Molecular Technologist II: Tuesday - Saturday (3:00PM - 11:30PM)

Foundation Medicine

3d•Onsite

About The Position

The Molecular Technologist II is a key member of clinical diagnostic laboratory operations, performing complex patient sample testing, solution and reagent preparation, equipment maintenance, and other tasks related to handling and testing patient specimens. The role is cross-functionally trained to perform multiple process steps and/or assays and may provide on-the-job training to colleagues. This regulated position requires regular work in the presence of chemicals and reagents. Molecular Technologists are assigned to one of three shifts and may be assigned to work any day the laboratory is operational. Regular onsite work at a designated Foundation Medicine location is an essential function of the role. Additional information about qualifications under applicable regulatory guidelines may be available from Quality Assurance. The expected salary range for the primary location of Boston, MA is $62,960–$78,700 per year. A discretionary annual bonus may be available based on individual and company performance. The position qualifies for Foundation Medicine benefits.

Requirements

Bachelor of Science degree in a chemical, physical, biological, or life science.
Certifications or licensure required by the state or county in which the job is posted.
At least 2 years of molecular work experience in a CAP/CLIA-regulated laboratory.
Ability to work in the presence of chemicals and reagents in a laboratory environment.
Agreement to maintain confidentiality regarding sensitive company, employee, and proprietary data and information.
Understanding of HIPAA and the importance of patient data privacy.
Commitment to reflect Foundation Medicine's values of Integrity, Courage, and Passion.
Ability to work well under pressure while maintaining a professional demeanor, both independently and as part of a team.
Ability to prioritize and thoroughly follow up on assigned tasks.
Ability to handle multiple tasks at once and work in a fast-paced environment.
Ability to adapt to changing procedures, policies, and work environments.

Nice To Haves

Molecular Biology American Society of Clinical Pathology (MB-ASCP) certification.
Experience in a Quality System Regulations (QSR)-compliant laboratory.
Familiarity with or experience in DNA manipulation techniques, enzymatic reactions, and sequencing chemistry.
Familiarity with high-throughput platforms and common molecular laboratory equipment, such as pipettes, thermocyclers, and liquid handlers.
Experience with a Laboratory Information Management System (LIMS).
Experience ensuring and maintaining laboratory integrity and quality in sample processing, equipment maintenance, and SOPs.
Proficiency with Microsoft Office Suite, especially Excel and PowerPoint.
Knowledge of laboratory safety protocols.
Strong written and oral communication, collaboration, and problem-solving skills when working with other departments and colleagues.
Strong organization and attention to detail.

Responsibilities

Perform patient sample testing in accordance with established standard operating procedures (SOPs).
Carry out testing workflows while maintaining quality, thoroughness, and optimum result turnaround efficiency.
Extract and isolate nucleic acids.
Prepare Next Generation Sequencing (NGS) libraries.
Execute hybridization and genetic sequencing methods.
Process samples using automated 8-span and 96-head liquid-handling platforms.
Operate quantification, sizing, and NGS instruments.
Use the Laboratory Information Management System (LIMS) to track and execute sample processing.
Perform daily, weekly, monthly, and as-needed equipment maintenance checks.
Document process steps and maintain test-result records and data in accordance with Good Documentation Practices (GDP).
Document and assist with investigations of non-compliance events through NCRs, CAPAs, and related processes.
Participate in continuous quality improvement activities.
Review SOPs at set intervals and sign to document knowledge of the procedures.
Collaborate on SOP revisions and drafts as needed for process improvement initiatives and regulatory changes.
Train colleagues in laboratory processes.
Participate in reagent and assay quality control and validations.
Monitor and communicate supply and reagent inventory needs as inventory diminishes.
Perform other duties and projects pertinent to the level of expertise, as assigned.
Comply with Foundation Medicine's attendance policies.