Director, Laboratory Operations Job at Bright Vision Technologies (DeLand)

Laboratory Operations Supervisor

Responsible for the operation of their laboratory area in accordance with establ...

Location

United States , Social Circle

Salary:

86500.00 - 135960.00 USD / Year

BioLife Plasma Services

Expiration Date

Until further notice

Requirements

Have earned a doctoral, master's, or bachelor's degree in a chemical, biological, clinical, or medical laboratory science, or medical technology, or nursing from an accredited institution
Or have earned an associate degree in a chemical, biological, clinical, or medical laboratory science, or medical laboratory technology, or nursing from an accredited institution
Ability to read and follow Standard Operating Procedures (SOPs) and to maintain complete and accurate records
Demonstrate work history of above-average performance and attendance
Excellent interpersonal skills and communication skills, including written, verbal, and oral presentations
Result-oriented with the ability to adapt to changing priorities
Attention to detail and organizational skills with analytical and problem-solving skills
Proficiency in the use of personal computers and software programs, including Microsoft Word, Excel, and PowerPoint
Ability to stand up for 6-8 hours
Ability to lift, carry, and pull up to twenty-five (25) pounds

Job Responsibility

Provides day-to-day supervision of all laboratory operations and moderate or high complexity testing performance in their laboratory area
Functions as a supervisor for testing personnel performing high and moderate complexity testing
Organize and prioritize workloads and assignments in conjunction with donor center requirements
Responsible for maintaining reagent and consumable inventory
Performs annual employee performance reviews and employee counseling
Performs and reviews pre-analytical staff training and competency assessments
Ensures proper training is received under the oversight of the Operations Manager and the CLIA Laboratory Director
Provides technical assistance to staff, operations, and donor centers in laboratory-related issues
Must be accessible to testing personnel at all times testing is performed to provide on-site, telephone, or electronic consultation to resolve technical problems
Performs NCMR, ENC, and CAPA functions

What we offer

Medical, dental, vision insurance
401(k) plan and company match
Short-term and long-term disability coverage
Basic life insurance
Tuition reimbursement program
Paid volunteer time off
Company holidays
Well-being benefits
Up to 80 hours of sick time per calendar year
Up to 120 hours of paid vacation (new hires)

Fulltime

Clinical Laboratory Supervisor - Flow Cytometry

Are you motivated to participate in a dynamic, multi-tasking environment? Do you...

Location

United States , Aliso Viejo

Salary:

99675.20 - 171939.72 USD / Year

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Master of Arts or Master of Science Degree from an accredited institution with a major in one the chemical, physical, or biological sciences, and subsequent to graduation, has had at least four years of pertinent laboratory experience of which not less than two years have been spent working in a clinical laboratory having a director at the doctoral level
Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences with the addition of the successful completion of a course of at least 1 year. At least 6 years of pertinent clinical laboratory experience subsequent to qualifying with 2 of those years spent working in a clinical laboratory with a director at the doctoral level
At least six (6) or more years experience (high complexity testing) preferred in the assigned specialty
At least three (3) or more years of successful experience in a supervisor or leadership capacity preferred
ASCP certification for the assigned specialty, as available
FL: current state supervisor level license to perform laboratory testing
CA: current state supervisor level license to perform laboratory testing
TN: current state supervisor level license to perform laboratory testing

Job Responsibility

Under the direction of, and in the absence of the Laboratory Manager and/or Medical Laboratory Director, the Laboratory supervisor ensures adequate performance of all laboratory procedures
Performs high complexity clinical tests by following department procedures as needed
Presents data and/or information across all levels including the lab, department, division, and corporate, and proficiently answers questions from all groups of staff, managers, and clients
Develops and maintains detailed laboratory procedures manual to meet accreditation and licensing requirements
ensures departmental SOP’s accurately reflects the current process
updates SOP’s as needed
Provides direct supervision of the laboratory operation and personnel performing high complexity testing and reporting of test results by qualified technologists
Initiates and monitors QC programs for the department
assures compliance with regulations
monitors all quality metrics and ensures that corrective actions are documented and implemented

What we offer

Career coaches internally
many training opportunities
highly competitive benefits with a variety of HMO and PPO options
company 401k match
Employee Stock Purchase Program
tuition reimbursement
leadership development
start employees off with 16 days of paid time off plus holidays
wellness courses
highly engaged employee resource groups

Fulltime

Director of Quality

As the Director of Quality, you will be responsible for leading operational qual...

