Saturday, March 21, 2009

Molecular Clinical Lab Scientist - Illumina

Illumina is the only life sciences company developing genome-wide technologies for genotyping, gene expression and sequencing—the three cornerstones of modern genetic analysis. By enabling studies of thousands of patient samples at once, our products set genetic discovery on fast forward. And we’re just getting started.

Molecular Clinical Lab Scientist
Job Responsibilities include but are not limited to: Responsible for performing technical and scientific processes and procedures in a high complexity genetic testing CLIA certified laboratory.

Tasks and Responsibilities:

  • Perform high complexity laboratory tests according to approved policies and procedures for all phases of testing; pre-analytic, analytic, and post-analytic, as well as general laboratory systems.
  • Perform troubleshooting, maintenance and calibration of instrumentation and equipment used to perform the testing.
  • Follow quality control and quality assessment programs.Evaluate test results for completeness, accuracy and quality.
  • Report test results to clients.
  • Assist with revising laboratory documents including policies, procedures, forms.Follow all safety policies and procedures.
  • Other responsibilities as assigned.
  • Manage goals within defined target timeframes, may manage small technical teams to achieve their goals.
  • Perform data analysis and present results.
  • Perform other duties as assigned.

Qualifications:

Preferred Educational Background:
B.S. degree or equivalent in chemistry, biological sciences, or related field with current California CLS license required.

Preferred Experiential Background:
  • 0-1 years experience in a scientific discipline and experience in a CLIA environment preferred.
  • Knowledge of technology development in a fast paced biotech environment.
  • Excellent laboratory, experimental skills.
  • Technically sound; show potential for technical proficiency and scientific creativity
  • Sound understanding of the latest genomics technologies, methodologies, and practices.
  • Basic understanding of optical and robotic systems.
  • Strong data analysis skills, ability to interpret and draw conclusions from vast amounts of data.
  • Knowledge of Microsoft Excel and Outlook required.
  • Good communication and team management skills.
  • Must be very detail oriented.
When you join the high-performing team at Illumina, your work takes on new meaning—to an exponential degree. Our growth, our positive culture, and the impact our products are having in the world ignite a passion that drives our people forward. And together, we accomplish beyond expectations.

Monday, March 16, 2009

Sutter Jobs

CPMC has some positions open. Check it out! You can e-mail me for more info if you need it. You can also contact the recruiter.

Tuesday, February 17, 2009

From a recruiter at "On Assignment"

Clinical Laboratory Scientist (CLS)
Interested candidates please send an email with “CLS Scientist” in the subject to tina.pham@onassignment.com

Summary : We have an opportunity for a Clinical Laboratory Scientist (CLS) on our dynamic team. This individual would be responsible for performing pre-analytical, analytical and post-analytical procedures. In this position, the Clinical Laboratory Scientist would be working directly under the laboratory director.
Major Duties and Responsibilities:
• Maintain equipment and instruments in good operating condition, recognize any malfunctions and troubleshoot as needed.
• Verify the proper specimen being analyzed for patients and perform correct tests that need to be completed.
• Analyze clinical laboratory specimens following the standard methods and procedures
• Performs quality control procedures to ensure accuracy of clinical data
• Complete routine preventive maintenance and troubleshooting on instruments and equipment
• Responsible for maintaining updated understanding and knowledge of the methods employed in the laboratory
• May work with Development on new projects.
• Working with the manager will monitor and ensure implementation of goals to meet established quality assurance, quality control, and quality improvement plans.
• Ensures compliance with all regulatory agency requirements through documentation, audits, and corrective action.
• Perform Quality Control tests on new incoming shipments of raw materials
• Participates in the updating of departmental standard operating procedures and database to accurately reflect the current practices.
• Performs other tasks as specified by the manage/director. Education/Experience

Requirements:
• Current California Clinical Laboratory Scientist (CLS) license.
• Minimum of 2-4 years of experience as a CLS or equivalent in a clinical laboratory environment.
• BS/BA degree in Medical Technology or related field
• Must have proven interpersonal, communication, computer, and technical skills.
• Molecular diagnostic experience a must.
• Excellent oral and written communication skills required.
• Word processing, statistical/data management skills required.


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Laboratory Supervisor, Clinical Laboratory Scientist (CLS)
Interested candidates please send an email with “CLS Lab Supervisor” in the subject to tina.pham@onassignment.com

Summary: We have an opportunity for a Laboratory Supervisor CLS on our dynamic team. Under direction of the manager/director plans, organizes, schedules, and directs work in order to effectively maximize employee, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. This individual will provide direct on-site supervision of specimen workflow, test performance, quality, compliance, and associated documentation to adhere to the department and company policies and procedures. Responsibility will also include technical support to laboratories running our in vitro diagnostic (IVD) test both by phone and in person.

