Senior Manager Quality Engineering-Labeling

Merz Aesthetics; Franksville (WI); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Medical, Dental, and Vision

PTO 20 days

Paid holidays

Paid Sick Leave

Parental leave

401(k)

Employee bonuses

Job summary

Merz Aesthetics, a leader in global aesthetics, is seeking a labeling quality leader in Wisconsin to drive compliance, lifecycle management, and cross-functional collaboration across global teams.

You will oversee labeling QA processes, risk management, change control, and inspection readiness, partnering with Regulatory, Manufacturing, and Quality to ensure labeling accuracy and regulatory adherence. The role requires strategic thinking and talent development across the product lifecycle.

Qualifications

• Bachelor of Science in Life Sciences, Engineering, Regulatory Affairs, or related field.
• 5+ years in Quality, Regulatory Affairs, Labeling, or related function in regulated industry.
• 3-5 years leading cross-functional initiatives across multiple functions and levels.
• First leadership experience managing professional staff and developing talent.
• Strong knowledge of labeling regulations and regulatory requirements.

Responsibilities

• Manage labeling QA processes and systems to ensure accuracy, compliance, and consistency.
• Oversee labeling activities including review, approval, document control, risk management, and change control.
• Ensure compliance with regulatory requirements, industry standards, and company policies.
• Develop and implement quality improvement initiatives for labeling procedures.
• Monitor labeling processes with metrics, trend analysis, and quality metrics.
• Collaborate with cross-functional teams to address labeling quality issues and drive timely resolution.
• Support Change Control and Risk Management activities.

Skills

Quality Assurance

Process Improvement

Compliance Management

Cross-Functional Collaboration

Risk Assessment

Project Management

Technical Writing

Data Analysis

Problem Solving

Critical Thinking

Education

Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, or related field

Master's Degree in Physical science, engineering, business, or relevant field

Job description

About Us

Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics.

About Us

Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics.

A Brief Overview

This role is responsible for labeling quality and compliance activities to ensure product labeling meets regulatory requirements, industry standards, and company policies. Oversees Product Labeling and New Markets functions while supporting Risk Management and Change Control processes. Drives continuous improvement, operational excellence, and inspection readiness across multiple teams and geographies.Provides strategic leadership for labeling development, review, approval, and lifecycle management, ensuring labeling accuracy, compliance, and product quality. Partners cross-functionally to support product launches, market expansions, quality initiatives, product changes, and risk assessments while developing talent, resolving complex compliance issues, and strengthening quality systems to support business objectives and patient safety.

What You Will Do

• Manage and oversee labeling quality assurance processes and systems Oversee labeling quality processes and systems to ensure labeling accuracy, compliance, and consistency. Support labeling review, approval, document control, risk management, and change control activities while driving continuous improvement and regulatory compliance.
• Ensure compliance with industry regulations and standards for labeling Ensure labeling activities comply with applicable regulatory requirements, industry standards, and company policies through effective oversight, review, audit support, and continuous process improvement.
• Develop and implement quality improvement initiatives for labeling procedures Drive strategic quality improvement initiatives for labeling processes through process optimization, standardization, performance monitoring, and cross-functional collaboration to improve compliance, operational effectiveness, and inspection readiness.
• Monitor and evaluate labeling processes to ensure accuracy and reliability Provide oversight of labeling process performance through monitoring, trend analysis, and quality metrics to ensure labeling accuracy, reliability, compliance, and continuous improvement across the product lifecycle.
• Collaborate with cross-functional teams to address labeling-related quality issues Lead cross-functional efforts to address complex labeling quality and compliance issues, driving timely resolution, risk mitigation, and sustainable process improvements to support product quality and regulatory compliance.
• Support Change Control and Risk Management Activities Provide support and oversight for risk management and change control processes to ensure effective evaluation of changes, mitigation of risks, and compliance with quality system and regulatory requirements.

Minimum Requirements

• Bachelor of Science (B.S.) Life Sciences, Engineering, Regulatory Affairs, or related technical discipline
• 5+ years Progressive experience in Quality, Quality Engineering, Regulatory Affairs, Labeling, or related functions within a regulated industry (medical device, pharmaceutical, biologic, or combination products).
• 3-5 years Experience leading cross-functional initiatives and influencing business decisions across multiple functions and organizational levels.
• First Leadership experience managing professional staff, developing talent, and leading department or functional objectives.
• Quality Assurance
• Process Improvement
• Compliance Management
• Cross-Functional Collaboration
• Risk Assessment
• Project Management
• Technical Writing
• Data Analysis
• Problem Solving
• Critical Thinking

Preferred Qualifications

• Master's Degree Physical science, engineering, business, or relevant field
• Certification(s) – ASQ Quality Assurance Certified Quality Engineer certification
• Lean Six Sigma Certifications (Yellow Belt, Green Belt, Black Belt) Six Sigma certification (green belt or higher)
• Certification(s) – ASQ Quality Assurance Certified Quality Manager

Technical & Functional Skills

• Expert knowledge of quality systems, quality techniques, regulatory requirements, and quality engineering principles.
• Advanced knowledge of labeling regulations, standards, and global compliance requirements.
• Thorough understanding of Quality System requirements including documentation, records management, change control, CAPA, and risk management.
• Ability to lead complex investigations, root cause analyses, and continuous improvement initiatives.
• Ability to develop and implement quality strategies, policies, and engineering standards.
• Ability to provide leadership, coaching, and development to quality engineering staff.
• Ability to collaborate and influence effectively across global cross-functional teams and senior leadership.
• Ability to make sound business decisions and balance quality, compliance, and operational objectives.
• Experience leading regulatory inspections, audits, and inspection readiness activities.
• ASQ Certification (CQE, CMQ/OE) and/or Lean Six Sigma Certification.

Benefits

• Comprehensive Medical, Dental, and Vision plans
• 20 days of Paid Time Off
• 15 paid holidays
• Paid Sick Leave
• Paid Parental Leave
• 401(k)
• Employee bonuses
• And more!
• Your benefits and PTO start the date you're hired with no waiting period!

Work Authorization & Visa Sponsorship

Applicants must be authorized to work in the United States without the need for employment-based visa sponsorship now or in the future. Merz will not sponsor applicants for U.S. work visa status for this opportunity. No sponsorship is available for any employment-based visas, including but not limited to H-1B, L-1, TN, O-1, E-3, H-1B1, F-1, J-1, OPT, CPT, or any other employment-based visa category.