Statistical Analysis

Lead Data Scientist | Remote – GA, LA, OK, TN or TX

Location: Remote within Georgia, Louisiana, Oklahoma, Tennessee or Texas

Primary Business Location: Houston, Texas

Work Arrangement: Fully remote within an approved state

Employment Type: Full-time, permanent

Industry: Healthcare and Health Technology

Experience Level: Experienced Individual Contributor / Technical Lead

Reports To: Manager, Data Science

Base Salary: $143,000–$180,000

Travel: Up to 20%

Relocation Assistance: Not available

Visa Sponsorship: Limited sponsorship may be considered

Position Overview

A leading healthcare organization is seeking an experienced Lead Data Scientist to lead high-priority analytical projects and solve complex organizational challenges using advanced statistical analysis, machine learning, predictive modeling and data visualization.

This is a hands-on technical leadership position. The successful candidate will remain actively involved in data exploration, model development, testing and interpretation while guiding projects, partnering with internal customers and mentoring other data scientists.

Key Responsibilities

• Lead analysis of complex structured and unstructured datasets.

• Develop, test, validate and maintain machine-learning and predictive models.

• Apply regression, time-series forecasting, classification, clustering, decision trees, neural networks, A/B testing and hypothesis testing.

• Evaluate model accuracy, stability, interpretability and fitness for purpose.

• Document methodologies, assumptions, limitations and validation results.

• Research and resolve data-quality problems across incomplete or inconsistent sources.

• Build repeatable analytical processes and production-ready solutions.

• Translate complex findings into clear recommendations for technical teams, business leaders and executives.

• Lead projects from discovery through modeling, implementation and measurement.

• Mentor data scientists and raise technical standards across the team.

• Partner with engineering, analytics, clinical and operational stakeholders.

• Support responsible and practical use of advanced analytics within healthcare.

Required Qualifications

• Advanced degree or equivalent experience in data science, statistics, mathematics, computer science, engineering, economics or a related quantitative discipline.

• Extensive professional data-science and advanced-analytics experience.

• Expert knowledge of statistical analysis, machine learning and predictive modeling.

• Strong programming experience using Python, R, SQL or comparable tools.

• Experience working with large, complex datasets and resolving data-quality issues.

• Ability to explain sophisticated concepts clearly to non-technical audiences.

• Strong project leadership, consulting and stakeholder-management skills.

• Ability to remain hands-on while leading technical delivery.

• Residence in Georgia, Louisiana, Oklahoma, Tennessee or Texas.

Preferred Qualifications

• Healthcare or health-technology experience.

• Experience deploying and monitoring models in production environments.

• Cloud analytics, distributed-computing or big-data experience.

• Experience mentoring technical professionals and leading cross-functional projects.

• Knowledge of data governance, privacy and responsible AI practices.

Equal Opportunity

The organization is an Equal Opportunity Employer and considers qualified applicants without discrimination based on any status protected by applicable law.

Senior Analyst, Workforce Analytics | Remote – GA, LA, OK, TN or TX

Location: Remote within Georgia, Louisiana, Oklahoma, Tennessee or Texas

Primary Business Location: Houston, Texas

Work Arrangement: Fully remote within an approved state

Employment Type: Full-time, permanent

Industry: Healthcare

Experience Level: Senior

Reports To: Director, Workforce Analytics

Base Salary: $90,000–$110,000

Travel: Up to 20%

Relocation Assistance: Not available

Visa Sponsorship: Not available

Position Overview

A leading healthcare organization is seeking a highly analytical and consultative Senior Analyst, Workforce Analytics to transform complex workforce data into meaningful insights, recommendations and business decisions.

This is a hands-on analytics position. The successful candidate will partner with HR, Finance, Technology and operational leaders to understand the business problem behind each request, challenge assumptions, identify root causes and independently determine the most effective analytical solution.

Key Responsibilities

• Conduct complex analyses across headcount, turnover, retention, recruitment, compensation, diversity, productivity and organizational data.

• Translate undefined workforce challenges into structured analytical plans.

• Identify trends, relationships, risks and opportunities within large datasets.

• Develop dashboards, reports, data visualizations and executive-ready presentations.

