QMS Administrator
Tampa, FL · On-site
QMS Administrator Location : Tampa, FL Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an ...
Tampa, FL · On-site
QMS Administrator Location : Tampa, FL Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an ...
Tampa, FL · On-site
QMS Administrator Location : Tampa, FL Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an ...
Tampa, FL · On-site
QMS Administrator Location : Tampa, FL Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an ...
Tampa, FL · On-site
QMS Administrator Location : Tampa, FL Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an ...
Tampa, FL · On-site
QMS Administrator Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an exciting opportunity to ...
Tampa, FL · On-site
QMS Administrator Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an exciting opportunity to ...
QMS ADMINISTRATOR Position Summary The Quality Management System (QMS) Administrator is responsible for supporting development, maintenance, and improvement of the organizations QMS with a strong ...
QMS ADMINISTRATOR Position Summary The Quality Management System (QMS) Administrator is responsible for supporting development, maintenance, and improvement of the organizations QMS with a strong ...
Warren, MA · On-site
QMS ADMINISTRATOR Position Summary The Quality Management System (QMS) Administrator is responsible for supporting development, maintenance, and improvement of the organizations QMS with a strong ...
Warren, MA · On-site
QMS ADMINISTRATOR Position Summary The Quality Management System (QMS) Administrator is responsible for supporting development, maintenance, and improvement of the organizations QMS with a strong ...
Newberg, OR · Remote
$86K - $119K/yr
Supports Management Representative with key QMS processes, including Management Review. * Participates as process administrator for weekly customer complaints review process (FACT -Feedback and ...
Newberg, OR · Remote
$86K - $119K/yr
Supports Management Representative with key QMS processes, including Management Review. * Participates as process administrator for weekly customer complaints review process (FACT -Feedback and ...
Newberg, OR · On-site
$86K - $119K/yr
Supports Management Representative with key QMS processes, including Management Review. * Participates as process administrator for weekly customer complaints review process (FACT -Feedback and ...
Newberg, OR · On-site
$86K - $119K/yr
Supports Management Representative with key QMS processes, including Management Review. * Participates as process administrator for weekly customer complaints review process (FACT -Feedback and ...
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Jacksonville, FL · On-site
$62K - $75K/yr
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Jacksonville, FL · On-site
$62K - $75K/yr
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Plan, coordinate, and administer ISO 9001 and BA9000 internal audit activities for ballistic armor ... Own the QMS document control process for supported manufacturing sites, ensuring procedures, forms ...
Cambridge, MA · On-site +1
Administer document control processes within the eQMS, ensuring effective lifecycle management of ... Metrics, Continuous Improvement, and QMS Support * Monitor document control performance, identify ...
Cambridge, MA · On-site +1
Administer document control processes within the eQMS, ensuring effective lifecycle management of ... Metrics, Continuous Improvement, and QMS Support * Monitor document control performance, identify ...
Tallassee, AL · On-site
Their primary purpose is to administer the local QMS/BMS in accordance with the GKN Aerospace Global Standards and local tailoring and to provide core support to the entity/site Leadership team in ...
Tallassee, AL · On-site
Their primary purpose is to administer the local QMS/BMS in accordance with the GKN Aerospace Global Standards and local tailoring and to provide core support to the entity/site Leadership team in ...
Tallassee, AL · On-site
Their primary purpose is to administer the local QMS/BMS in accordance with the GKN Aerospace Global Standards and local tailoring and to provide core support to the entity/site Leadership team in ...
Tallassee, AL · On-site
Their primary purpose is to administer the local QMS/BMS in accordance with the GKN Aerospace Global Standards and local tailoring and to provide core support to the entity/site Leadership team in ...
$75K - $100K/yr
QMS/ISO Compliance Specialist Micro-Matics Inc. is a leader in providing high quality precision ... Administer company corrective and preventive action systems. * Ensure root cause investigations are ...
$75K - $100K/yr
QMS/ISO Compliance Specialist Micro-Matics Inc. is a leader in providing high quality precision ... Administer company corrective and preventive action systems. * Ensure root cause investigations are ...
South Bend, IN · On-site
Administer and maintain QMS processes including CAPA, internal audits and training SOPs. * Lead or support CAPA investigations, ensuring strong root-cause analysis, effectiveness checks, and timely ...
South Bend, IN · On-site
Administer and maintain QMS processes including CAPA, internal audits and training SOPs. * Lead or support CAPA investigations, ensuring strong root-cause analysis, effectiveness checks, and timely ...
Lakeville, MN · On-site
Administer and optimize SharePoint, Intelex, and other QMS systems, databases, and digital resources. * Maintain accurate documentation, coordinate approvals, troubleshoot system issues, and ensure ...
Lakeville, MN · On-site
Administer and optimize SharePoint, Intelex, and other QMS systems, databases, and digital resources. * Maintain accurate documentation, coordinate approvals, troubleshoot system issues, and ensure ...
Lakeville, MN · On-site
Administer and optimize SharePoint, Intelex, and other QMS systems, databases, and digital resources. * Maintain accurate documentation, coordinate approvals, troubleshoot system issues, and ensure ...
