Responsible for managing the overall Quality Assurance function at AngioDynamics Israel. This ... Ensure compliance with all relevant Regulatory, International standards, and legal requirements.
Responsible for managing the overall Quality Assurance function at AngioDynamics Israel. This ... Ensure compliance with all relevant Regulatory, International standards, and legal requirements.
International Quality Assurance Manager (Quality Management Systems)
Worcester, MA · On-site
$121K - $152K/yr
Responsible for managing the overall Quality Assurance function at AngioDynamics Israel. This ... Ensure compliance with all relevant Regulatory, International standards, and legal requirements.
International Quality Assurance Manager (Quality Management Systems)
Worcester, MA · On-site
$121K - $152K/yr
Responsible for managing the overall Quality Assurance function at AngioDynamics Israel. This ... Ensure compliance with all relevant Regulatory, International standards, and legal requirements.
In this dynamic role, you will apply a risk-based approach to Quality Assurance using our Critical ... You look for opportunities to develop your skills within an international team and are passionate ...
In this dynamic role, you will apply a risk-based approach to Quality Assurance using our Critical ... You look for opportunities to develop your skills within an international team and are passionate ...
Quality Assurance Manager
Santa Maria, CA · On-site
$25 - $35/hr
We are seeking a Quality Assurance Manager with a minimum of 5 years of experience in a high ... Ensure products meet international quality standards (ISO9001 and AS9100). * Systems Management:
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Quality Assurance Manager
Santa Maria, CA · On-site
$25 - $35/hr
We are seeking a Quality Assurance Manager with a minimum of 5 years of experience in a high ... Ensure products meet international quality standards (ISO9001 and AS9100). * Systems Management:
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Quality Assurance Manager
San Luis Obispo, CA · On-site
$25 - $35/hr
We are seeking a Quality Assurance Manager with a minimum of 5 years of experience in a high ... Ensure products meet international quality standards (ISO9001 and AS9100). * Systems Management:
Quick apply
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Quality Assurance Manager
San Luis Obispo, CA · On-site
$25 - $35/hr
We are seeking a Quality Assurance Manager with a minimum of 5 years of experience in a high ... Ensure products meet international quality standards (ISO9001 and AS9100). * Systems Management:
QA/RA Specialist
Charlotte, NC · On-site
$75K - $85K/yr
The QA/RA Coordinator ensures products and processes meet quality standards (QA) and regulatory ... or international quality certifications, specifically JACHO and Medicare/Medicaid Standards.
QA/RA Specialist
Charlotte, NC · On-site
$75K - $85K/yr
The QA/RA Coordinator ensures products and processes meet quality standards (QA) and regulatory ... or international quality certifications, specifically JACHO and Medicare/Medicaid Standards.
Develop written procedures for quality control/quality assurance Supervise construction works ... international quality norms/rule/regulations. They supervise working of quality service providers ...
Develop written procedures for quality control/quality assurance Supervise construction works ... international quality norms/rule/regulations. They supervise working of quality service providers ...
QA/RA Specialist
$75K - $85K/yr
The QA/RA Specialist ensures products and processes meet quality standards (QA) and regulatory ... or international quality certifications, specifically JACHO and Medicare/Medicaid Standards.
QA/RA Specialist
$75K - $85K/yr
The QA/RA Specialist ensures products and processes meet quality standards (QA) and regulatory ... or international quality certifications, specifically JACHO and Medicare/Medicaid Standards.
QA/QC Engineer
Houston, TX · On-site
* Develop written procedures for quality control/quality assurance * Supervise construction works ... following national/international quality norms/rule/regulations. * They supervise working of ...
QA/QC Engineer
Houston, TX · On-site
* Develop written procedures for quality control/quality assurance * Supervise construction works ... following national/international quality norms/rule/regulations. * They supervise working of ...
We are seeking a Quality Assurance Technician to help maintain and evolve our Quality Management ... In this role, you will move beyond the workbench to ensure our processes meet international ...
We are seeking a Quality Assurance Technician to help maintain and evolve our Quality Management ... In this role, you will move beyond the workbench to ensure our processes meet international ...
Quality Assurance Technician
Warren, OH · On-site
We are seeking a Quality Assurance Technician to help maintain and evolve our Quality Management ... In this role, you will move beyond the workbench to ensure our processes meet international ...
Quality Assurance Technician
Warren, OH · On-site
We are seeking a Quality Assurance Technician to help maintain and evolve our Quality Management ... In this role, you will move beyond the workbench to ensure our processes meet international ...
Senior QA Manager
Atlanta, GA · On-site
Senior QA Manager Location: Atlanta, GA Position Type: 5 days Onsite Exempt Position * Manage and ... Working knowledge of FDA 21 CFR Part 820, ISO 13485, and other applicable international quality ...
Senior QA Manager
Atlanta, GA · On-site
Senior QA Manager Location: Atlanta, GA Position Type: 5 days Onsite Exempt Position * Manage and ... Working knowledge of FDA 21 CFR Part 820, ISO 13485, and other applicable international quality ...
