TRIMEDX
Quality & Regulatory Compliance Analyst - CONTRACTOR
TRIMEDX, Indianapolis, Indiana, us, 46262
Quality & Regulatory Compliance Analyst - CONTRACTOR
Join to apply for the Quality & Regulatory Compliance Analyst - CONTRACTOR role at TRIMEDX.
Company Culture
Everyone is focused on serving the customer and we do that by collaborating and supporting each other
Associates look forward to coming to work each day
Every associate matters and makes a difference
The Quality & Regulatory Compliance Analyst - CONTRACTOR is an integral role in producing standard compliance data for accreditation and regulatory surveys, internal QRC and Supplier Quality audits and data audits, CAPA effectiveness, as well as normalized and standardized MMD categorization. This position will work directly with the Quality and Regulatory Compliance team, as well as field operations to drive reporting, analysis and data integrity regarding compliance to Accreditation Standards, as well as Federal, State and Local Regulations. The Quality & Regulatory Compliance Analyst leverages large and varied datasets to support compliance initiatives and programs across the organization.
Contractor:
This role is for a Contractor, for a fixed duration of time for 8-12 months, and will be contracted through our third‑party vendor partner agency.
Pay Rate: $35 per hour
Location:
Eastern or Central Time Zone; Indianapolis preferred. Our Central Office is located on the northwest side of Indianapolis.
Relocation is not available for this contract
Immigration sponsorship not available for this contract
Responsibilities Compliance Analytics and Reporting (50%)
Conduct targeted analysis of repair and preventive maintenance data related to QRC internal audits and data audits criteria to ensure compliance to federal, state and local regulations and accreditation standards
Compile data and perform analysis for equipment make/models/description and modalities, as well as equipment risk to ensure standardized MMD creation, maintenance and improvement
Support Quality and Regulatory Specialists with reporting criteria and analysis of effectiveness verification post audit and CAPA completion
Identification, monitoring and assistance with risk/opportunity assessment across the organization
Provide oversight, monitoring and analysis with regulatory compliance requirements
Assist with MMD matching of new and existing customer inventory in accordance with TRIMEDX MMD standardization processes and best practices
Conduct analysis and comparison of alerts and recalls in determining impact to TRIMEDX organization and timely closure of loop
Monitor, measure and produce QRC reporting necessary for Quality Management Review on a monthly/quarterly basis
Support Quality and Regulatory Specialists with reporting criteria during site inspections and surveys
QRC Tools, Processes and Program (30%)
Lead QMS internal audit activities (per ISO 13485, 27001 and/or applicable regulatory standards)
Create, manage and monitor PM Transition Plan and Tools for new site implementations and existing sites with PM compliance gaps
Based on data analysis results and organizational feedback, partner with cross‑functional areas when the development of new processes, products, services, or relationships is required
Develop best practices and business rules to ensure uniformity in work, deliverables and outcomes
Assist with creation, analysis and maintaining standardized reporting of Pilgrim CAPA progress and effectiveness verification
Creation, maintenance and improvement of data audit and remote internal audit tool for QRC team and external field‑facing documentation
Participate in AEM (Alternative Equipment Maintenance) and PM Variance Committee by producing pertinent data pull and analysis related to PM Frequency Change and AEM Program requests and speak to outcome of analysis to committee members to drive decision‑making processes related to equipment risk and PM frequencies
Monitor, measure and communicate compliance gaps and risks in a timely manner to ensure mitigation of risks to patient safety and compliance
Demonstrate competency as a QRC subject matter expert for RSQ and QMS software program analysis
Assist with prompt response and actions related to QRC ServiceNow requests (PM Frequency Changes, PM Not Needed Requests, AEM Program Review, Bulk QRC requests)
Communication and Interactions (20%)
Collaborate with cross‑functional business leaders to capture and document QRC reporting and analytics needs
Create and deliver QRC presentation data support and communications to peers, functional area leaders, and executives
Collaborate with QRC team and Field Operations to ensure timely deliverables requested on behalf of surveyor during regulatory and accreditation survey process
Participate in PM Variance and AEM Committees to share QRC analysis with group to drive outcomes based upon compliance
All other duties as assigned.
