CLS - ARIA DIAGNOSTICS, INC - San Jose, CA

Clinical Laboratory Scientist/Research Associate


RESPONSIBILITIES: The Clinical Laboratory Scientist/RA is responsible for performing high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures and complying with all applicable local, state and federal laboratory 
requirements. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multi-task and be flexible with tasks and schedules and the ability to work independently in a team environment.

Principal responsibilities include:

• Perform laboratory tests, procedures and analyses according to the laboratory's standard operating procedures.
• Perform, review and document laboratory quality control procedures.
• Operate, maintain and troubleshoot laboratory equipment
• Prepare reagents required for laboratory testing.
• Review, interpret and report patient results.
• Independently identify and troubleshoot basic problems that adversely affect test performance.
• Report all concerns of test quality and/or safety to the Supervisor or Safety Officer
• Assist with final development of protocol and processes for a Laboratory Developed Test and perform other duties as assigned.

REQUIREMENTS: We seek an individual with a successful track record who
must be comfortable with a start-up environment.

• Must possess a valid California CLS license, generalist preferred.
• Completion of a CLS training program at an accredited institution or clinical laboratory work experience within the last five years.
• Possess working knowledge of local, state and federal laboratory regulations.
• Computer skills a must, automation skills preferred.
• Ability to analyze and problem solve basic issues that impact test performance.
• Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed.
• Must communicate effectively with coworkers and non-laboratory personnel
• Able to integrate and apply feedback in a professional manner.
• Able to manage daily test processing needs with high emphasis on quality.
• Ability to work as part of a team.
• Ability to perform repetitive tasks.
• High volume laboratory experience preferred.
• Training in molecular biology techniques preferred.

…………………………………………………………..

B. MELISSA KAMITA
Human Resources Manager
ARIA DIAGNOSTICS, INC.
5945 Optical Court
San Jose, CA 95138
mkamita@ariadx.com [1]
DESK: 408-229-7537
FAX: 408-229-7596

Technical Support Specialist --- Cepheid

Job 2795: Technical Support Specialist

As the Technical Support Specialist you will be responsible for providing first line
technical support to Cepheid customers on all Cepheid products and instrument
systems. In addition, you will provide support to field technical support specialists,
field systems engineers, Cepheid commercial professionals, and technical support
professionals located globally in Cepheid offices as well as distributorships. You will
conduct preliminary investigation to resolve issues in a timely manner.

*This is a contract/temporary position.

Responsibilities:

• Provide phone and e-mail technical support for different shifts including weekends and holidays and as schedule demands
• Serve as primary interface with customers contacting Cepheid with technical questions, problems, or complaints.
• Document and update customer reported complains in the CMS related to
• Cepheid systems and products
• Conduct preliminary investigation and data collection for technical problems of diverse scope. Escalate to next level Technical Support Specialist as warranted.
• Follow SOPs to ensure accurate and complete complaint handling and documentation in the Complaint Management System.
• Follow procedures set forth in ISO regulations and QSR for medical device.
• Perform additional tasks as assigned by the Technical Support Manager

Required Knowledge, Skills, and Abilities:

Required Knowledge - Skills:

• BS in Science, Clinical Laboratory Science or relevant certification in clinical laboratory science (i.e. MLT/ MLS).
• 1-2 years of relevant experience in clinical laboratories and/or medical diagnostic industry.
• Knowledge and application of computers, MS Excel, MS Word is a must
• Excellent written/verbal communication and organizational skills.
• Highly organized with attention to details.
• Ability to follow complex procedures and processes
• Highly motivated team player.
• Knowledge of molecular diagnostics is preferred.
• Flexible to work different shifts, weekend and holidays as needed. Primary hours are weekdays: 11:00am – 9:00pm.

The statements in this description represent typical elements, criteria and general
work performed. They are not intended to be an exhaustive list of all
responsibilities, duties, and skills for this job.

Additional Data

Preferred Qualifications:

BS in Science, Clinical Laboratory Science
1-2 years of relevant experience in clinical laboratories and/or medical diagnostic
industry.

