6,125 Quality Control Trainee jobs in the United States

Responsibilities

Join the leading beverage provider, Reyes Coca-Cola Bottling!

* Shift: Full Time, 2nd Shift, 1:30pm start, some weekends
* Benefits: Medical, Dental, Vision, 401K Match, PTO, Education Reimbursement
* Hiring Bonus: $3,000

If you enjoy our products, you'll really enjoy being a part of our team!

Position Responsibilities:

* The QA/QC Supervisor maintains corporate and franchise partner standards as well as environmental health and safety standards establishing operational procedures in collaboration with quality assurance manager


* This role ensures that all work assessments and activities are in accordance with policies of the company, focusing on removing costs, continuous improvement, and removing inefficiencies


* You will direct quality assurance employees in a Manufacturing facility ensuring that all QA equipment is in excellent operating order


* Other duties as assigned



Qualifications

Required Education and Experience:

* Associate's Degree with 4 plus years of related experience and 0 to 1 plus years of supervisory experience or High School Diploma/General Education Diploma with 6 plus years of related experience and 1 to 2 plus years of supervisory experience



Preferred Education and Experience:

* Bachelor's degree



Essential Information for Our Employees

At the Reyes Family of Businesses, our Total Rewards Strategy prioritizes the holistic well-being of our employees, and our compensation philosophy embraces diverse factors for fair pay decisions, valuing skills, experience, and the needs of our business. Company policy prohibits discrimination and harassment against any applicant or employee based on any status or basis protected by applicable law. In addition, the Company is committed to providing reasonable accommodation to applicants and employees in accordance with applicable law. Please note, if you are an employee in the US moving from one position to another, you may be subject to additional background screening based on the requirements of the new role.

Join the leading beverage provider, Reyes Coca-Cola Bottling!
+ Shift: Full Time, 2nd Shift, 1:30pm start, some weekends
+ Benefits: Medical, Dental, Vision, 401K Match, PTO, Education Reimbursement
+ Hiring Bonus: $3,000
If you enjoy our products, you'll really enjoy being a part of our team!
Position Responsibilities:  
+ The QA/QC Supervisor maintains corporate and franchise partner standards as well as environmental health and safety standards establishing operational procedures in collaboration with quality assurance manager
+ This role ensures that all work assessments and activities are in accordance with policies of the company, focusing on removing costs, continuous improvement, and removing inefficiencies
+ You will direct quality assurance employees in a Manufacturing facility ensuring that all QA equipment is in excellent operating order
+ Other duties as assigned
Required Education and Experience:  
+ Associate's Degree with 4 plus years of related experience and 0 to 1 plus years of supervisory experience or High School Diploma/General Education Diploma with 6 plus years of related experience and 1 to 2 plus years of supervisory experience
Preferred Education and Experience:  
+ Bachelor's degree
Benefits
At the Reyes Family of Businesses, our Total Rewards Strategy prioritizes the holistic well-being of our employees. This position offers a comprehensive benefits package that includes Medical, Dental, Vision coverage, Paid Time Off, Retirement Benefits, and complimentary Health Screenings.
Equal Opportunity Employee & Physical Demands
Reyes Holdings and its businesses are equal opportunity employers. Company policy prohibits discrimination and harassment against any applicant or employee based on race, color, religion, sex, pregnancy or pregnancy-related medical conditions, marital status, sexual orientation, gender identity or expression, age, national origin, citizenship, disability, genetic information, military or veteran status, or any other basis protected by applicable law. In addition, the Company is committed to providing reasonable accommodation to applicants and employees in accordance with applicable law. Requests for accommodation should be directed to your point of contact in the Talent Acquisition or Human Resources departments.
Background Check and Drug Screening
Offers of employment are contingent upon successful completion of a background check and drug screening.
Pay Transparency
Our compensation philosophy embraces diverse factors for fair pay decisions, valuing skills, experience, and the needs of our business. Moreover, this role may have the opportunity to participate in a discretionary incentive program, subject to program rules.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation and gender identity, national origin, disability, or protected veteran status. Drug Free Workplace.

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Leica Biosystems, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we're transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact.

Learn about the Danaher Business System which makes everything possible.

The Manager, Quality Assurance and Quality Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material inspection program, QA product release, nonconformance workflows, CDT&R, and calibration.