Major Duties and Responsibilities:
• Responsible for the day-to-day operations of the laboratory. In conjunction with the Laboratory Manager, ensures all departmental policies and procedures meet the standards of current state, federal and CLIA regulations.
• Maintains adequate staffing by interviewing, hiring, training, and assessment of personnel.
• Performs the scheduling, planning, staffing, and monitoring of workflow to meet established goals.
• Supports, implements, and ensures compliance with all department and company policies and procedures.
• Provides staff development through performance development and review and corrective counseling.
• Procures appropriate supplies and equipment to maximize department efficiency and meet established budgetary and quality goals.
• Provides technical oversight of area(s) of responsibility and serves as a technical resource for problem solving and process improvement to ensure accurate test performance.
• Devotes time to direct specimen testing/troubleshooting as needed to maintain adequate workflow.
• Uses effective two-way communication in leading/participating in general laboratory meetings.
• Maintain equipment and instruments in good operating condition, recognize any malfunctions and troubleshoot as needed.
• May work with Development on new projects.
• Working with the manager/director will monitor and ensure implementation of goals to meet established quality assurance, quality control, and quality improvement plans.
• Ensures compliance with all regulatory agency requirements through documentation, audits, and corrective action.
• Participates in the updating of departmental standard operating procedures and database to accurately reflect the current practices.
• Participates in supervisory skills training.
• Travel may be required up to 10% of time
• Performs other tasks as specified by the manage/director. Education/Experience

Requirements:
• Current State of California Clinical Laboratory Scientist license.
• Minimum of 6 years of experience as a medical technologist or equivalent in a clinical laboratory environment to include a supervisory function.
• BS/BA degree in Medical Technology or related field
• Must have proven leadership, interpersonal, communication, computer, and technical skills.
• Molecular diagnostic experience a must.
• Excellent oral and written communication skills required.
• Word processing, statistical/data management skills required.

Friday, January 30, 2009

Gene Security Network

Gene Security Network, Inc. (GSN) is a new company applying a novel preimplantation genetic diagnosis technology to help parents select the healthiest embryos during IVF. With commercial release of its first product and recent CLIA certification, GSN is seeking a motivated and skilled full-time clinical laboratory scientist.

This individual must have a current ASCP medical technologist license with experience in Chemistry or Genetics. The shift will be a "late swing" shift, i.e., 7pm to 3am and will involve advanced protocols using single cell molecular technology and high-throughput DNA microarrays. Ideally this individual will also help with validation of new protocols for submission to Laboratory Field Services for approval under CLIA as well as for potential IVD submissions to the FDA. This position will also involve work related to quality assurance and proficiency testing, as well as equipment maintenance and sample tracking. Experience with PCR, DNA extraction, and/or DNA microarrays is preferred but not required.

Please contact Dr. David Johnson, Director of Research Development, at 650-249-9090x308 or djohnson_at_genesecurity.net.

Rumors and Reports

Berkeley Heart Labs: Says they are looking for people - technician and CLS level

Hunter Labs: May be looking for people to do molecular testing (call Judy Fusco)

K.A. Recruiting

Dear Soon-to-be Graduates and Alumni,

If you are looking for a great job opportunity now or may be looking for a new job opportunity in the future, please contact K.A. Recruiting. At no cost to candidates we will find you the perfect job for after you graduate. We work with many clients across the country – from hospitals, to clinics, to labs, to private practices, to non-profits, to large corporations. We have clients across the country in every setting. We place candidates in entry-level positions, management positions, and executive level positions – depending on their experience level. If you are interested in discussing your career with us, looking for a new job, getting assistance on your resume, or you need help with interview preparation, we can help you.
Below are some current opportunities as of January 30th, 2009. Due to the number of opportunities we have available, we cannot list all of them. However, please give us a call or send us an email to find out about opportunities close to you.

MT/MLT/CLS openings: OR, ME, CA, OH, CO, FL, VA, NY, NJ, TX
HT/HTL openings: GA, NY, NJ, CA, MN, CT, PA, KY
Lab Supervisor openings: OK, NJ, NY, MA
Lab Management openings: NC, OH, AZ
Blood Bank Openings: NJ, NY, TN, GA, OH, WA
Microbiology Openings: CT, AZ, FL, PA, NY, NJ, CT, CA, OR
Molecular Diagnostic Openings: CA

If you do not see an opportunity you are interested in, please contact us. We have hundreds of positions currently available. Our contact information is below.

Sincerely,

Alisha R. Taylor, Founder
K.A. Recruiting, Inc.
www.ka-recruiting.com
Phone: 617-342-8260
Email: Alisha@ka-recruiting.com

Thursday, January 22, 2009

General Supervisor, Molecular Diagnostics

CLIA Laboratory General Supervisor
Location: San Francisco/South Bay Area, CA US
Job Type: Full Time
Job Level: Senior
Education: Bachelors Degree or Equivalent
Category: Clinical Development

Growing oncology medical device diagnostic company located near San Jose,CA. Company has under 100 employees and position is open due to growth.

Position Summary We currently have a key assignment available for a proven leader to takeresponsibility for the set up, certification and technical and scientificperformance of our high complexity genetic testing CLIA certifiedlaboratory. We'll rely on you to directly manage the personnel and dailyoperations of the lab, including coordinating technical/administrativefunctions, supervising high complexity testing personnel, implementing andmaintaining a Quality Management System, verifying test systems andestablishing a robust program for troubleshooting, maintenance andcalibration of instrumentation and equipment. You will also be expected tomaintain an approved Proficiency Testing program, QC/QA programs and anapproved procedure manual, as well as evaluate test results.

Requirements To qualify, you must have 7+ years of related experience, including 3 yearsof hands-on management supervisory experience, a California CLS or CGMBlicense and meet the requirements for General Supervisor and TechnicalSupervisor under CLIA regulations (42CFR, part 493). A BS in Chemistry or abiological science and knowledge of molecular biology or medical geneticsare preferred. Experience in a high complexity CLIA/CASP environment isstrongly preferred and an advanced degree along with experience with DNAisolation, PCR, genotyping technologies, robotics and LIMS systems would bea plus.Please send your CV to karline@crimsonsearch.com