Specialist QA
Juncos, PR · On-site
COMPETENCIES/SKILLS - Project management skills. - Strong organizational skills, including ability ... QA, QAL, validation and process development. - Demonstrate ability to interact with regulatory ...
Specialist QA
Juncos, PR · On-site
COMPETENCIES/SKILLS - Project management skills. - Strong organizational skills, including ability ... QA, QAL, validation and process development. - Demonstrate ability to interact with regulatory ...
PR · On-site
The QA Supervisor is responsible for overseeing and coordinating quality assurance activities ... Prepare quality reports and present findings to management. Qualifications:Education: * Bachelor ...
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PR · On-site
The QA Supervisor is responsible for overseeing and coordinating quality assurance activities ... Prepare quality reports and present findings to management. Qualifications:Education: * Bachelor ...
... for QA manager on local CCRB. - Review Risk Assessments. - Support Automation activities. Requirements: -Doctorate OR -Masters + 2 years of directly related experience OR -Bachelors + 4 years of ...
... for QA manager on local CCRB. - Review Risk Assessments. - Support Automation activities. Requirements: -Doctorate OR -Masters + 2 years of directly related experience OR -Bachelors + 4 years of ...
How about this one? We're seeking an Specialist QA to work with one of our top global ... Fully Bilingual in English and Spanish. • Alerts senior management of quality, compliance, supply ...
How about this one? We're seeking an Specialist QA to work with one of our top global ... Fully Bilingual in English and Spanish. • Alerts senior management of quality, compliance, supply ...
How about this one? We're seeking an Specialist QA to work with one of our top global ... Fully Bilingual in English and Spanish. • Alerts senior management of quality, compliance, supply ...
Quick apply
How about this one? We're seeking an Specialist QA to work with one of our top global ... Fully Bilingual in English and Spanish. • Alerts senior management of quality, compliance, supply ...
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Specialist QA (5:00 pm - 5:30 am) SUMMARY Perform one or more of the following duties and ...
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Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Specialist QA (5:00 pm - 5:30 am) SUMMARY Perform one or more of the following duties and ...
Maintain accurate QA documentation, including inspection records, non-conformance reports, and ... Associate's or Bachelor's degree in Quality Management, Engineering, or related field preferred ...
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Maintain accurate QA documentation, including inspection records, non-conformance reports, and ... Associate's or Bachelor's degree in Quality Management, Engineering, or related field preferred ...
QA Coordinator
Hatillo, PR · On-site
Maintain accurate QA documentation, including inspection records, non-conformance reports, and ... Associate's or Bachelor's degree in Quality Management, Engineering, or related field preferred ...
QA Coordinator
Hatillo, PR · On-site
Maintain accurate QA documentation, including inspection records, non-conformance reports, and ... Associate's or Bachelor's degree in Quality Management, Engineering, or related field preferred ...
Maintain accurate QA documentation, including inspection records, non-conformance reports, and ... Associate's or Bachelor's degree in Quality Management, Engineering, or related field preferred ...
Maintain accurate QA documentation, including inspection records, non-conformance reports, and ... Associate's or Bachelor's degree in Quality Management, Engineering, or related field preferred ...
PR · On-site
Ensuring product quality and compliance with IMS (Integrated Management System,), ISO 9001 and ... and maintain QA QC procedures and protocols. · SCAR (Supplier Corrective Action Request)
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PR · On-site
Ensuring product quality and compliance with IMS (Integrated Management System,), ISO 9001 and ... and maintain QA QC procedures and protocols. · SCAR (Supplier Corrective Action Request)
Specialist QA
Juncos, PR · On-site
Alerts senior management of quality, compliance, supply, and safety risks. * Supports internal/external audits and inspections as needed. Shift : Administrative Location : Juncos, PR Education:
Specialist QA
Juncos, PR · On-site
Alerts senior management of quality, compliance, supply, and safety risks. * Supports internal/external audits and inspections as needed. Shift : Administrative Location : Juncos, PR Education:
Alerts senior management of quality, compliance, supply, and safety risks. * Supports internal/external audits and inspections as needed. Shift : Administrative Location : Juncos, PR Education:
Alerts senior management of quality, compliance, supply, and safety risks. * Supports internal/external audits and inspections as needed. Shift : Administrative Location : Juncos, PR Education:
PR · On-site
Manage defect tracking, prioritization, and resolution with engineering teams * Enforce QA validation as part of the release process Cross-Functional Collaboration * Work closely with Fintech ...