Skills And Experience
Minimum of 3 years of experience in clinical engineering, quality, compliance, with demonstrated competency in data analysis, reporting, and application of problem solving
Experience with complex reporting and analysis to ensure QRC data integrity and compliance
Strong demonstrated proficiency with Microsoft Office applications; advanced skills with Advanced Excel and Access required (Sequel, Qlik, Tableau experience a plus)
Basic knowledge and application of ISO 13485, 9001 and/or 27001 standards and applicable regulations
Knowledge of healthcare industry, regulatory compliance, clinical engineering, medical technology, and/or healthcare support services preferred
Knowledge of ISO 9001, 13485 and/or 27001 preferred
Strong analytical and interpretation skills to understand complex regulations and data analysis related to compliance
Strong written and verbal communication skills supporting interactions with personnel at all levels within the organization
Creative thinker with ability to meet stringent and changing deadlines with accuracy
Change management and customer focused
Education And Qualifications
Associate's degree in Quality and/or Regulatory Compliance, Clinical Engineering, Applied Science or Business equivalent or equivalent experience required.
Bachelor’s degree preferred.
At TRIMEDX, we are committed to cultivating a workplace culture where every associate feels valued, supported, and empowered to thrive. This culture reflects our belief that our people are our foundation, their well‑being is essential, and shared success is built through meaningful work, recognition, and opportunities for growth.
We embrace people’s differences which include age, race, color, ethnicity, gender, gender identity, sexual orientation, national origin, education, genetics, veteran status, disability, religion, beliefs, opinions and life experiences.
Visit our website to view our Workplace Culture Commitment, along with our social channels to see what our team is up to: Facebook, LinkedIn, Twitter.
TRIMEDX is an Equal Opportunity Employer. Drug-Free Workplace.
Because we are committed to providing a safe and productive work environment, TRIMEDX is a drug‑free workplace. Accordingly, Associates are prohibited from engaging in the unlawful manufacture, sale, distribution, dispensation, possession, or use of any controlled substance or marijuana, or otherwise being under the influence thereof, on all TRIMEDX and Customer property or during working/on‑call hours.
Job Details
Seniority level: Mid‑Senior level
Employment type: Full‑time
Job function: Finance and Sales
Industries: Hospitals and Health Care
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Company Culture
Everyone is focused on serving the customer and we do that by collaborating and supporting each other
Associates look forward to coming to work each day
Every associate matters and makes a difference
The Quality & Regulatory Compliance Analyst - CONTRACTOR is an integral role in producing standard compliance data for accreditation and regulatory surveys, internal QRC and Supplier Quality audits and data audits, CAPA effectiveness, as well as normalized and standardized MMD categorization. This position will work directly with the Quality and Regulatory Compliance team, as well as field operations to drive reporting, analysis and data integrity regarding compliance to Accreditation Standards, as well as Federal, State and Local Regulations. The Quality & Regulatory Compliance Analyst leverages large and varied datasets to support compliance initiatives and programs across the organization.
Contractor:
This role is for a Contractor, for a fixed duration of time for 8-12 months, and will be contracted through our third‑party vendor partner agency.
Pay Rate: $35 per hour
Location:
Eastern or Central Time Zone; Indianapolis preferred. Our Central Office is located on the northwest side of Indianapolis.