• Apply statistical techniques and predictive methods to workforce questions.

• Combine data from multiple systems and improve data quality, definitions and governance.

• Partner with HR, Finance, IT and business leaders to define metrics and interpret results.

• Explain what is happening, why it matters and what action should be considered.

• Present findings clearly to senior leaders and non-technical stakeholders.

• Support workforce planning, talent strategy and operational decision-making.

• Manage several analytical projects and priorities independently.

• Mentor colleagues and help improve analytics standards and practices.

Required Qualifications

• Bachelor’s degree in analytics, statistics, mathematics, economics, business, HR, computer science or a related discipline.

• Significant professional experience in workforce, people, HR or business analytics.

• Strong analytical, statistical and problem-solving capability.

• Experience working with large, complex and imperfect datasets.

• Advanced Excel skills and experience with SQL, data visualization and reporting tools.

• Ability to create clear business narratives from analytical findings.

• Strong consulting, stakeholder-management and presentation skills.

• Ability to work independently in an ambiguous, fast-moving environment.

• Residence in Georgia, Louisiana, Oklahoma, Tennessee or Texas.

• Current authorization to work in the United States without sponsorship.

Preferred Qualifications

• Healthcare-industry experience.

• Experience with Tableau, Power BI or comparable visualization platforms.

• Knowledge of HRIS, workforce-planning or talent-management data.

• Experience with predictive analytics, statistical programming or data modeling.

• Graduate degree in a quantitative or business discipline.

Equal Opportunity

The organization is an Equal Opportunity Employer and considers qualified applicants without discrimination based on any status protected by applicable law.

Industrial Engineer III (Packaging) – Manufacturing, SAP, Lean, Material Flow | Eagle, WI

Industrial Engineer III – Packaging

📍 Location: Eagle, Wisconsin (Onsite)
💼 Employment Type: Full-Time
🎓 Education: Bachelor’s Degree required (Engineering or Industrial Technology)
📈 Experience Level: Mid-Senior
🕒 Experience Required: 5–7+ years
🌎 Visa Sponsorship: Not available
🚚 Relocation Assistance: Not available
✈️ Travel: ~10% (occasional regional travel)

Role Overview

We are seeking an experienced Industrial Engineer III (Packaging) to lead the development and optimization of supplier packaging and material presentation strategies for manufacturing operations.

This role is critical in ensuring efficient material flow, cost optimization, and protection of components during transit, working closely with cross-functional teams across engineering, supply chain, logistics, and manufacturing.

Key Responsibilities

Packaging Strategy & Optimization

  • Develop and implement supplier packaging standards and policies

  • Design packaging solutions to protect materials during transport and handling

  • Create packaging models supporting:

    • Plan for Every Part (PFEP)

    • Total Cost of Ownership (TCO)

  • Establish monitoring systems to ensure supplier compliance

Continuous Improvement & Operational Excellence

  • Lead continuous improvement initiatives to enhance efficiency and reduce costs

  • Optimize material flow, layouts, and processes to improve operational performance

  • Implement lean principles and demand-driven strategies (flexibility, speed, responsiveness)

  • Identify and drive innovative solutions to improve business outcomes

Cross-Functional Collaboration

  • Partner with engineering, quality, supply chain, logistics, and manufacturing teams

  • Work closely with shop floor personnel to improve processes and systems

  • Support new product introduction (NPI) by ensuring correct packaging specifications

Process Development & Documentation

  • Develop and validate:

    • Standard Operating Procedures (SOPs)

    • Work Instructions

    • Test methods and capability studies

  • Provide training and guidance on packaging processes

  • Ensure proper material preservation standards for service requirements

Supplier & Material Flow Management

  • Travel to supplier locations to assess inbound material handling and packaging needs

  • Design processes for inter-facility material transfers (e.g., sheet metal components)

  • Ensure materials arrive production-ready (paint, storage, assembly, etc.)

