Specialist QA
Juncos, PR · On-site
SUMMARY Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision. What attributes (i.e. - preferred qualifications ...
Quick apply
Specialist QA
Juncos, PR · On-site
SUMMARY Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision. What attributes (i.e. - preferred qualifications ...
PR · On-site
Medical
Dental
Vision
Life
Retirement
The Quality Associate supports the Global Biologics Quality Function within Operations. Expectations that the Quality Associate III will maintain high-quality levels on all aspects of their job ...
Quick apply
PR · On-site
Medical
Dental
Vision
Life
Retirement
The Quality Associate supports the Global Biologics Quality Function within Operations. Expectations that the Quality Associate III will maintain high-quality levels on all aspects of their job ...
PR · On-site
Medical
Dental
Vision
Life
Retirement
PTO
As the Quality Assurance Specialist, you will play a vital role in the PharmaLogic quality program to assure compliance with cGMP and other standards for the manufacture of PET drugs for ...
Quick apply
PR · On-site
Medical
Dental
Vision
Life
Retirement
PTO
As the Quality Assurance Specialist, you will play a vital role in the PharmaLogic quality program to assure compliance with cGMP and other standards for the manufacture of PET drugs for ...
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Sales Coordinator
San Juan, PR · On-site
$35K - $38K/yr
Sales Coordinator Join Our Team At Alma San Juan, Autograph Collection, we create memorable guest ... Each hotel is thoughtfully chosen for its quality, originality, bold character, and ability to ...
Sales Coordinator
San Juan, PR · On-site
$35K - $38K/yr
Sales Coordinator Join Our Team At Alma San Juan, Autograph Collection, we create memorable guest ... Each hotel is thoughtfully chosen for its quality, originality, bold character, and ability to ...
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Sales Coordinator
San Juan, PR · On-site
$35K - $38K/yr
Sales Coordinator Join Our Team At Alma San Juan, Autograph Collection, we create memorable guest ... Each hotel is thoughtfully chosen for its quality, originality, bold character, and ability to ...
Sales Coordinator
San Juan, PR · On-site
$35K - $38K/yr
Sales Coordinator Join Our Team At Alma San Juan, Autograph Collection, we create memorable guest ... Each hotel is thoughtfully chosen for its quality, originality, bold character, and ability to ...
Sr. Supplier Quality Engineer
Juncos, PR · On-site
Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for ...
Sr. Supplier Quality Engineer
Juncos, PR · On-site
Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for ...
$38/hr
Medical
Dental
Vision
Life
Retirement
Opportunity to contribute to industry-leading quality assurance and compliance programs * Work with a highly respected organization in the biopharmaceutical sector * Gain valuable experience in ...
Quick apply
$38/hr
Medical
Dental
Vision
Life
Retirement
Opportunity to contribute to industry-leading quality assurance and compliance programs * Work with a highly respected organization in the biopharmaceutical sector * Gain valuable experience in ...
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
$12.75 - $16.50/hr
... quality, expedites, complaints , and returns. Answering emails and customer inquiries in a ... Coordination: Coordinate with external partners and other departments, such as marketing, finance ...
$12.75 - $16.50/hr
... quality, expedites, complaints , and returns. Answering emails and customer inquiries in a ... Coordination: Coordinate with external partners and other departments, such as marketing, finance ...
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
PR · On-site
Support QA oversight of Site Utilities Systems and Environmental Monitoring results. Coordinate with impacted areas including the laboratory, utilities, and manufacturing operations. Ensure ...
Quick apply
PR · On-site
Support QA oversight of Site Utilities Systems and Environmental Monitoring results. Coordinate with impacted areas including the laboratory, utilities, and manufacturing operations. Ensure ...
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
Quick apply
Drafting Support and Coordinator Description: Provides drafting support and coordination for ... Support documentation control activities to maintain service quality and continuity. Qualifications:
PR · On-site
Medical
Dental
Vision
Retirement
PTO
The Specialist, Quality Assurance is responsible for QA batch record review and disposition assuring that bulk and finished products batch record documentation complies with Abbvie policies ...
Specialist Quality Assurance
Juncos, PR · On-site
For QA Services in the Downstream area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's Degree with five (5) years of experience within the pharmaceutical or regulated industry. * Bilingual ...
Specialist Quality Assurance
Juncos, PR · On-site
For QA Services in the Downstream area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's Degree with five (5) years of experience within the pharmaceutical or regulated industry. * Bilingual ...