Lakeville, MN · On-site
Administer and optimize SharePoint, Intelex, and other QMS systems, databases, and digital resources. * Maintain accurate documentation, coordinate approvals, troubleshoot system issues, and ensure ...
South Bend, IN · On-site
$58K - $70K/yr
Administer and maintain QMS processes including CAPA, internal audits and training SOPs. * Lead or support CAPA investigations, ensuring strong root-cause analysis, effectiveness checks, and timely ...
South Bend, IN · On-site
$58K - $70K/yr
Administer and maintain QMS processes including CAPA, internal audits and training SOPs. * Lead or support CAPA investigations, ensuring strong root-cause analysis, effectiveness checks, and timely ...
South Bend, IN · On-site
Administer and maintain QMS processes including CAPA, internal audits and training SOPs. * Lead or support CAPA investigations, ensuring strong root-cause analysis, effectiveness checks, and timely ...
Quick apply
South Bend, IN · On-site
Administer and maintain QMS processes including CAPA, internal audits and training SOPs. * Lead or support CAPA investigations, ensuring strong root-cause analysis, effectiveness checks, and timely ...
$26K - $34K
3% of jobs
$34K - $42K
5% of jobs
$42K - $50K
5% of jobs
$54.4K is the 25th percentile. Wages below this are outliers.
$50K - $58K
20% of jobs
The median wage is $63K / yr.
$58K - $66K
26% of jobs
$71.3K is the 75th percentile. Wages above this are outliers.
$66K - $74K
23% of jobs
$74K - $82K
7% of jobs
$82K - $90K
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$90K - $98K
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$98K - $106K
2% of jobs
$106K - $114K
1% of jobs
$26K
$67.3K
$114K
A QMS (Quality Management System) Administrator is responsible for maintaining and improving an organization's quality management processes. They ensure compliance with industry standards, manage documentation, conduct audits, and support continuous improvement initiatives. Their role is essential in maintaining certifications such as ISO 9001 by overseeing corrective actions, training employees on quality procedures, and tracking performance metrics.
As a Qms Administrator, your typical day involves managing and updating quality management system documentation, coordinating internal audits, and supporting compliance with industry standards such as ISO 9001. You will also work closely with multiple teams to ensure proper implementation of quality procedures, track corrective actions, and maintain training records for compliance purposes. The role often requires proactive problem-solving and continuous process improvement, making adaptability and collaboration important aspects of daily work. Overall, you help ensure that quality policies are effectively integrated across the organization, contributing to a culture of consistent excellence.
To thrive as a Qms Administrator, you should have a solid understanding of quality management systems, document control, and compliance standards, typically supported by a relevant degree or quality certification. Familiarity with QMS software platforms (such as ISO 9001-compliant systems), audit processes, and regulatory documentation tools is often essential. Strong attention to detail, effective communication, and organizational skills help Qms Administrators excel in managing processes and collaborating with various departments. These qualities are vital for maintaining high-quality standards, ensuring regulatory compliance, and optimizing continuous improvement initiatives within an organization.
The top searched job categories for Qms Administrator jobs are:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 24 days ago
8.3
Based on 42 frontline employees who took The Breakroom Quiz
26th of 86 rated pharmaceutical
QMS Administrator
Location: Tampa, FL
Join our Tampa site as a QMS Administrator and play a key role in strengthening enterprise quality systems that support life-changing therapies. This is an exciting opportunity to contribute to digital transformation, ensuring compliant, efficient document and quality processes across the organization.
This is a fully sitebased role. Working together in person supports close, realtime collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:
Performance-related bonus.
Medical, dental and vision insurance.
401(k) matching plan.
Life insurance, as well as short-term and long-term disability insurance.
Employee assistance programs.
Paid time off (PTO).
Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
Support implementation, administration, and optimization of enterprise Quality Management Systems (QMS) for the Tampa site.
Configure and maintain workflows for document lifecycle, approvals, training, and audit processes.
Lead and support data migration activities, including mapping, validation, and reconciliation of QMS data.
Manage system users, roles, permissions, and ensure access aligns with training compliance requirements.
Collaborate cross-functionally with Quality, IT, Manufacturing, and Regulatory teams to drive system improvements and adoption.
Support system testing, deployment, audits, and inspections while ensuring ongoing FDA and cGMP compliance.
Develop SOPs, work instructions, and quality metrics, while contributing to continuous improvement and mentoring users on best practices.
What we are looking for:
Bachelor's Degree: Information Systems, Computer Science, Engineering, or related field preferred.
5 years of experience supporting enterprise systems, document management platforms, or quality management systems (QMS) in regulated environments.
Strong skills in system configuration, troubleshooting, data analysis, and workflow design.
Proven ability to support system implementations, migrations, or digital transformation initiatives.
Familiarity with QMS platforms such as Documentum, TrackWise, SharePoint, LIMS, Empower, or similar systems.
Ability to interpret and apply FDA, cGMP, or other regulatory requirements to system processes.
Effective communication and organizational skills with the ability to collaborate across functions.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
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Biotechnology research and development and pharmaceutical and medicine manufacturing
10,000+ Employees
Bern, KS, US