Physical Demands:

Flexible to work different shifts, weekend and holidays as needed.
Be able to talk on the phone for up to 6 hours per day.

Senior Technical Support Specialist -- HBDC -- Cephied

As Senior Technical Support, you will be responsible for providing first line technical
support to Cepheid customers on all Cepheid products and instrument systems. In
addition, you will provide support to field technical support specialists, field systems
engineers, Cepheid commercial professionals, and technical support professionals
located globally in Cepheid offices as well as distributorships. You will work closely
with sales and marketing, QA/QC, research and development to address customer
concerns, conduct primary investigations, determine corrective action and customer
follow-up. Your operational responsibility for the Technical Support group will be in
the coordination and support of countries in Cepheid’s HBDC program; primarily in
the Asian and America’s markets.

*This is a contract/temporary position.

Responsibilities:

• Serves as primary customer contact for HBDC clinical laboratories, distributors, Cepheid global business heads, Cepheid marketing HBDC managers and NGO organizations for area of primary responsibility (Asia and the Americas).
• Serve as back up and counterpart to European based HBDC support specialist.
• With HBDC specialist counterpart(s), develop and maintain worldwide accounting of technical support logistics for smooth operations of HBDC business.
• Design and perform technical training for internal and external clients, including specialized training materials and delivery methods for the HBDS market.
• Communicate systems introductions and changes- implement training and support strategies for the technical support group – consistent with plans for assay.
• Prepare technical bulletins or troubleshooting guides for global distribution.
• Manage technical communications with global support teams.
• Support phone and e-mail technical support lines for different shifts, including weekends and holidays as schedule demands.
• Work on technical problems of diverse scope, in which analysis of data requires evaluation of identifiable factors. Conduct failure investigation with cross functional teams.
• Following SOPs, ensure accurate and complete complaint handling and documentation in the Complaint Management System.

Required Knowledge, Skills, and Abilities:

• BS/MS in Science, Clinical Laboratory Science.
• 5-7 years of industry/ laboratory experience in medical device industry.
• Knowledge and application of computer, MS-Excel, MS-Word, database is a must.
• Bilingual preferred, fluent in English and at least one Asian languages.
• Ability to work independently and in a team environment with multiple cultures, multiple organizations and multiple internal departments.
• Highly organized with demonstrated attention to detail and ability to cut through complex logistics for results.
• Ability to follow complex procedures and processes, and to use good judgment.
• Knowledge of high level concepts of RNA – DNA, and nucleic acid amplification (NAAT).
• Excellent written/verbal communication and organizational skills.
• Experience in technical support, nucleic acid amplification and 4-5 years work in a laboratory.

Additional Data

Preferred Qualifications:

BS/MS in Science, Clinical Laboratory Science.
5-7 years of industry/ laboratory experience in medical device industry.
Experience in technical support, nucleic acid amplification and 4-5 years work in a
laboratory.

Physical Demands:

Support phone and e-mail technical support lines for different shifts. including
weekends and holidays as schedule demands.
Ability to handle phone support for up to 6 hours per day.

CLS Positions - Palo Alto Medical Foundation

We currently have CLS positions open here in Palo Alto. Our lab is a basic core lab: Chemistry, Hematology, Coag and UA.

We would very much appreciate it if you could recommend to us, licensed CLS graduates of your program who are looking for employment.

Michael Lee, M.S., CLS (ASCP)

West Bay PAMF Labs Manager

Palo Alto Medical Foundation

795 El Camino Real

Palo Alto, CA 94301

Telephone:650-853-2806

Fax 650-853-4944

email:leem12@pamf.org

CLS/Research Associate - Aria Diognostics - San Jose, CA

Aria Diagnostics is a privately funded biotechnology company developing non-invasive prenatal tests.  The company is utilizing molecular biology techniques to offer pregnant women a better option than current prenatal testing.  Aria Diagnostics plan to develop a simple blood test that provides pregnant women with information on the health of their baby early in pregnancy.  The company is headquartered in San Jose, CA

Position:  Clinical Laboratory Scientist/Research Associate

Overview::

The Clinical Laboratory Scientist/RA is responsible for performing high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures and complying with all applicable local, state and federal laboratory requirements.  The high conplexity nature of the work requires excellent attention to detail effective written and verbal communication skills, the ability to multi-task and be flexible with tasks and schedules and the ability to work independently in a team environment.

