Supv – Cls
Confirmed live in the last 24 hours
Locations
San Carlos, CA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Requirements
- 2+ years of experience as a Medical Technologist or equivalent in a clinical laboratory environment
- BS/BA degree (or equivalent) in Medical Technology, Biological Sciences, or a related field
- Current MT/MLS/CLS certification preferable from ASCP, AMT, or AAB
- Proven leadership experience
- Able to take on projects with little supervision
- Excellent interpersonal, communication, computer, troubleshooting, and pipetting skills
- Experience in Molecular Biology, GMP, and QSR
- Excellent oral and written communication skills
- Word processing and data management skills
Responsibilities
- Responsible for day-to-day staffing/scheduling/setting up sample run schedules
- Ensures production work is consistently completed according to department goals
- Ensures all case samples are processed and accounted for
- Monitors team members to ensure adherence to SOPs and safety procedures
- Oversees training for new hires: works in conjunction with lead to train new hires
- Document nonconformance reports and all corrective actions taken when test systems deviate from the established performance specifications as needed. Escalates protocol deviation to lead/supervisor
- Assists manager in initiating and completing CAPAs
- Handles employee issues. Collaborates with Manager to resolve issues
- Ensures alignment with team for reasoning behind instructions/processes, changes that are made, why certain ideas cannot be implemented effectively
- Meets regularly with individual team members to discuss goals and progress
- Responsible for staff performance reviews
- Plans and leads shift meetings
- Keeps team morale up and maintains professionalism of team members, including by acting as role model
- Adheres to Departmental Expectations
- Ensures compliance with all regulatory agency requirements through documentation, audits, and corrective action
- Go-to person when manager is not present
- Assists the team in day to day lab work
- Approves timecards and PTO requests
- Escalates lab issues and team concerns to manager. Communicates the problem and suggests possible solutions
- Understands the entire lab process and can identify and troubleshoot issues when they arise
- Understands when and how to escalate issues appropriately
- Makes sure the goals set by manager for the team are being met in the lab
- Performs and completes side projects assigned by the manager
- Actively interacts with interdepartmental teams such as OPS, Accessioning, Extractions, Engineering, Stats, R&D, and Support
- Provides direction to employees according to established policies and management guidance
- Administers company policies that directly affect subordinate employees
- Recommends changes to unit or sub-unit policies
- Provides direct supervision to professional individual contributors and/or skilled, support individual contributors
- Acts as advisor to unit or sub-units and may become actively involved, as required, to meet schedules and resolve problems
- This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job
- Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire
- Must maintain a current status on Natera training requirements
- Performs other duties as assigned
Clinical genetic testing
Company Overview
Natera's mission is to change the management of disease worldwide with a focus on reproductive health, oncology, and organ transplantation.
Benefits
- Flexible medical plans
- Investment options
- Time off
- Workplace perks
Company Core Values
- A person behind every sample
- Embrace diversity
- Be accountable
- Think team
- Learn and nimble
- Show me the data
- Be ready to change the world
- Integrity is in our DNA