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PR · On-site
Manage defect tracking, prioritization, and resolution with engineering teams * Enforce QA validation as part of the release process Cross-Functional Collaboration * Work closely with Fintech ...
Specialist QA 35382
Juncos, PR · On-site
Administrative Shift Under minimal supervision, support Quality Assurance program by performing a variety of key responsibilities in manufacturing, process validation, regulatory compliance, and ...
Specialist QA 35382
Juncos, PR · On-site
Administrative Shift Under minimal supervision, support Quality Assurance program by performing a variety of key responsibilities in manufacturing, process validation, regulatory compliance, and ...
$14/hr
We are currently seeking a QA Laboratory Technician to join one of our top clients in the medical device and pharmaceutical industry, located in San Lorenzo, PR . * Compensation: $14.00 hour, shift ...
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$14/hr
We are currently seeking a QA Laboratory Technician to join one of our top clients in the medical device and pharmaceutical industry, located in San Lorenzo, PR . * Compensation: $14.00 hour, shift ...
We are currently seeking a QA Laboratory Technician to join one of our top clients in the medical device and pharmaceutical industry, located in San Lorenzo, PR . * Compensation: $14.00 hour, shift ...
We are currently seeking a QA Laboratory Technician to join one of our top clients in the medical device and pharmaceutical industry, located in San Lorenzo, PR . * Compensation: $14.00 hour, shift ...
Specialist QA - 35382
Juncos, PR · On-site
Position Summary We are seeking a highly motivated Specialist QA to support Environmental ... Present EM/CU data in quality forums and management review meetings , including recommendations ...
Specialist QA - 35382
Juncos, PR · On-site
Position Summary We are seeking a highly motivated Specialist QA to support Environmental ... Present EM/CU data in quality forums and management review meetings , including recommendations ...
Activelyparticipatein deviation and RCA meetings, managing multiple concurrent deviations and ... Quality Assurance experience OR High school diploma / GED and 10 years of Quality ...
Activelyparticipatein deviation and RCA meetings, managing multiple concurrent deviations and ... Quality Assurance experience OR High school diploma / GED and 10 years of Quality ...
... the QA Manager and/or other interested parties. Performs all duties associated with compliance ... Experience with Quality Risk Management, Problem Solving and Statistical Analysis, and Project ...
... the QA Manager and/or other interested parties. Performs all duties associated with compliance ... Experience with Quality Risk Management, Problem Solving and Statistical Analysis, and Project ...
PR · On-site
... the QA signature. * Maintain and control the Validation Change Control Program for the validated/qualified systems and the Validation Management System (VMS). * Review and approval of Validation ...
Qa Manager information
How does a QA Manager typically collaborate with development and product teams to ensure software quality?
A QA Manager works closely with both development and product teams to align testing strategies with project requirements and timelines. This collaboration often involves participating in sprint planning meetings, defining acceptance criteria, and facilitating communication to address quality concerns early in the development cycle. By fostering a culture of transparency and continuous feedback, QA Managers help ensure that issues are identified and resolved efficiently, resulting in a higher-quality end product. Effective collaboration also enables QA Managers to advocate for testing best practices and drive improvements across the software development lifecycle.
What is a QA Manager?
A QA Manager, or Quality Assurance Manager, is responsible for overseeing the quality assurance processes within an organization. They develop and implement testing strategies, manage QA teams, and ensure that products or services meet established quality standards before reaching customers. QA Managers collaborate closely with development, operations, and product teams to identify defects, improve processes, and maintain compliance with industry regulations. Their work is crucial for minimizing errors, enhancing customer satisfaction, and supporting continuous improvement.
What Is a QA Manager?
As a QA manager, you oversee the quality assurance (QA) team and make sure that no defective products make it to customers. Your job duties include hiring and training QA inspectors, managing quality control procedures and the operations of the QA department, and ensuring that products meet specifications and are safe for consumer use. As a QA manager, your work is primarily in production and manufacturing, where you ensure the quality of goods like cars, clothes, electronics, and food items.
What are the key skills and qualifications needed to thrive as a QA Manager, and why are they important?