Specialist QA
Juncos, PR · On-site
SUMMARY Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision. What attributes (i.e. - preferred qualifications ...
Specialist QA
Juncos, PR · On-site
SUMMARY Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision. What attributes (i.e. - preferred qualifications ...
Quality Coordinator information
What is a quality coordinator?
Quality coordinators ensure that employees follow quality assurance standards and procedures established by the company. As a quality coordinator, you analyze data, review policies, and suggest process improvements. You create reports and train employees on expectations of quality goals. Depending on the industry, your job may involve product testing, customer service audits, or reviewing operations data. Qualifications to become a quality coordinator include several years of production experience in the industry in which you wish to work.
What does a quality coordinator do?
A Quality Coordinator is responsible for ensuring that an organization’s products or services meet established standards of quality, including reliability, usability, and performance. They develop and implement quality assurance processes, conduct audits, and monitor compliance with industry regulations. Quality Coordinators also collaborate with other departments to address quality issues, provide training on quality standards, and help drive continuous improvement initiatives. Their goal is to maintain high standards and minimize defects or errors in products and services.
What are the key skills and qualifications needed to thrive as a quality coordinator, and why are they important?
To thrive as a Quality Coordinator, you need a solid understanding of quality management principles, process improvement methodologies, and relevant industry standards, often supported by a degree in quality assurance or a related field. Familiarity with quality management systems (QMS), ISO standards, and data analysis tools like Six Sigma or Lean certifications is typically required. Strong attention to detail, effective communication, and problem-solving abilities are vital soft skills that set top-performing Quality Coordinators apart. These competencies are crucial for ensuring compliance, driving continuous improvement, and maintaining high standards within an organization.
What are some common challenges faced by quality coordinators, and how can they be effectively managed?
Quality Coordinators often encounter challenges such as ensuring compliance with evolving industry standards, managing documentation accuracy, and fostering consistent communication across departments. To effectively manage these issues, it's important to stay updated on regulatory changes, implement robust document control systems, and build strong relationships with both production and management teams. Proactive problem-solving and ongoing training are also key to maintaining a high standard of quality across all processes.
What is the difference between Quality Coordinator vs Quality Inspector?
| Aspect | Quality Coordinator | Quality Inspector |
|---|---|---|
| Certifications | ISO 9001, Six Sigma, quality management certifications | ISO 9001, industry-specific inspection certifications |
| Work Environment | Office-based, coordinating quality processes across departments | Manufacturing or production floor, inspecting products |
| Primary Responsibilities | Developing quality procedures, coordinating audits, ensuring compliance | Inspecting products, identifying defects, recording inspection results |
While both roles focus on quality, the Quality Coordinator manages quality systems and processes, whereas the Quality Inspector performs hands-on product inspections. The Coordinator ensures overall compliance and process improvement, while the Inspector verifies product quality at specific stages.
What skills do you need to be a quality coordinator?
A quality coordinator needs strong attention to detail, excellent communication skills, and knowledge of quality management systems and standards. They should be proficient in data analysis, problem-solving, and often use tools like spreadsheets or quality software. Certifications such as Six Sigma or ISO auditor training can also enhance their qualifications.
More about Quality Coordinator jobs
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The most popular types of Quality jobs in Puerto Rico are:
What are popular job titles related to Quality Coordinator jobs in Puerto Rico?
For Quality Coordinator jobs in Puerto Rico, the most frequently searched job titles are:
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The top searched job categories for Quality Coordinator jobs in Puerto Rico are:
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Cities in Puerto Rico with the most Quality Coordinator job openings:
Full-time
This job post has expired 2 days ago. Applications are no longer accepted.
Job description
SUMMARY
Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision.
What attributes (i.e. - preferred qualifications) would make this candidate stand out?
The candidate should poses a BS in Science, Engineering, Physics, Biology, Chemistry or related fields. It should have experienced working in biopharmaveutical industry, quality organization supporting deviations, validation reports, qualifications, investigations, at least 5 years of experienced in a highly regulated environment .
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.
What attributes (i.e. - preferred qualifications) would make this candidate stand out?
The candidate should poses a BS in Science, Engineering, Physics, Biology, Chemistry or related fields. It should have experienced working in biopharmaveutical industry, quality organization supporting deviations, validation reports, qualifications, investigations, at least 5 years of experienced in a highly regulated environment .
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