This position reports to the Director, Quality Assurance and Regulatory Compliance responsible for ensuring that the business, product, and processes meet all Quality and Regulatory standards and requirements. This position is part of the Quality Assurance and Regulatory Compliance department located in Richmond, Illinois and will be onsite.

In this role, you will have the opportunity to:

* Hire, develop, engage, and retain highly capable QA and QC team members, ensuring that each associate is meeting performance requirements and that each critical position has an identified successor with a targeted and robust development plan.
* Oversee inspection and product release activities as well as CDT&R, and develop key strategies to support future business success.
* Coach the team on how to effectively manage and anticipate changing needs for resources and how to flex resource allocation in the face of changing circumstances, including notifying stakeholders and recommending countermeasures to ensure that cross-functional teams and projects are staffed with qualified and skilled QA and QC associates and business needs are met.
* Manage relationships with relevant cross-functional leaders including participating in Daily Management meetings and effectively communicating issues, risks, and needs to the Leadership team.
* Plan, prioritize, and coordinate workflow and cross-site/function interactions to ensure on time delivery of product and projects and compliance with quality systems and standards, using advanced knowledge of Danaher Business System (DBS) tools.
* Ensure site audit readiness at all times through monitoring and learning from past audits, training and preparation of staff and mitigation of risks.
* Support team in formulating and testing effective data-based strategy for winning against the competition or exceeding expectations as a team.

The essential requirements of the job include:

* Bachelor's degree or equivalent advanced degree in engineering, science, medical, or technical field and 5+ years' experience with increasing responsibility in medical device/IVD
* Experience working within a medical device quality system in compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations
* Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues
* Track record of collaborating with technical groups to identify product improvement opportunities

Travel, Motor Vehicle Record & Physical/Environment Requirements:

* Travel requirements <5% of the time, domestic and international
* Overnight travel may be required
* Be able to occasionally lift and/or move up to 40 pounds.
* Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
* This position will occasionally require travel by car and flying in and out of airports with possible long wait times

It would be a plus if you also possess previous experience in:

* Knowledge of lean tools such as 5S, Standard Work, KANBAN, Policy Deployment, Value Stream Management, Visual Management, SAP etc.
* Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies, and understanding of manufacturing processes with high mix low volume and high mix high volume environment.
* Demonstrated ability to lead, develop, communicate, and implement a strategy to ensure compliance to company, regulatory and industry requirements.
* Experience and/or knowledge of NCRs

The annual salary range for this role is $120,000 - $140,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

#LI-GC1

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Leica Biosystems, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we're transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact.

Learn about the Danaher Business System ( which makes everything possible.

The Manager, Quality Assurance and Quality Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material inspection program, QA product release, nonconformance workflows, CDT&R, and calibration.

This position reports to the Director, Quality Assurance and Regulatory Compliance responsible for ensuring that the business, product, and processes meet all Quality and Regulatory standards and requirements. This position is part of the Quality Assurance and Regulatory Compliance department located in Richmond, Illinois and will be onsite.

In this role, you will have the opportunity to:

+ Hire, develop, engage, and retain highly capable QA and QC team members, ensuring that each associate is meeting performance requirements and that each critical position has an identified successor with a targeted and robust development plan.

+ Oversee inspection and product release activities as well as CDT&R, and develop key strategies to support future business success.

+ Coach the team on how to effectively manage and anticipate changing needs for resources and how to flex resource allocation in the face of changing circumstances, including notifying stakeholders and recommending countermeasures to ensure that cross-functional teams and projects are staffed with qualified and skilled QA and QC associates and business needs are met.

+ Manage relationships with relevant cross-functional leaders including participating in Daily Management meetings and effectively communicating issues, risks, and needs to the Leadership team.

+ Plan, prioritize, and coordinate workflow and cross-site/function interactions to ensure on time delivery of product and projects and compliance with quality systems and standards, using advanced knowledge of Danaher Business System (DBS) tools.

+ Ensure site audit readiness at all times through monitoring and learning from past audits, training and preparation of staff and mitigation of risks.

+ Support team in formulating and testing effective data-based strategy for winning against the competition or exceeding expectations as a team.