To thrive as a QA Manager, you need expertise in quality assurance methodologies, test planning, and process improvement, often supported by a degree in computer science or engineering and relevant experience. Familiarity with test automation tools (like Selenium or JIRA), software development life cycle (SDLC) systems, and certifications such as ISTQB or Six Sigma are typically required. Strong leadership, communication, and problem-solving skills help you manage teams effectively and advocate for quality across departments. These competencies ensure the delivery of high-quality products, foster team productivity, and drive continuous improvement in testing processes.
Is QA a difficult job?
Quality Assurance (QA) managers oversee testing processes to ensure product quality, which can involve complex problem-solving, attention to detail, and understanding of testing tools and methodologies. The difficulty of the role depends on the complexity of projects, team coordination, and technical requirements, but it generally requires strong analytical skills and experience in software testing or quality standards.
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Job description
SUMMARY
Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision.
FUNCTIONS
- Review and approve product MPs.
- Approve process validation protocols and reports for manufacturing processes.
- Request Quality on incident triage team.
- Approve Environmental Characterization reports.
- Release of sanitary utility systems.
- Approve planned incidents.
- Represent QA on NPI team.
- Lead investigations.
- Lead site audits.
- Own site quality program procedures.
- Designee for QA manager on local CCRB.
- Review Risk Assessments.
- Support Automation activities.
- Support facilities and environmental programs.
- Review and approve Work Orders.
- Review and approve EMS/BMS alarms.
- Approve NC investigations and CAPA records.
- Approve change controls.
- Provide lot disposition and authorize lots for shipment.
EDUCATION
-Doctorate OR
-Masters + 2 years of directly related experience OR
-Bachelors + 4 years of directly related experience OR
-Associates + 8 years of directly related experience OR
-High school/GED + 10 years of directly related experience.
COMPETENCIES/SKILLS
- Project management skills.
- Strong organizational skills, including ability to follow assignments through to completion.
- Initiate and lead cross functional teams.
- Enhanced skills in leading, influencing and negotiating.
- Strong knowledge in area of expertise.
- Collaborate and coordinate with higher level outside resources.
- Strong knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation and process development.
- Demonstrate ability to interact with regulatory agencies.
- Strong word processing, presentation, database and spreadsheet application skills.
- Strong communication (both written and oral), facilitation and presentation skills.
- Strong skill in working independently and to effectively interact with various levels.
- Advanced data trending and evaluation.
- Ability to evaluate compliance issues.
- Demonstrate the Client Values/Leadership Practices.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*
Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision.
FUNCTIONS
- Review and approve product MPs.
- Approve process validation protocols and reports for manufacturing processes.
- Request Quality on incident triage team.
- Approve Environmental Characterization reports.
- Release of sanitary utility systems.
- Approve planned incidents.
- Represent QA on NPI team.
- Lead investigations.
- Lead site audits.
- Own site quality program procedures.
- Designee for QA manager on local CCRB.
- Review Risk Assessments.
- Support Automation activities.
- Support facilities and environmental programs.
- Review and approve Work Orders.
- Review and approve EMS/BMS alarms.
- Approve NC investigations and CAPA records.
- Approve change controls.
- Provide lot disposition and authorize lots for shipment.
EDUCATION
-Doctorate OR
-Masters + 2 years of directly related experience OR
-Bachelors + 4 years of directly related experience OR
-Associates + 8 years of directly related experience OR
-High school/GED + 10 years of directly related experience.
COMPETENCIES/SKILLS
- Project management skills.
- Strong organizational skills, including ability to follow assignments through to completion.
- Initiate and lead cross functional teams.
- Enhanced skills in leading, influencing and negotiating.
- Strong knowledge in area of expertise.
- Collaborate and coordinate with higher level outside resources.
- Strong knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation and process development.
- Demonstrate ability to interact with regulatory agencies.
- Strong word processing, presentation, database and spreadsheet application skills.
- Strong communication (both written and oral), facilitation and presentation skills.
- Strong skill in working independently and to effectively interact with various levels.
- Advanced data trending and evaluation.
- Ability to evaluate compliance issues.
- Demonstrate the Client Values/Leadership Practices.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*
About Weil Group
Sourced by ZipRecruiter
Company size
1 - 10 Employees
Headquarters location
Richmond, VA, US
Year founded
2011