Relocation is not available for this contract
Immigration sponsorship not available for this contract
Responsibilities Compliance Analytics and Reporting (50%)
Conduct targeted analysis of repair and preventive maintenance data related to QRC internal audits and data audits criteria to ensure compliance to federal, state and local regulations and accreditation standards
Compile data and perform analysis for equipment make/models/description and modalities, as well as equipment risk to ensure standardized MMD creation, maintenance and improvement
Support Quality and Regulatory Specialists with reporting criteria and analysis of effectiveness verification post audit and CAPA completion
Identification, monitoring and assistance with risk/opportunity assessment across the organization
Provide oversight, monitoring and analysis with regulatory compliance requirements
Assist with MMD matching of new and existing customer inventory in accordance with TRIMEDX MMD standardization processes and best practices
Conduct analysis and comparison of alerts and recalls in determining impact to TRIMEDX organization and timely closure of loop
Monitor, measure and produce QRC reporting necessary for Quality Management Review on a monthly/quarterly basis
Support Quality and Regulatory Specialists with reporting criteria during site inspections and surveys
QRC Tools, Processes and Program (30%)
Lead QMS internal audit activities (per ISO 13485, 27001 and/or applicable regulatory standards)
Create, manage and monitor PM Transition Plan and Tools for new site implementations and existing sites with PM compliance gaps
Based on data analysis results and organizational feedback, partner with cross‑functional areas when the development of new processes, products, services, or relationships is required
Develop best practices and business rules to ensure uniformity in work, deliverables and outcomes
Assist with creation, analysis and maintaining standardized reporting of Pilgrim CAPA progress and effectiveness verification
Creation, maintenance and improvement of data audit and remote internal audit tool for QRC team and external field‑facing documentation
Participate in AEM (Alternative Equipment Maintenance) and PM Variance Committee by producing pertinent data pull and analysis related to PM Frequency Change and AEM Program requests and speak to outcome of analysis to committee members to drive decision‑making processes related to equipment risk and PM frequencies
Monitor, measure and communicate compliance gaps and risks in a timely manner to ensure mitigation of risks to patient safety and compliance
Demonstrate competency as a QRC subject matter expert for RSQ and QMS software program analysis
Assist with prompt response and actions related to QRC ServiceNow requests (PM Frequency Changes, PM Not Needed Requests, AEM Program Review, Bulk QRC requests)
Communication and Interactions (20%)
Collaborate with cross‑functional business leaders to capture and document QRC reporting and analytics needs
Create and deliver QRC presentation data support and communications to peers, functional area leaders, and executives
Collaborate with QRC team and Field Operations to ensure timely deliverables requested on behalf of surveyor during regulatory and accreditation survey process
Participate in PM Variance and AEM Committees to share QRC analysis with group to drive outcomes based upon compliance
All other duties as assigned.
Skills And Experience
Minimum of 3 years of experience in clinical engineering, quality, compliance, with demonstrated competency in data analysis, reporting, and application of problem solving
Experience with complex reporting and analysis to ensure QRC data integrity and compliance
Strong demonstrated proficiency with Microsoft Office applications; advanced skills with Advanced Excel and Access required (Sequel, Qlik, Tableau experience a plus)
Basic knowledge and application of ISO 13485, 9001 and/or 27001 standards and applicable regulations
Knowledge of healthcare industry, regulatory compliance, clinical engineering, medical technology, and/or healthcare support services preferred
Knowledge of ISO 9001, 13485 and/or 27001 preferred
Strong analytical and interpretation skills to understand complex regulations and data analysis related to compliance
Strong written and verbal communication skills supporting interactions with personnel at all levels within the organization
Creative thinker with ability to meet stringent and changing deadlines with accuracy
Change management and customer focused
Education And Qualifications
Associate's degree in Quality and/or Regulatory Compliance, Clinical Engineering, Applied Science or Business equivalent or equivalent experience required.
Bachelor’s degree preferred.
At TRIMEDX, we are committed to cultivating a workplace culture where every associate feels valued, supported, and empowered to thrive. This culture reflects our belief that our people are our foundation, their well‑being is essential, and shared success is built through meaningful work, recognition, and opportunities for growth.
We embrace people’s differences which include age, race, color, ethnicity, gender, gender identity, sexual orientation, national origin, education, genetics, veteran status, disability, religion, beliefs, opinions and life experiences.
Visit our website to view our Workplace Culture Commitment, along with our social channels to see what our team is up to: Facebook, LinkedIn, Twitter.
TRIMEDX is an Equal Opportunity Employer. Drug-Free Workplace.
Because we are committed to providing a safe and productive work environment, TRIMEDX is a drug‑free workplace. Accordingly, Associates are prohibited from engaging in the unlawful manufacture, sale, distribution, dispensation, possession, or use of any controlled substance or marijuana, or otherwise being under the influence thereof, on all TRIMEDX and Customer property or during working/on‑call hours.
Job Details
Seniority level: Mid‑Senior level
Employment type: Full‑time
Job function: Finance and Sales
Industries: Hospitals and Health Care
#J-18808-Ljbffr