Principal responsibilities include:

• Perform laboratory tests, procedures and analyses according to the laboratory's standard operating procedures
• Perform, review and document laboratory quality control procedures
• Operate, maintain and troubleshoot laboratory equipment
• Prepare reagents required for laboratory testing
• Review, interpret and report patient results
• Independently identify and troubleshoot basic problems that adversely affect test performance
• Communicate effectively with coworkers and non-laboratory personnel
• Report all concerns of test quality and/or safety to the Supervisor or Safety Officer
• Assist with final development of protocol and processes for a Laboratory Developed Test and perform other duties as assigned

Requirements:

We seek an individual with a successful track record who must be comfortable with a start-up environment.  The ideal candidate:

• Must possess a valid California CLS license, generalist preferred
• Completion of a CLS training program at an accredited institution or clinical laboratory work experience within the last five years
• Possess working knowledge of local, state and federal laboratory regulations
• Computer skills a must, automation skills preferred
• Ability to analyze and problem solve basic issues that impact test performance
• Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed
• Able to integrate and apply feedback in a professional manner
• Able to manage daily test processing needs with high emphasis on quality
• Ability to work as part of a team
• Ability to perform repetitive tasks
• High volume laboratory experience preferred
• Training in molecular biology techniques preferred

Reporting:  Reports to the Clinical Lab Supervisor

Compensation:  Attractive salary, equity, and benefits package

Please send cover letter and resume to dpuckett@ariadx.com

Various CLS Positions throughout CA - Sutter Health

There are a number of positions available through SutterHealth.  See their job search tool at:

https://sutterhealth.taleo.net/careersection/sh/jobsearch.ftl?lang=en&radiusType=M&radius=1&searchExpanded=true&CFID=150252792&CFTOKEN=67727968&jsessionid=7e3064b980da7e27201cTR

CLS II - Verinata Health, Redwood City, CA

Clinical Laboratory Scientist II (CLS II)

Artemis Health is an early-stage company dedicated to the development of non-invasive prenatal diagnostic tests.
Our mission is to develop diagnostic tests that provide women, their families and healthcare providers with accurate
and timely information about fetal and maternal health. We do this by developing and commercializing non-invasive
and accurate prenatal diagnostic tests for use in early pregnancy, for all women.

Our company is located in Redwood City, CA. We are looking for talented people with proven skills in their discipline
who enjoy working in a collaborative environment to further advances in maternal and fetal health care. This
opportunity to work within a small entrepreneurial team offers tremendous growth opportunities, with competitive
benefits and compensation.

We are seeking a California Clinical Laboratory Scientist (licensed) who is highly motivated to join our efforts in
processing maternal blood and performing genetic analysis.

Responsibilities:

• Responsible for testing and reporting clinical laboratory results used to aide physicians in the diagnosis and treatment of patients
• Selection, implementation, and evaluation of results for Quality Control materials used in statistical process control of laboratory assays
• Troubleshooting assays and equipment for which QC materials fail to perform adequately
• Participation in activities required to support all necessary licensure for the clinical laboratory, including quality management functions and on-site inspections of the laboratory
• Responsibility for maintaining updated understanding and knowledge of the methods employed in the laboratory and the use of the resulting information by physicians through continuing education activities

Requirements:

• B.S. in medical technology, or biological sciences with a curriculum meeting national testing personnel standards
• California Clinical Laboratory Scientist license in categories appropriate for the area of testing performed 
• 2-5 years experience in a clinical laboratory setting involving molecular pathology and/or nucleic acid analysis
• Excellent communication, teamwork player, organizational and time management skills are essential

Interested parties should apply to https://home.eease.com/recruit/?id=535171

Verinata Health, Inc. is an equal opportunity employer.