Senior QA Manager Location: Atlanta, GA Position Type: 5 days Onsite Exempt Position * Manage and ... Working knowledge of FDA 21 CFR Part 820, ISO 13485, and other applicable international quality ...
Senior QA Manager Location: Atlanta, GA Position Type: 5 days Onsite Exempt Position * Manage and ... Working knowledge of FDA 21 CFR Part 820, ISO 13485, and other applicable international quality ...
Senior QA Manager
Atlanta, GA · On-site
Senior QA Manager Location: Atlanta, GA Position Type: 5 days Onsite Exempt Position * Manage and ... Working knowledge of FDA 21 CFR Part 820, ISO 13485, and other applicable international quality ...
Quick apply
Senior QA Manager
Atlanta, GA · On-site
Senior QA Manager Location: Atlanta, GA Position Type: 5 days Onsite Exempt Position * Manage and ... Working knowledge of FDA 21 CFR Part 820, ISO 13485, and other applicable international quality ...
Qa Specialist II- Validation
Bedford, NH · On-site
Quality Assurance Reporting To: QA Manager/QA Director Responsible For (Staff): No The QA ... Keen understanding of international quality systems regulations to adopt best in class systems ...
Qa Specialist II- Validation
Bedford, NH · On-site
Quality Assurance Reporting To: QA Manager/QA Director Responsible For (Staff): No The QA ... Keen understanding of international quality systems regulations to adopt best in class systems ...
Qa Specialist II- Validation
Bedford, NH · On-site
Quality Assurance Reporting To: QA Manager/QA Director Responsible For (Staff): No The QA ... Keen understanding of international quality systems regulations to adopt best in class systems ...
Qa Specialist II- Validation
Bedford, NH · On-site
Quality Assurance Reporting To: QA Manager/QA Director Responsible For (Staff): No The QA ... Keen understanding of international quality systems regulations to adopt best in class systems ...
Manager, Quality Assurance
Phillipsburg, NJ · On-site
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Manager, Quality Assurance
Phillipsburg, NJ · On-site
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Manager, Quality Assurance
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Manager, Quality Assurance
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Manager, Quality Assurance
Phillipsburg, NJ · On-site
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Manager, Quality Assurance
Phillipsburg, NJ · On-site
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Manager, Quality Assurance
Phillipsburg, NJ · On-site
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Manager, Quality Assurance
Phillipsburg, NJ · On-site
$97K - $156K/yr
The QA Manager will provide support and guidance to Quality Assurance associates. Advises ... Strong knowledge of FDA and international Quality System rules and regulations * Strong oral and ...
Temp International Qa information
See salary details
$10.82 - $16.48
4% of jobs
$16.48 - $22.14
12% of jobs
$22.14 - $27.80
7% of jobs
$30.27 is the 25th percentile. Wages below this are outliers.
$27.80 - $33.46
4% of jobs
$33.46 - $39.12
6% of jobs
$39.12 - $44.78
7% of jobs
The median wage is $48.79 / hr.
$44.78 - $50.44
13% of jobs
$50.44 - $56.10
13% of jobs
$59.99 is the 75th percentile. Wages above this are outliers.
$56.10 - $61.76
13% of jobs
$61.76 - $67.42
15% of jobs
$67.42 - $73.08
6% of jobs
$10
$46
$73
How much do temp international qa jobs pay per hour?
What is the difference between Temp International Qa vs Temp International Tester?
| Aspect | Temp International Qa | Temp International Tester |
|---|---|---|
| Primary Role | Quality assurance and process improvement | Product testing and defect identification |
| Required Skills | QA methodologies, documentation, communication | Testing tools, defect tracking, technical knowledge |
| Work Environment | Office, collaborative teams, project-based | Lab, testing facilities, sometimes remote |
| Certifications | QA certifications (e.g., ISTQB), relevant experience | Testing certifications (e.g., ISTQB), technical skills |
Temp International Qa focuses on ensuring quality processes and standards across projects, while Temp International Tester primarily conducts product testing to identify defects. Both roles require knowledge of testing tools and certifications like ISTQB, but Qa emphasizes process improvement and documentation, whereas Tester emphasizes hands-on testing and defect reporting.

Other
Re-posted 6 days ago
Job description
JOB SUMMARY – To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.Â
Responsible for managing the overall Quality Assurance function at AngioDynamics Israel. This involves oversight of the Quality Management System functions including, Management Responsibility, Resource Management, Design & Development, and Measurement, analysis and improvement. The role will require coordinating activities very closely with Corporate QA functional SME's to streamline the reporting and QMS structure. Coordinates activities between QA and other departments to ensure GMP compliance. The person must have the ability to multi-task, prioritize tasks and quickly adjust in a rapidly changing environment.
Essential Duties and Responsibilities
- Responsibility for Quality Assurance Programs that include:
- Report to members of Management and members with Executive Responsibility on the performance of the quality management system and any need for improvement.