Required Qualifications

  • Bachelor’s degree in Engineering or Industrial Technology

  • 5+ years of experience in manufacturing or industrial engineering environments

  • Experience with process improvement and material flow optimization

  • Strong analytical and problem-solving capabilities

  • Excellent communication and cross-functional collaboration skills

Preferred Qualifications

  • Experience with ERP systems (SAP / SAP Business Objects)

  • Proficiency in CAD tools (AutoCAD, SolidWorks, ProE)

  • Knowledge of lean manufacturing principles

  • Experience in high-mix/low-volume and high-volume/low-mix environments

  • Background in project management (certification preferred)

  • Experience in training, coaching, or mentoring teams

  • Strong statistical analysis skills

Ideal Candidate

The ideal candidate is a hands-on industrial/packaging engineer who:

  • Has strong experience in material handling and supplier packaging design

  • Understands manufacturing environments and inter-facility logistics

  • Can develop practical, scalable packaging solutions (not consumer packaging)

  • Is comfortable working both strategically and on the shop floor

  • Has experience creating processes to protect industrial components in transit

  • Thrives in a fast-paced, cross-functional environment

Physical Requirements

  • Regular standing, walking, and use of hands

  • Occasional lifting (25–50 lbs)

  • Periods of computer-based work

  • Occasional bending, reaching, and shop floor activity

Benefits

  • Comprehensive benefits package

  • Health, dental, and vision coverage

  • Retirement plans

  • Paid time off

  • Additional employee benefits

Screening Questions

  • Can you describe your experience with material planning, packaging, and delivery workflows?

  • Have you created work instructions or SOPs for packaging or manufacturing processes?

  • What experience do you have with ERP systems (e.g., SAP)?

  • How have you collaborated with production teams to improve processes?

  • What is driving your interest in a new opportunity?

 

Senior Software Quality Engineer – Medical Devices | Limerick, IRE

Senior Software Quality Engineer

📍 Location: Limerick, Ireland
🏢 Work Model: Hybrid – Minimum 4 days onsite
💼 Employment Type: Full-Time
💰 Salary: €60,000 – €70,000
✈️ Travel: Occasional
🎓 Education: Bachelor’s Degree in Engineering or related technical field

Role Overview

A leading global medical technology organization is seeking a Senior Software Quality Engineer to support research and development programs focused on innovative medical technologies.

This role will be responsible for establishing and maintaining software quality processes, regulatory compliance, and design control systems to ensure the successful development and delivery of high-quality medical device software.

The position plays a key role in new product development, manufacturing transfer, and quality management system implementation, ensuring software systems meet both regulatory standards and customer expectations.

Key Responsibilities

Software Quality & Compliance

  • Develop and maintain software quality strategies, processes, and procedures

  • Ensure compliance with medical device regulatory standards including:

    • FDA 21 CFR Part 820

    • FDA 21 CFR Part 11

    • ISO 13485

    • ISO 14971

    • IEC 62304

    • EU MDR 2017/745

  • Guide computer system validation (CSV) and electronic records compliance

Design & Development Quality

  • Support software lifecycle activities including:

    • Requirements management

    • Software development planning

    • Risk management

    • Verification & validation (V&V)

  • Facilitate design reviews and functional reviews

  • Review and approve technical documentation including:

    • Design documentation

    • Verification and validation protocols

    • Product drawings

Cross-Functional Collaboration

  • Represent the Quality function within New Product Development teams

  • Work closely with R&D, manufacturing, and engineering teams

  • Support technology transfer initiatives between development and manufacturing environments

Continuous Improvement & Quality Systems

  • Contribute to the development and implementation of quality management systems

  • Support CAPA investigations and remediation activities

  • Drive improvements in test coverage, software reliability, and system performance

Data Analysis & Problem Solving

  • Apply statistical tools and quality methodologies to:

    • Identify root causes

    • Analyse product or process issues

    • Implement corrective actions

Required Qualifications

  • Bachelor’s degree in:

    • Software Engineering

    • Electrical Engineering

    • Biomedical Engineering

    • Mechanical Engineering

    • Or a related technical discipline

  • 6–7 years of professional experience in engineering or quality roles

  • At least 4+ years of experience in software development lifecycle or software quality

  • Strong understanding of medical device regulatory requirements

  • Experience with:

