Senior Manager Quality Engineering-Labeling

Posted 2 Days Ago
Be an Early Applicant
2 Locations
Hybrid
Senior level
Beauty • Pharmaceutical
The Role
Leads labeling quality and compliance activities across products and geographies. Oversees labeling review, approval, document control, change control, risk management, audits, and inspection readiness. Drives process improvement, quality metrics, regulatory compliance, complex investigations, and cross-functional issue resolution. Partners with global teams on launches, market expansions, and product changes while developing quality engineering talent and strengthening quality systems.
Summary Generated by Built In

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.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Skills Required

  • Bachelor of Science degree in life sciences, engineering, regulatory affairs, or a related technical discipline
  • 5+ years of progressive experience in quality, quality engineering, regulatory affairs, labeling, or related functions within a regulated industry
  • 3–5 years of experience leading cross-functional initiatives and influencing business decisions
  • Leadership experience managing professional staff, developing talent, and leading department or functional objectives
  • Quality assurance, process improvement, compliance management, risk assessment, project management, technical writing, data analysis, problem solving, and critical thinking skills
  • Expert knowledge of quality systems, quality techniques, regulatory requirements, and quality engineering principles
  • Advanced knowledge of labeling regulations, standards, and global compliance requirements
  • Understanding of documentation, records management, change control, CAPA, and risk management requirements
  • Experience leading complex investigations, root cause analyses, and continuous improvement initiatives
  • Experience leading regulatory inspections, audits, and inspection readiness activities
  • Master's degree in physical science, engineering, business, or a relevant field
  • ASQ Certified Quality Engineer certification
  • Lean Six Sigma certification at Green Belt level or higher
  • ASQ Certified Quality Manager certification
  • ASQ CQE or CMQ/OE certification
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The Company
HQ: Raleigh, North Carolina
3,064 Employees

What We Do

Merz Aesthetics is a medical aesthetics business with a long history of empowering health care professionals, patients and employees to live every day with confidence. We aim to help people around the world look, feel and live like the best versions of themselves — however they define it. Clinically proven, its product portfolio includes injectables, devices and skin care treatments designed to meet each patient’s needs with high standards of safety and efficacy. Being family owned for more than 115 years, Merz Aesthetics is known for building unique connections with customers who feel like family. Merz Aesthetics’ global headquarters is in Raleigh, N.C., USA, with a commercial presence in 90 countries worldwide. It is also a part of Merz Group, which was founded in 1908 and is based in Frankfurt, Germany. Learn more at merzaesthetics.com.

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