- Manage a team of Quality professionals. Ensuring the business unit is sufficiently resourced, development of employees, and perform appraisals. Provide leadership, direction, and coaching to the team.
- Develop and manage site QA budget within overall department budget as necessary.
- Act as Site Management Representative. Coordinate and facilitate external audits with external Regulators and Notified Bodies in conjunction with Corporate Quality.
- Coordinate and prepare annual Management Review in partnership with Corporate QA.
- Provide guidance to the relevant Corporate Quality functions in support of the QMS transition.
- Support the R&D function in their Design & Development projects and coordinate with Design Assurance team to support design verification & validation and implementation of new products and design changes.
- Support Design Assurance team in risk management activities inclusive of product and process risks.
- Support and take the lead in CAPA's as necessary and coordinate with Corporate Quality in system implementation. Support investigations and help implement corrective actions plans.
- Support Complaints Management Team with complaint investigations and help  determine trends. Escalate critical complaints to Complaints Management Team in a timely manner when warranted.
- Support Contract Manufacturer's with supplier changes, non-conformances, root cause analysis, audit activities, etc as necessary. Oversee regular quality reviews and report to Corporate Quality any concerns. Responsible for the release of all finished goods shipped to distribution centers.
- Work with peers and management to develop and deliver monthly management metrics/reviews - analysis of data.
- Ensure compliance with all relevant Regulatory, International standards, and legal requirements. Review and implement any updates to regulations and standards to ensure system compliance.
- Responsible for implementation and maintenance of quality standards to ensure that all new and existing products meet their requirements for safety and effectiveness.
- Interpret and communicate company policies impacting all employees.
- Drives harmonization and best practices across the site.
- Drives quality improvement and customer satisfaction across the site.
- Review current test methods, equipment, procedures, and routine product testing trends to determine the need for change.
- May perform other duties as assigned.
Supervisory Responsibilities
 Yes    Â
Regulatory Responsibilities
- Manages in order to ensure compliance with all relevant regulatory/legal requirements
QUALITY SYSTEMS DUTIES AND RESPONSIBILITIES
Management
Establish and support a work environment of continuous improvement that supports the Quality Policy, Quality System and the appropriate regulations for the area they support. Ensure all employees are trained to do their work and their training is documented
QUALIFICATIONS –The requirements listed below are representative of the knowledge, skill or ability required.
Education and Experience
- Bachelor's Level of Degree in the Engineering or Science related field of study
- 5 years of demonstrated experience in quality assurance with a minimum of 3 years experience within the Medical device industry. In addition a minimum of 3 years supervisory/leadership experience.
- Any preferred education, experience or certifications:Â Advanced graduate degree preferred in a related field.
Â
Skills/Knowledge
- Demonstrated history of execution in a leadership role; adept at personnel selection and development of personnel in key functional roles.
- Successful track record of improvement to organizational Quality functions; ability to correct functional issues with appropriate remedial action.
- Experience in managing through change and proven track record of driving results in changing environments.
- Strong analytical, quantitative and project management skills.
- Working knowledge of Hardware and Software testing methodologies strongly preferred.
- Ability to effectively manage to deadlines while ensuring consistent delivery of top quality results both individually and from direct report team.
- Demonstrated ability to influence decision-making at top levels of an organization by providing guidance and expertise on key matters affecting Quality functions.
- Strong Technical writing skills.
- Demonstrate strong leadership through effective communication, high availability, and operational responsiveness, including flexibility to support the Israel site across non-standard working hours, on site audits in Israel, when required.
- Operate with a hands-on management approach, actively engaging in key quality activities as needed to support the team, resolve issues, and ensure timely execution in a dynamic, fast-paced environment. Exceptional interpersonal skills.
- Strong organizational skills.
- Strong communication skills (written and verbal).
- Ability to effectively communication both internally and externally.
- Ability to read and interpret documents such as safety rules, operating and maintenance, instructions, and procedure manuals. Ability to write routine reports and correspondence.
PHYSICAL/WORK REQUIREMENTS
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:
- Work safely and follow all OSHA regulations and company safety policies and procedures.
- For all on-the-job injuries or accidents, must notify manager/supervisor immediately.
- Exposure to (insert any extreme climate and/or work conditions)Â standard office environment
- Ability to frequently lift and/or move up to 15 Lbs
- Ability to occasionally lift and/or move up to 50 Lbs
- Ability to regularly sit and stand for extended periods of time (insert physical abilities, repetitive movement, vision requirements, etc.)
EMPLOYEE ACKNOWLEDGMENT
By signing the Learning & Development training form, I understand that the company reserves the right to add to or revise an employee’s job duties at any time at its sole discretion. All requirements are subject to possible modification to reasonably accommodate individuals with disabilities. This document does not create a contract of employment between AngioDynamics and any individual, express or implied. All employees are, and remain, employees-at-will.