    • Software validation

    • Design controls

    • Risk management processes

  • Strong analytical, problem-solving, and communication skills

Preferred Experience

  • Experience in medical devices, healthcare technology, or regulated environments

  • Familiarity with CAPA processes and audit remediation

  • Knowledge of:

    • Six Sigma methodologies

    • Root cause analysis tools

    • Statistical sampling techniques

  • Experience working on cross-functional product development teams

Ideal Candidate

The ideal candidate is a software quality specialist within regulated industries who:

  • Has strong experience in medical device software compliance

  • Understands design controls and validation processes

  • Can support new product development programs

  • Works effectively with cross-functional engineering teams

  • Applies structured problem-solving and quality methodologies

Why Join

  • Opportunity to work on cutting-edge medical technologies

  • Collaborative engineering and research environment

  • Work with global teams driving healthcare innovation

  • Strong culture of professional growth and technical excellence

 

Senior Quality Engineer – Design Assurance | Medical Devices | Limerick, Ireland

Senior Quality Engineer – Design Assurance

📍 Location: Limerick, Ireland
🏢 Work Model: Hybrid – Minimum 4 days onsite
💼 Employment Type: Full-Time
💰 Salary: €60,000 – €70,000
✈️ Travel: Occasional
🎓 Education: Bachelor’s Degree in Engineering or related discipline preferred

Role Overview

A global medical technology organization is seeking a Senior Quality Engineer – Design Assurance to support new product development and sustaining engineering projects.

In this role, you will act as the Quality representative on cross-functional project teams, ensuring that products meet global regulatory requirements and internal quality standards throughout the entire product lifecycle—from concept and development through product launch and ongoing support.

You will play a critical role in design controls, risk management, verification & validation, and regulatory compliance, helping deliver high-quality medical technologies that improve patient care.

Key Responsibilities

Design Assurance & Product Development

  • Represent the Quality function on project core teams for new product development and design change projects

  • Support product lifecycle activities from concept through launch and maintenance

  • Ensure compliance with design control, risk management, and change control processes

Risk Management & Compliance

  • Lead risk management activities throughout the product development lifecycle

  • Support compliance with key standards such as:

    • ISO 13485

    • ISO 14971

    • IEC 60601

    • IEC 62304

    • EU MDR

  • Ensure regulatory requirements are integrated into development activities

Verification & Validation

  • Support development and execution of verification and validation (V&V) strategies

  • Review and approve test plans, protocols, and reports

  • Evaluate statistical approaches and challenge testing methodologies where necessary

  • Authorise and assess deviations during testing activities

Documentation & Quality Systems

  • Contribute to the creation and maintenance of Design History File (DHF) documentation

  • Support Quality Management System (QMS) activities including:

    • CAPA investigations

    • Field assessments

    • Operational engineering evaluations

  • Ensure accurate documentation and traceability across development programs

Issue Management & Continuous Improvement

  • Support failure investigations and root cause analysis

  • Manage software issue tracking in accordance with IEC 62304

  • Promote a strong quality culture across project teams

Required Qualifications

  • Bachelor’s degree in Engineering or related technical discipline
    (Equivalent experience considered)

  • Minimum 5+ years of experience in Quality Engineering within a regulated environment

  • Strong knowledge of:

    • ISO 13485

    • QSR / FDA quality requirements

    • ISO 14971 risk management

    • Statistical analysis techniques

  • Experience with:

    • Design assurance processes

    • Design controls and change control

    • Risk management methodologies

  • Strong written and verbal communication skills

  • Ability to manage multiple projects and priorities simultaneously

Preferred Experience

  • Experience with EU Medical Device Regulation (MDR)

  • Knowledge of:

    • IEC 62304 (medical device software lifecycle)

    • IEC 62366 (usability engineering)

  • Experience supporting software-enabled medical devices

  • Experience working with cross-functional product development teams

Ideal Candidate

The ideal candidate is a Quality Engineer experienced in regulated product development who:

  • Has strong expertise in design assurance and risk management

  • Understands the medical device regulatory landscape

  • Can effectively influence cross-functional engineering teams

  • Demonstrates strong attention to detail and analytical thinking

  • Promotes a patient-first approach to quality and compliance