Broad Institute of MIT and Harvard
Clinical Laboratory Process Development Associate I
Broad Institute of MIT and Harvard, Burlington, Massachusetts, us, 01805
Clinical Laboratory Process Development Associate I
Join to apply for the
Clinical Laboratory Process Development Associate I
role at
Broad Institute of MIT and Harvard
The Genomics Platform has delivered on transformative projects for more than 30 years. We create foundational genomics resources and capabilities for the community and undertake large-scale disease-based projects that pioneer approaches and advance the understanding of the genomic basis of disease and other traits. We are dedicated to solving the world’s most challenging biomedical problems through the continuous development and investment in cutting edge technology and large‑scale research projects that are both challenging and complex.
Data generated by the Genomics Platform has enabled a wide range of applications, from variant discovery to delivery of polygenic risk scores and clinical diagnoses, and contributed knowledge to a wide array of fields, from rare disease research to population genomics, from cancer clinical trials to understanding cell circuitry.
We are expanding our team to support constantly evolving initiatives at our new, state‑of‑the‑art facility located at 27 Blue Sky Drive, Burlington, MA.
The
Clinical Laboratory Process Development Associate (PDA)
will be committed to carrying out innovative, high‑throughput lab processes and supporting the highest quality research to realize the full promise of genomic medicine. Process Development Associates I (PDA I) are responsible for processing samples through a high‑throughput clinical diagnostics laboratory and meeting production goals. PDAs will function as the regulatory equivalent of clinical laboratory technical personnel (i.e. medical technologists). PDAs will be trained to perform clinical laboratory tests under general supervision. In addition to standard production processes, this position will require individuals to participate in continuous improvement solutions through appropriate change‑management procedures and troubleshooting processes as needed.
The individual may be involved with the design and execution of development, process improvement, or troubleshooting projects under direct guidance from the supervisor in support of platform goals and may be required to complete related training in JMP, Six Sigma, or other process‑improvement methods. Upon completion of these projects the individual is responsible for documenting and communicating results to others in the Platform during dedicated meetings.
In addition, PDAs will assist with the general supervision of the work of other laboratory personnel such as Process Development Technicians and Accessioning Technicians as required.
Primary Responsibilities
Follow standard operating procedures.
Perform only those high‑complexity tests that are authorized by the Laboratory Director and require a degree of skill commensurate with the individual’s education, training, experience, and technical abilities.
Exercise independent judgment and responsibility with minimal supervision by the laboratory director or supervisor.
Adhere to the laboratory’s quality control policies and document all quality control activities, instrument and procedural calibrations, and maintenance performed.
Follow the laboratory’s established policies and procedures whenever test systems are not within the laboratory’s established acceptable levels of performance.
Be capable of identifying problems that may adversely affect test performance or reporting of test results, correct the problems according to procedures or immediately notify the General Supervisor, Technical Supervisor, Clinical Consultant or Laboratory Director.
Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications.
Review and monitor quality metrics and communicate results to others in the Platform during dedicated meetings as needed.
Minimum Qualifications
BS/BA degree in Biology or Chemistry. Please be prepared to provide a copy of the diploma and transcripts upon request.
1+ years of relevant full‑time clinical laboratory experience in this specialty subsequent to obtaining a B.S./B.A. degree.
Solid knowledge of primary biological science principles.
Recent (within the last year) laboratory experience with the use of standard lab equipment such as pipettes and centrifuges.
Strong analytical skills, problem‑solving ability, and innovation aptitude.
Working knowledge of computers, databases, and working in a Windows/Mac environment.
Required Skills and Attributes
Strong attention to detail, the ability to multi‑task, and strong organizational skills.
Follow Standard Operating Procedures and policies.
Excellent written, oral communication skills, interpersonal skills, and ability to work effectively as part of a team.
Ability to work independently with minimal supervision.
Thrives in a fast‑paced environment.
Preferred Experience
Experience with RNA and/or DNA extraction and library construction.
Experience with genomic sequencing.
Experience with laboratory automation.
Data accessioning experience.
Pay Range: $58,000 – $76,667 USD per annum.
Benefits include medical, dental, vision, life, and disability insurance; a 401(k) retirement plan; flexible spending and health savings accounts; at least 13 paid holidays; winter closure; paid time off; parental and family care leave; and an employee assistance program, among other Broad benefits.
The Broad Institute is an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, disability, protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.