The essential requirements of the job include:

+ Bachelor's degree or equivalent advanced degree in engineering, science, medical, or technical field and 5+ years' experience with increasing responsibility in medical device/IVD

+ Experience working within a medical device quality system in compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations

+ Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues

+ Track record of collaborating with technical groups to identify product improvement opportunities

Travel, Motor Vehicle Record & Physical/Environment Requirements:

+ Travel requirements <5% of the time, domestic and international

+ Overnight travel may be required

+ Be able to occasionally lift and/or move up to 40 pounds.

+ Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.

+ This position will occasionally require travel by car and flying in and out of airports with possible long wait times

It would be a plus if you also possess previous experience in:

+ Knowledge of lean tools such as 5S, Standard Work, KANBAN, Policy Deployment, Value Stream Management, Visual Management, SAP etc.

+ Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies, and understanding of manufacturing processes with high mix low volume and high mix high volume environment.

+ Demonstrated ability to lead, develop, communicate, and implement a strategy to ensure compliance to company, regulatory and industry requirements.

+ Experience and/or knowledge of NCRs

The annual salary range for this role is $120,000 - $140,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

#LI-GC1

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit .

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here ( .

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .

Division: Dallas Main

Project Location(s): Dallas, TX 75231 USA

Minimum Years Experience: 5 Travel Involved: Job Type: RegularJob Classification: ExperiencedEducation:Job Family:ConstructionCompensation:Salaried Exempt

Position Description: Responsible for planning, coordinating and developing the project-specific Quality Assurance/Quality Control (QA/QC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents. Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff.

Reports to: Project Manager or Project Executive

Essential Duties & Responsibilities*:

* Manage the development and implementation of the project-specific QA/QC Plan in coordination with the project team, the owner/architect team and the contract documents.
* Assure that sufficient, qualified specialized staff is assigned to provide the required knowledge and experience to execute the plan.
* Maintain a collaborative working relationship with owners, architects, consultants, subcontractors and vendors to ensure that the project-specific QA/QC Plan delivers a fully compliant project.
* Lead, supervise and develop all Turner QA/QC staff, including providing input on or completing performance appraisals.
* Ensure strict adherence to ethics and compliance requirements at all times.
* Develop a comprehensive working knowledge and understanding of the contract documents (including Turner's contract, plans, specifications and applicable codes).
* Develop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements.
* Implement project-specific QA/QC Plan in coordination with the project safety plan.
* Understand the project execution plan and coordinate QA/QC procedures at appropriate stages of the work, in line with the project schedule.
* Continually improve strategies and tools to efficiently and effectively document, track and record compliance with the contract documents.
* Execute the project-specific QA/QC Plan in a manner that engages all project staff, subcontractors, vendors and consultants.
* Execute the project-specific QA/QC Plan in a manner that engage all project staff, subcontractors, vendors and consultants.
* Conduct testing and inspections and arrange for third-party testing and inspections. Analyze and report the results.
* Expand the development of the plan as the project progresses as appropriate to expand the project by continually improving procedures.
* Direct removal and replacement of, and document all non-compliant materials and/or workmanship. Document compliance after corrective work is completed prior to starting any subsequent work.
* Research and apply additional QA/QC and Lean procedures to enhance the quality of project delivery.
* Oversight of project close-out and quality reports.

Qualifications: Bachelor's Degree with a minimum of five years' experience or equivalent combination of education, training and/or experience and construction experience that bridges both field and engineering responsibilities. Knowledge of the construction process, means and methods, and materials, their characteristics, installation procedures and tolerances. Strong computer skills and a familiarity with Microsoft Office Suite. Knowledge of Turner's project management software and leadership skills. Very strong verbal and written communication skills are required. Proven leadership qualities and skills with the desire to teach and mentor staff. May require QA/QC certification depending on specific project.

Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and taste or smell. The employee is frequently required to stand and walk. The employee is occasionally required to climb or balance and stoop, kneel, or crouch. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.

Work Environment: While performing the duties of this job, the employee regularly works on-site at the construction work site where the employee is exposed to moving mechanical parts; high precarious places; fumes or airborne particles; outside weather conditions and risk of electrical shock. The noise in these work environments is usually moderate to very loud.

* May perform other duties as assigned.