Location

United States , Union City

Salary:

216481.00 - 237601.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

8+ years quality leadership experience in a CLIA-certified laboratory environment with demonstrated ability to lead and manage people and teams
Deep understanding of CLIA, CAP, state laboratory regulations (including NYS Clinical Lab requirements)
Proven track record of successfully reducing quality issues through systematic improvement initiatives
Hands-on experience with supplier quality management, including qualification, auditing, and corrective action management
Experience implementing or optimizing quality processes in a regulated laboratory setting
Strong analytical skills with ability to analyze quality data, identify trends, and develop data-driven solutions
Demonstrated ability to work cross-functionally and influence without direct authority
Ability to work independently and cross-functionally to provide effective updates at executive level
Detail-oriented with well-developed organizational and problem-solving skills
Proven ability to communicate effectively both in writing and verbally with staff at all levels

Job Responsibility

Lead and execute operational quality programs including incident management, material management, supplier management, trending/monitoring, and compliance
Drive continuous improvement initiatives by conducting root cause analyses, implementing corrective actions, and optimizing processes to reduce nonconformances and enhance laboratory efficiency
Partner directly with Lab Operations, Supply Chain, R&D, and other stakeholders to solve problems and embed quality into daily workflows
Serve as subject matter expert for operational quality matters
personally lead critical investigations and improvement projects as needed
Driving systematic reduction of quality issues through root cause analysis, trend identification, and implementation of sustainable corrective actions
Establishing and tracking operational quality metrics (NCR, CAPA, Change Control, Preventive Maintenance, etc.) to drive data-driven decision making
Developing risk-based receiving inspection protocols that balance quality assurance with operational efficiency
Establishing acceptance criteria and sampling plans for incoming materials, reagents, and consumables
Ensuring laboratory quality systems operate effectively to support daily operations

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Accessioner

We are looking for a detail oriented Accessioner to be responsible for assisting...

Location

United States , Union City

Salary:

21.12 USD / Hour

BillionToOne

Expiration Date

Until further notice

Requirements

Student in pursuit of a Bachelor's Biology degree or related life sciences degree
Laboratory experience within the last year preferred
Able to integrate and apply feedback in a professional manner
Strong attention to detail
Able to manage daily specimen processing needs with high emphasis on quality
Able to analyze and problem solve basic issues that impact test performance
Strong computer skills preferred
Able to proactively communicate consistently, clearly, and honestly

Job Responsibility

Perform specimen receipt and accessioning according to the laboratory’s standard operating procedures
Maintain equipment according to the laboratory’s standard operating procedures
Clean labware, equipment, and benches
Prepare documents and binders for equipment and personnel records
Document all corrective actions taken when test systems deviate from the established performance specifications
Perform and document routine preventative maintenance
Prepare reagents required for laboratory preparation
Communicate effectively with coworkers and non- laboratory personnel
Report all concerns of accessioning quality and/or safety to the Laboratory Director, Supervisor, or Safety Officer
Participate in inspection preparation activities

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Free daily on-site lunches provided from top eateries
Latest and greatest hardware (laptop, lab equipment, facilities)
A variety of perks on campus (state of the art gym, restaurant)
Free on-site EV charging (compatible with all EVs, including Tesla)

Fulltime

Associate Director of Operations

The Associate Director of Operations supports and oversees the daily operational...

Location

United States , New York

Salary:

79720.00 - 161199.00 USD / Year

Mount Sinai Health System

Expiration Date

Until further notice

Requirements

Bachelor's degree in public health/administration or business or a related field or equivalent education and experience
Masters (MPA, MPH, MBA or related) is preferred
5 years of experience in a professional business environment
health related and project management experience preferred
Supervisory experience is a plus
1 year in CRO, Pharma, Biotech or ARO preferred

Job Responsibility

Lead all administrative operations, managing a multidisciplinary team supporting clinical trials, registries, and translational research
Provide day-to-day supervision of the Clinical Trial Management Team, Administration Team, and Catheterization Laboratory Research Team
Assist the Director in daily departmental operations and provide professional and administrative guidance to staff
Evaluate operational performance and identify opportunities for improvement
advise and inform the Director of administrative issues, needs, and risks
Plan, organize, and implement services to meet departmental goals and objectives
Develop, implement, and refine departmental policies, procedures, and SOPs to ensure efficiency, quality, and regulatory compliance
Oversee hiring, supervision, mentoring, evaluation, and retention of administrative and research staff
Foster a culture of accountability, inclusivity, collaboration, and professional development
Participate in interviewing and recommending candidates

Quality Assurance Manager - CLIA/CAP Laboratory

10x Genomics is establishing its first CLIA/CAP-certified laboratory to bring cu...

Location

United States , Pleasanton

Salary:

132800.00 - 179600.00 USD / Year

10x Genomics

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Life Sciences, Medical Laboratory Science, Quality Management, or related field
10+ years of experience in quality assurance within a regulated clinical laboratory (CLIA/CAP environment)
Demonstrated experience building or expanding quality systems in a CLIA lab setting
Strong working knowledge of CLIA / CAP quality and documentation requirements
Additional knowledge of FDA 21 CFR Part 820 and ISO 13485 strongly preferred
Experience preparing for and leading CAP inspections and CLIA audits
Excellent written and verbal communication skills, with an ability to collaborate across scientific, operational, and regulatory functions
Hands-on, proactive, and adaptable, capable of working effectively in an early-stage, fast-growing diagnostic environment
Experience with LIMS, electronic QMS tools, and training management systems is required

