SUMMARY/OBJECTIVE This position supports activities of the Quality Assurance Department regarding ... The QA Associate II/III independently conducts quality assurance audits of production records ...
SUMMARY/OBJECTIVE This position supports activities of the Quality Assurance Department regarding ... The QA Associate II/III independently conducts quality assurance audits of production records ...
Quality Technician
Lincoln, RI · On-site
$28 - $30.25/hr
We're looking for a high‑energy, detail‑driven Quality Technician / Quality Support ... Train production associates on: * Inspection equipment. * Testing procedures. * Data entry and ...
Quick apply
Quality Technician
Lincoln, RI · On-site
$28 - $30.25/hr
We're looking for a high‑energy, detail‑driven Quality Technician / Quality Support ... Train production associates on: * Inspection equipment. * Testing procedures. * Data entry and ...
Job Summary The Associate Chief Nursing Officer (ACNO), Ambulatory Services, serves as the senior ... Collaborates with executive leadership to establish priorities that support quality, growth ...
Job Summary The Associate Chief Nursing Officer (ACNO), Ambulatory Services, serves as the senior ... Collaborates with executive leadership to establish priorities that support quality, growth ...
Quality Technician
Bristol, RI · On-site
$18.75 - $25.25/hr
Experience supporting or managing a calibration program * Detail-oriented and organized ... associate degree or technical certificate a plus Preferred Skills * Experience in start-up ...
Quality Technician
Bristol, RI · On-site
$18.75 - $25.25/hr
Experience supporting or managing a calibration program * Detail-oriented and organized ... associate degree or technical certificate a plus Preferred Skills * Experience in start-up ...
Quality Technician
$18.75 - $25.25/hr
Experience supporting or managing a calibration program * Detail-oriented and organized ... associate degree or technical certificate a plus Preferred Skills * Experience in start-up ...
Quality Technician
$18.75 - $25.25/hr
Experience supporting or managing a calibration program * Detail-oriented and organized ... associate degree or technical certificate a plus Preferred Skills * Experience in start-up ...
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
New
Quick apply
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
New
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
Provides analyzed data reports as necessary to support the plant.* Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
Provides analyzed data reports as necessary to support the plant.* Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Job Summary The Associate Chief Nursing Officer (ACNO), Ambulatory Services, serves as the senior ... Collaborates with executive leadership to establish priorities that support quality, growth ...
Job Summary The Associate Chief Nursing Officer (ACNO), Ambulatory Services, serves as the senior ... Collaborates with executive leadership to establish priorities that support quality, growth ...
Quality Manager
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
Quick apply
Quality Manager
Lincoln, RI · On-site
$97K - $145K/yr
Provides analyzed data reports as necessary to support the plant. * Recruits quality assurance associates, as appropriate, and provides the necessary training so that their work is in accordance with ...
In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during ...
In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during ...
Manufacturing and Quality Technician
Warwick, RI · On-site
$48K - $60K/yr
This role is responsible for ensuring product quality and supporting the assembly and testing of ... High school diploma or equivalent; technical certification or associate degree preferred.
Quick apply
Manufacturing and Quality Technician
Warwick, RI · On-site
$48K - $60K/yr
This role is responsible for ensuring product quality and supporting the assembly and testing of ... High school diploma or equivalent; technical certification or associate degree preferred.
Manufacturing and Quality Technician
Warwick, RI · On-site
$48K - $60K/yr
This role is responsible for ensuring product quality and supporting the assembly and testing of ... High school diploma or equivalent; technical certification or associate degree preferred.
Quick apply
Manufacturing and Quality Technician
Warwick, RI · On-site
$48K - $60K/yr
This role is responsible for ensuring product quality and supporting the assembly and testing of ... High school diploma or equivalent; technical certification or associate degree preferred.
DVM
$107K - $204K/yr
If you are a current associate, you will need to apply through our internal career site. Please log ... support quality of life School loan assistance through our Student Debt Relief Program Equity ...
DVM
$107K - $204K/yr
If you are a current associate, you will need to apply through our internal career site. Please log ... support quality of life School loan assistance through our Student Debt Relief Program Equity ...
This role is responsible for ensuring product quality and supporting the assembly and testing of ... High school diploma or equivalent; technical certification or associate degree preferred.
This role is responsible for ensuring product quality and supporting the assembly and testing of ... High school diploma or equivalent; technical certification or associate degree preferred.
Specialist QC
West Greenwich, RI · On-site
In this vital role you will support analytical investigations ownership within the QC Technical ... Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ...
Specialist QC
West Greenwich, RI · On-site
In this vital role you will support analytical investigations ownership within the QC Technical ... Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ...
Living Donor Outreach Specialist
Providence, RI · On-site
$50K - $83K/yr
Support quality improvement and program development initiatives. * Maintain accurate reporting and donor tracking systems. QUALIFICATIONS * Associate's degree required, Bachelor's degree in health ...
Living Donor Outreach Specialist
Providence, RI · On-site
$50K - $83K/yr
Support quality improvement and program development initiatives. * Maintain accurate reporting and donor tracking systems. QUALIFICATIONS * Associate's degree required, Bachelor's degree in health ...
Support Quality Associate information
What cities in Rhode Island are hiring for Support Quality Associate jobs?
Cities in Rhode Island with the most Support Quality Associate job openings:
Quality Assurance Associate I (Cumberland, RI)
Cumberland, RI • On-site
Cedent
• IT Services • 11 - 50 employees11 - 50 employees
Full-time
Re-posted 24 days ago
Job description
SUMMARY/OBJECTIVE
This position supports activities of the Quality Assurance Department regarding pharmaceutical manufacturing, testing and packaging to ensure compliance with all relevant pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations, investigations and CAPA. Adheres to Client compliance initiatives, including
following all quality and division/company policy requirements. Helps to ensure that all Client products meet quality requirements by supporting all assigned quality aspects of product approval. The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards are maintained and product integrity is preserved.
RESPONSIBILITIES
1. Provide support to GMP investigations, validation documentation review and approval, identify gaps within existing Quality Systems and propose solutions for functional management;
2. Participates/leads internal/external audits, prepare and issue audit reports. Recommend remediation actions and follow up on implementation of the plan.
3. Supports resolution of technical and compliance issues/gap analysis.
4. Aides implementation of Quality Systems/System Improvements.
5. Supports and assists with Quality systems-related training, including compliance with cGMP and SOPs.
6. Interface with key quality, manufacturing, customers and coordinate documentation impacting quality areas.
7. Review/approval of all cGMP documents generated across site to include (but not limited to): SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control, deviation & document revisions, etc.
8. Participates in activities associated with primary batch record review, non-conformances investigation and CAPA.
9. Work in coordination with regulatory affairs group in support of ANDA submissions.
10. Provides QA review/approval of all cGMP documents associated with manufacture of product.
11. Communicates with contractors and internal manufacturing/technical groups regarding compliance and quality issues (i.e., batch documentation, investigations, timelines and data related issues).
12. Authors or revises SOPs as necessary.
13. Actively engaged in the training of staff with lesser experience or knowledge of quality assurance processes. Educate and instruct QA and plant personnel in quality best practices for sampling, labeling,
good documentation practices, equipment sanitation. Confirm these procedures are being adhered to, taking corrective actions when non-conformances are observed.
14. Routinely provide input to quality and operations management for better operational procedures to improve overall efficiency and regulatory compliance.
15. Assist in development of special department projects and work in conjunction with quality management.
16. Other duties as assigned.
COMPETENCIES
1. Project Management
2. Technical Capacity.
3. Discretion.
4. Problem Solving/Analysis.
5. Decision Making.
6. Communication Proficiency.
7. Collaboration Skills.
8. Learning Agility
9. Managing Changing Priorities
POSITION TYPE/EXPECTED HOURS OF WORK
This is a full-time position requiring 40 or more hours of work per week.
This position supports activities of the Quality Assurance Department regarding pharmaceutical manufacturing, testing and packaging to ensure compliance with all relevant pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations, investigations and CAPA. Adheres to Client compliance initiatives, including
following all quality and division/company policy requirements. Helps to ensure that all Client products meet quality requirements by supporting all assigned quality aspects of product approval. The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards are maintained and product integrity is preserved.
RESPONSIBILITIES
1. Provide support to GMP investigations, validation documentation review and approval, identify gaps within existing Quality Systems and propose solutions for functional management;
2. Participates/leads internal/external audits, prepare and issue audit reports. Recommend remediation actions and follow up on implementation of the plan.
3. Supports resolution of technical and compliance issues/gap analysis.
4. Aides implementation of Quality Systems/System Improvements.
5. Supports and assists with Quality systems-related training, including compliance with cGMP and SOPs.
6. Interface with key quality, manufacturing, customers and coordinate documentation impacting quality areas.
7. Review/approval of all cGMP documents generated across site to include (but not limited to): SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control, deviation & document revisions, etc.
8. Participates in activities associated with primary batch record review, non-conformances investigation and CAPA.
9. Work in coordination with regulatory affairs group in support of ANDA submissions.
10. Provides QA review/approval of all cGMP documents associated with manufacture of product.
11. Communicates with contractors and internal manufacturing/technical groups regarding compliance and quality issues (i.e., batch documentation, investigations, timelines and data related issues).
12. Authors or revises SOPs as necessary.
13. Actively engaged in the training of staff with lesser experience or knowledge of quality assurance processes. Educate and instruct QA and plant personnel in quality best practices for sampling, labeling,
good documentation practices, equipment sanitation. Confirm these procedures are being adhered to, taking corrective actions when non-conformances are observed.
14. Routinely provide input to quality and operations management for better operational procedures to improve overall efficiency and regulatory compliance.
15. Assist in development of special department projects and work in conjunction with quality management.
16. Other duties as assigned.
COMPETENCIES
1. Project Management
2. Technical Capacity.
3. Discretion.
4. Problem Solving/Analysis.
5. Decision Making.
6. Communication Proficiency.
7. Collaboration Skills.
8. Learning Agility
9. Managing Changing Priorities
POSITION TYPE/EXPECTED HOURS OF WORK
This is a full-time position requiring 40 or more hours of work per week.
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008