Turner is an Equal Opportunity Employer - race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by applicable law.

Project located in Altus, OK.
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.

Key Responsibilities

• Develop and implement quality assurance policies and procedures to ensure compliance with ISO standards and regulatory requirements.
• Manage and lead the quality assurance and quality control team to ensure effective testing and quality checks.
• Conduct regular audits of processes and products to identify areas for improvement and ensure adherence to quality standards.
• Oversee the development and execution of testing protocols, including manual and automation testing.
• Utilize root cause analysis to investigate quality issues and implement corrective actions to prevent recurrence.
• Collaborate with cross-functional teams to promote quality awareness and ensure quality practices are integrated into all aspects of production and development.
• Analyze quality data and metrics to identify trends, risks, and opportunities for process improvement.
• Facilitate training sessions for staff on quality standards, documentation, and best practices in quality control.

Qualifications

• Bachelor's degree in Quality Assurance, Engineering, or a related field.
• Minimum of 5 years of experience in quality assurance and quality control roles, with at least 2 years in a management position.
• Strong knowledge of ISO standards and regulatory compliance requirements.
• Proven experience in testing methodologies, including software testing, automation testing, and manual testing.
• Excellent analytical and problem-solving skills with a focus on continuous improvement.
• Strong documentation skills with the ability to create and maintain quality manuals and policies.
• Experience in risk management and root cause analysis.
• Ability to work collaboratively in a team environment and communicate effectively with all levels of the organization.

Benefits

• Full Benefits
• 3 Weeks PTO
• Company vehicle

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Leica Biosystems, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we're transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact.
Learn about the Danaher Business System ( which makes everything possible.
The Manager, Quality Assurance and Quality Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material inspection program, QA product release, nonconformance workflows, CDT&R, and calibration.
This position reports to the Director, Quality Assurance and Regulatory Compliance responsible for ensuring that the business, product, and processes meet all Quality and Regulatory standards and requirements. This position is part of the Quality Assurance and Regulatory Compliance department located in Richmond, Illinois and will be onsite.
In this role, you will have the opportunity to:
+ Hire, develop, engage, and retain highly capable QA and QC team members, ensuring that each associate is meeting performance requirements and that each critical position has an identified successor with a targeted and robust development plan.
+ Oversee inspection and product release activities as well as CDT&R, and develop key strategies to support future business success.
+ Coach the team on how to effectively manage and anticipate changing needs for resources and how to flex resource allocation in the face of changing circumstances, including notifying stakeholders and recommending countermeasures to ensure that cross-functional teams and projects are staffed with qualified and skilled QA and QC associates and business needs are met.
+ Manage relationships with relevant cross-functional leaders including participating in Daily Management meetings and effectively communicating issues, risks, and needs to the Leadership team.
+ Plan, prioritize, and coordinate workflow and cross-site/function interactions to ensure on time delivery of product and projects and compliance with quality systems and standards, using advanced knowledge of Danaher Business System (DBS) tools.
+ Ensure site audit readiness at all times through monitoring and learning from past audits, training and preparation of staff and mitigation of risks.
+ Support team in formulating and testing effective data-based strategy for winning against the competition or exceeding expectations as a team.
The essential requirements of the job include:
+ Bachelor's degree or equivalent advanced degree in engineering, science, medical, or technical field and 5+ years' experience with increasing responsibility in medical device/IVD
+ Experience working within a medical device quality system in compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations
+ Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues
+ Track record of collaborating with technical groups to identify product improvement opportunities
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Travel requirements <5% of the time, domestic and international
+ Overnight travel may be required
+ Be able to occasionally lift and/or move up to 40 pounds.
+ Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
+ This position will occasionally require travel by car and flying in and out of airports with possible long wait times
It would be a plus if you also possess previous experience in:
+ Knowledge of lean tools such as 5S, Standard Work, KANBAN, Policy Deployment, Value Stream Management, Visual Management, SAP etc.
+ Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies, and understanding of manufacturing processes with high mix low volume and high mix high volume environment.
+ Demonstrated ability to lead, develop, communicate, and implement a strategy to ensure compliance to company, regulatory and industry requirements.
+ Experience and/or knowledge of NCRs
The annual salary range for this role is $120,000 - $140,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
#LI-GC1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .