processes on

the manufacturing floor, warehouse and facilities as required.


Quality System Support:


Support global initiatives/QSIPs and ensure that required
activities are carried out, including pertinent personnel
planning, training and resourcing.
All listed tasks and responsibilities are deemed as essential functions to this
position; however, business conditions may require reasonable
accommodations for additional task and responsibilities.

Job Requirements



Qualifications

Minimum Education Required:


Bachelor degree in a technical field desired, preferably

Mechanical Engineering


Minimum Experience Required:


5-7 years experience in quality assurance field in a medical

device manufacturing environment

In-depth knowledge of SPC, and process capability studies.

Working knowledge of the FDA medical device Quality

Systems Regulations and ISO 13485.

Experience with failure investigations, risk management and

failure report writing,

Excellent written and oral communication skills

Ability to create concise, accurate report

Ability to read technical reports and specifications

Proficiency in the use of personal computers and computer

database software, including Microsoft Office applications

(Access, Excel, Word and PowerPoint).

Must have capability to review, analyze, summarize and

interpret quality systems data, draw conclusions,

interpret quality systems data, draw conclusions, make

appropriate decisions and recommendations, write reports

and give oral presentations.

Must show self-initiative but be comfortable in the role of a

team player. Must be able to manage multiple projects and

report progress against goals in an objective manner

Project management experience

Excellent written, verbal and organizational skills required

Must be detail oriented and able to work independently

Minimum travel is required.

Preferred Requirements:

ASQ certification

Visio and Project knowledge desirable.



Danaher Corporation Overview

Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries, including life sciences, medical diagnostics, dental, environmental and applied solutions. Our globally diverse team of 71,000 associates is united by a common culture and operating system, the Danaher Business System, which serves as our competitive advantage. We generated $19.9B in revenue last year. We are ranked #162 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 5,200% over 25 years.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team.
Danaher is committed to competitive compensation that typically has key components including base salary, variable annual incentive compensation based on personal and company performance, and long-term incentive.