Should you need a reasonable accommodation to complete the application or interview process, please contact recruiting@broadinstitute.org for assistance.
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Clinical Laboratory Process Development Associate I
role at
Broad Institute of MIT and Harvard
The Genomics Platform has delivered on transformative projects for more than 30 years. We create foundational genomics resources and capabilities for the community and undertake large-scale disease-based projects that pioneer approaches and advance the understanding of the genomic basis of disease and other traits. We are dedicated to solving the world’s most challenging biomedical problems through the continuous development and investment in cutting edge technology and large‑scale research projects that are both challenging and complex.
Data generated by the Genomics Platform has enabled a wide range of applications, from variant discovery to delivery of polygenic risk scores and clinical diagnoses, and contributed knowledge to a wide array of fields, from rare disease research to population genomics, from cancer clinical trials to understanding cell circuitry.
We are expanding our team to support constantly evolving initiatives at our new, state‑of‑the‑art facility located at 27 Blue Sky Drive, Burlington, MA.
The
Clinical Laboratory Process Development Associate (PDA)
will be committed to carrying out innovative, high‑throughput lab processes and supporting the highest quality research to realize the full promise of genomic medicine. Process Development Associates I (PDA I) are responsible for processing samples through a high‑throughput clinical diagnostics laboratory and meeting production goals. PDAs will function as the regulatory equivalent of clinical laboratory technical personnel (i.e. medical technologists). PDAs will be trained to perform clinical laboratory tests under general supervision. In addition to standard production processes, this position will require individuals to participate in continuous improvement solutions through appropriate change‑management procedures and troubleshooting processes as needed.
The individual may be involved with the design and execution of development, process improvement, or troubleshooting projects under direct guidance from the supervisor in support of platform goals and may be required to complete related training in JMP, Six Sigma, or other process‑improvement methods. Upon completion of these projects the individual is responsible for documenting and communicating results to others in the Platform during dedicated meetings.
In addition, PDAs will assist with the general supervision of the work of other laboratory personnel such as Process Development Technicians and Accessioning Technicians as required.
Primary Responsibilities
Follow standard operating procedures.
Perform only those high‑complexity tests that are authorized by the Laboratory Director and require a degree of skill commensurate with the individual’s education, training, experience, and technical abilities.
Exercise independent judgment and responsibility with minimal supervision by the laboratory director or supervisor.
Adhere to the laboratory’s quality control policies and document all quality control activities, instrument and procedural calibrations, and maintenance performed.
Follow the laboratory’s established policies and procedures whenever test systems are not within the laboratory’s established acceptable levels of performance.
Be capable of identifying problems that may adversely affect test performance or reporting of test results, correct the problems according to procedures or immediately notify the General Supervisor, Technical Supervisor, Clinical Consultant or Laboratory Director.
Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications.
Review and monitor quality metrics and communicate results to others in the Platform during dedicated meetings as needed.
Minimum Qualifications
BS/BA degree in Biology or Chemistry. Please be prepared to provide a copy of the diploma and transcripts upon request.
1+ years of relevant full‑time clinical laboratory experience in this specialty subsequent to obtaining a B.S./B.A. degree.
Solid knowledge of primary biological science principles.
Recent (within the last year) laboratory experience with the use of standard lab equipment such as pipettes and centrifuges.
Strong analytical skills, problem‑solving ability, and innovation aptitude.
Working knowledge of computers, databases, and working in a Windows/Mac environment.
Required Skills and Attributes
Strong attention to detail, the ability to multi‑task, and strong organizational skills.
Follow Standard Operating Procedures and policies.
Excellent written, oral communication skills, interpersonal skills, and ability to work effectively as part of a team.
Ability to work independently with minimal supervision.
Thrives in a fast‑paced environment.
Preferred Experience
Experience with RNA and/or DNA extraction and library construction.
Experience with genomic sequencing.
Experience with laboratory automation.
Data accessioning experience.
Pay Range: $58,000 – $76,667 USD per annum.
Benefits include medical, dental, vision, life, and disability insurance; a 401(k) retirement plan; flexible spending and health savings accounts; at least 13 paid holidays; winter closure; paid time off; parental and family care leave; and an employee assistance program, among other Broad benefits.
The Broad Institute is an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, disability, protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.
Should you need a reasonable accommodation to complete the application or interview process, please contact recruiting@broadinstitute.org for assistance.
#J-18808-Ljbffr