Ccrps
At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose drivenenvironment. This is what we call the Veracyte way its about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.
Our Values:
We Seek A Better Way : We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
We Make It Happen : We act with urgency, commit to quality, and bring fun to our hard work
We Are Stronger Together :We collaborate openly, seek to understand, and celebrate our wins
We Care Deeply : We embrace our differences, do the right thing, and encourage each other
The Position: Under the general direction of the Laboratory Director, the Laboratory Supervisor is responsible for the day-to-day supervision and oversight of the laboratory operation and personnel performing testing and reporting test results in accordance with the Companys CLIA quality management systems. The Laboratory Supervisor will work closely with and be part of a dynamic, multi-disciplinary team responsible for quality assurance, client services, data management and clinical research.
Essential duties and Responsibilities: The main duties and responsibilities of the Laboratory Supervisor include the following, but not limited to:
Day-to-day supervision of high complexity test performance
Schedule, assign, review, and evaluate the work of laboratory personnel Answer questions and resolve problems raised regarding service or test results
Review quality control of the various procedures performed Direct evaluation and review of new procedures and recommending modifications
Evaluate workload, space, equipment and staffing Interview, select, orient, train and evaluate new employees
Plan, develop, recommend, initiate and implement approved changes in policies, procedures, and methods
Implement operating procedures to comply with State and Federal laws, regulations and standards Investigate questionable test results
Develop procedures, norms, and standards for new laboratory staff Evaluate the level of quality of service and current procedures and methods
Advise staff in difficult tests or special situations Assess the value of new procedures, products, and equipment for utilization by the laboratory
Prepare and justify equipment and personnel budgetary requests Develop, participate in, and attend educational and training programs
Monitor and provide feedback to staff on performance of service standards
Provide support and assistance utilize management principles and teamwork to promote achievement of common goals and to resolve problems
Perform any other site/lab specific duties as assigned
Who You Are: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Education and/or Experience
Active California Department of Public Health Clinical Laboratory Scientist (CLS) license or Clinical Genetic Molecular Biology Scientist (CGMBS) license (no exceptions)
Experience in high complexity clinical laboratory testing, preferably in molecular diagnostics
Performance of molecular testing (PCR, Microarray, Sanger/NGS sequencing) a plus
Has at least 5 years of experience in molecular laboratory that demonstrate proficiency and independence in a clinical laboratory setting
Preferably has experience serving as a General Supervisor, as defined by CLIA
Must have strong analytical and problem-solving skills
Must be detail-oriented and comfortable with technology
Must have excellent verbal and written communication skills
Strong computer skills across diverse platforms
Excellent interpersonal communication and team player attitude Ability to adapt to change and a rapid work pace
Maintains continuing education units required by California Department of Health Services and New York State Department of Health
Physical Requirements
Repetitive movement of hands, arms and leg, fingers (typing and/or writing)
Gripping/grasping
Reaching above/below shoulder level
Sitting, with occasional walking, standing, stooping and moving about
Exposure to general office environment conditions
Occasionally required to lift up to 25 pounds
#LI-Onsite
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Pay range$122,000—$143,000 USD
What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.
About Veracyte Veracyte(Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit www.veracyte.com or follow us on LinkedIn or X (Twitter).
Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View ourCCPA Disclosure Notice.
If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com
PI280398761
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Our Values:
We Seek A Better Way : We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
We Make It Happen : We act with urgency, commit to quality, and bring fun to our hard work
We Are Stronger Together :We collaborate openly, seek to understand, and celebrate our wins
We Care Deeply : We embrace our differences, do the right thing, and encourage each other
The Position: Under the general direction of the Laboratory Director, the Laboratory Supervisor is responsible for the day-to-day supervision and oversight of the laboratory operation and personnel performing testing and reporting test results in accordance with the Companys CLIA quality management systems. The Laboratory Supervisor will work closely with and be part of a dynamic, multi-disciplinary team responsible for quality assurance, client services, data management and clinical research.
Essential duties and Responsibilities: The main duties and responsibilities of the Laboratory Supervisor include the following, but not limited to:
Day-to-day supervision of high complexity test performance
Schedule, assign, review, and evaluate the work of laboratory personnel Answer questions and resolve problems raised regarding service or test results
Review quality control of the various procedures performed Direct evaluation and review of new procedures and recommending modifications
Evaluate workload, space, equipment and staffing Interview, select, orient, train and evaluate new employees
Plan, develop, recommend, initiate and implement approved changes in policies, procedures, and methods
Implement operating procedures to comply with State and Federal laws, regulations and standards Investigate questionable test results
Develop procedures, norms, and standards for new laboratory staff Evaluate the level of quality of service and current procedures and methods
Advise staff in difficult tests or special situations Assess the value of new procedures, products, and equipment for utilization by the laboratory
Prepare and justify equipment and personnel budgetary requests Develop, participate in, and attend educational and training programs
Monitor and provide feedback to staff on performance of service standards
Provide support and assistance utilize management principles and teamwork to promote achievement of common goals and to resolve problems
Perform any other site/lab specific duties as assigned
Who You Are: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Education and/or Experience
Active California Department of Public Health Clinical Laboratory Scientist (CLS) license or Clinical Genetic Molecular Biology Scientist (CGMBS) license (no exceptions)
Experience in high complexity clinical laboratory testing, preferably in molecular diagnostics
Performance of molecular testing (PCR, Microarray, Sanger/NGS sequencing) a plus
Has at least 5 years of experience in molecular laboratory that demonstrate proficiency and independence in a clinical laboratory setting
Preferably has experience serving as a General Supervisor, as defined by CLIA
Must have strong analytical and problem-solving skills
Must be detail-oriented and comfortable with technology
Must have excellent verbal and written communication skills
Strong computer skills across diverse platforms
Excellent interpersonal communication and team player attitude Ability to adapt to change and a rapid work pace
Maintains continuing education units required by California Department of Health Services and New York State Department of Health
Physical Requirements
Repetitive movement of hands, arms and leg, fingers (typing and/or writing)
Gripping/grasping
Reaching above/below shoulder level
Sitting, with occasional walking, standing, stooping and moving about
Exposure to general office environment conditions
Occasionally required to lift up to 25 pounds
#LI-Onsite
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Pay range$122,000—$143,000 USD
What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.
About Veracyte Veracyte(Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit www.veracyte.com or follow us on LinkedIn or X (Twitter).
Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View ourCCPA Disclosure Notice.
If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com
PI280398761
#J-18808-Ljbffr