Job Responsibility

Clinical Quality Framework Establishment and Oversight: Implement document control, deviation/CAPA systems, training programs, and internal audit processes compliant with CLIA, CAP, and applicable state and federal regulations
Collaborate closely with CLIA and assay development teams to develop and manage SOPs and work instructions
Partner with the broader Quality/Regulatory team to integrate the CLIA lab’s quality infrastructure into 10x’s enterprise-wide quality management system (QMS)
Establish and track key quality metrics for laboratory operations (e.g., deviations, nonconformances, complaint handling, audit findings, proficiency testing)
In partnership with CLIA Lab Director, ensure inspection readiness and execute regulatory submissions (CLIA, CAP, and state licensure)
Operational Quality Support: Provide day-to-day quality oversight of clinical laboratory operations, including review and approval of validation plans, QC data, and reports
Serve as QA reviewer/approver for method validation, verification, and change control documentation for both laboratory methods and assay software components
Ensure effective management of reagents, instruments, and workflow changes per CLIA/CAP requirements
Support onboarding and verification of LDTs transferred from Diagnostic Assay Development teams
Act as quality liaison with external auditors and partners

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Generous time off
Competitive and comprehensive health benefits package
Easy-to-use benefits that promote wellbeing
Family friendly policies like parental leave
Award-Winning Workplace

Fulltime

Anatomic Pathology Supervisor

The Anatomic Pathology Supervisor has the overall responsibility for the plannin...

Location

United States , Fort Myers

Salary:

88595.00 - 218658.00 USD / Year

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences with the addition of the successful completion of a course of at least 1 year experience/training/training course in assigned specialty
Master of Arts or Master of Science Degree from an accredited institution with a major in one the chemical, physical, or biological sciences, and subsequent to graduation, has had at least four years of pertinent laboratory experience of which not less than two years have been spent working in a clinical laboratory having a director at the doctoral level
6+ years (in high complexity testing) is preferred in histology laboratory
Experience as a HTL III or Lead Histotechnologist is preferred
Nationally: HT (ASCP) or HTL (ASCP) certification
FL: Current state supervisor level license and state technologist license to perform laboratory testing required

Job Responsibility

Responsible for the day-to-day operations of the Anatomic Pathology laboratory and supervision of the technical and support staff
Initiates and monitors quality control and quality assurance programs for the laboratory
Sets standards, policies, and guidelines for the efficient management of the Anatomic Pathology laboratory
Ensures that the Anatomic Pathology laboratory staff is trained and compliant with Standard Operating Procedures and competency checklists
Oversees, plans, and prepares for inspections
Ensures departmental Standard Operating Procedures accurately reflects the current process
Sets department objectives and performance goals
Drives personnel management activities for the department
Conducts performance appraisals, documenting deficiencies, developing plans for improvement and counsels employees
Monitors laboratory work performance to determine staff resources utilization

What we offer

$10,000 Sign on Bonus
career coaches
many training opportunities
highly competitive benefits with a variety of HMO and PPO options
company 401k match
Employee Stock Purchase Program
tuition reimbursement
leadership development
16 days of paid time off plus holidays
wellness courses

Fulltime

Senior Director of Process Engineering

Are you motivated to participate in a dynamic, multi-tasking environment? Do you...

Location

United States

Salary:

196000.00 - 324000.00 USD / Year

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, Life Sciences, or related field required or equivalent work experience required
Master’s degree preferred
12 or more years of experience in process engineering, laboratory automation, or technology transfer within clinical diagnostics or biotechnology, including 7 or more years in a leadership role required
Ability to travel up to 50% of the time
Proven expertise in technology transfer and laboratory automation
Strong knowledge of Lean Six Sigma and operational excellence methodologies
Experience navigating systems for laboratory workflows, including LIMS
Ability to lead cross-functional teams and manage complex projects
Knowledge of regulatory requirements for clinical laboratories (CLIA, CAP, FDA)
Excellent communication, leadership, and problem-solving skills

Job Responsibility

Provide strategic leadership for engineering projects and initiatives within the laboratory, and manage engineering teams, contractors, and external vendors to ensure on-time, on-budget project delivery
Drive operational excellence through best practices in process optimization, quality, and efficiency
Manage multiple complex projects simultaneously, overseeing resource allocation and providing strategic guidance on priorities
Identify, develop and execute automation strategies that enhance laboratory workflows, reduce turnaround times, and increase reliability in a cost-effective manner
Lead internal and external technology transfer initiatives across all clinical modalities
Identify opportunities for continuous improvement and cost optimization while supporting automation strategies that drive efficiency and scalability, leveraging Lean Six Sigma principles
Collaborate with QA and Compliance teams to ensure all deliverables meet regulatory and quality standards
Ensure compliance with CLIA, CAP, NYSDOH, and other relevant regulations
Apply product development life cycle processes to design and implement new solutions for laboratory operations
Partner with R&D, Lab Operations, QA, and IT to align technology transfer and automation objectives with organizational goals

What we offer

Career coaches internally
Many training opportunities
Highly competitive benefits with a variety HMO and PPO options
Company 401k match
Employee Stock Purchase Program
Tuition reimbursement
Leadership development
Start employees off with 16 days of paid time off plus holidays
Wellness courses
Highly engaged employee resource groups

Fulltime

Director, Laboratory Operations

Bright Vision Technologies

Location:
United States , DeLand

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 31, 2026

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