Sr Applications Quality Engineer

Posted 5 Days Ago
Be an Early Applicant
Racine, WI, USA
Hybrid
Senior level
Beauty • Pharmaceutical
The Role
Lead development, implementation, and maintenance of validated quality system applications and data visualization tools. Manage CSV efforts, environments (DEV/QA/Prod), incidents, upgrades, and full software project lifecycles while ensuring GxP and 21 CFR Part 11 compliance and cross-functional stakeholder alignment.
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

Responsible for development, implementation, and maintenance of Quality System applications and data visualization tools. This role will strategically align with business objectives to develop, implement, and optimize digital solutions that enhance operational excellence across quality and manufacturing processes. The role involves collaborating with cross-functional teams to plan, execute, and document CSV efforts, monitor validated systems, conduct periodic reviews, and manage related investigations. This role will ensure system support and maintenance of applicable business applications and data visualization tools are appropriately established. You will work with our business customers to ensure key technologies are delivering required value to the organization.

What You Will Do

  • Ensure application support and management by establishing processes to manage user accounts, permissions, and security policies.

  • Ensure appropriate level of technical assistance is available to users.

  • Ensure process is established to troubleshoot issues and conduct training on new features and system use.

  • Manage the handling of incidents until they are fully resolved, with a detailed analysis of the underlying causes provided.

  • Monitor and maintain these technologies at optimal performance levels.

  • Responsible for gathering requirements and analyzing processes in order to recommend new technologies or improvements existing to quality system applications or data visualization tools.

  • Interpret business requirements to functional designs. Configure and / or partner with external design engineers to configure applications or data visualization tools which align with business requirements.

  • Acts as the principal designer for major systems and their subsystems.

  • Build and maintain multiple DEV, QA and production environments

  • Collaborate with key stakeholder on system upgrades and enhancements. Provide input to create a compelling roadmap for new technology and system upgrades.

  • Create and maintain robust and validated processes for making changes.

  • Lead in the planning, development, and implementation of computer systems validation documentation and ensure compliance with required GxP and 21 CFR Part 11 regulations.
  • Provide input in creation and/or review of internal operating procedures. 
  • Assist in ensuring applicability of current quality policies, procedures and objectives by keeping informed of the latest updates/modifications related to industry standards and federal regulations.
  • Provide support for the Quality Assurance/Operations Departments and to other company departments as directed by Quality Systems Management.

  • Serve as the CSV representative during regulatory inspections.

  • Own the full project lifecycle for software application deployments — from initial scoping through production release — serving as the technical lead and primary escalation point for cross-functional teams.

  • Drive the planning, testing, and implementation of new software capabilities and operational improvements, bringing innovative approaches to complex deployment challenges at the division or business unit level.

  • Manage project scope, budgets, and delivery timelines with rigor, ensuring all milestones are met across directly managed and matrixed teams.

  • Hold accountability for the successful, on-time completion of every task and project under your purview, proactively identifying risks and resolving blockers before they impact delivery.

Minimum Requirements

  • Bachelor's Degree in Computer Science and/or Life Sciences
  • 5+ years of computer software support and/or related experience
  • 5+ Experience in Quality Assurance within medical device/pharma environment and/or related field.
  • Drivers License Upon Hire

Preferred Qualifications

    Technical & Functional Skills

    • Must be proficient in MS Word, Excel, and PowerPoint software programs.
    • Must have excellent verbal and written communication skills and leadership skills.
    • Ability to work with company staff and communicate effectively throughout the organization is essential.
    • Familiar with industry standards and Federal Regulations.
    • Strong understanding of industry standards and best practices for computer computer validation and assurance such as GAMP 5, 21 CFR Part 11, Annex 11, etc.
    • Experience in application configuration.
    • Strong technical writing and general problem-solving skills.
    • Experience with software quality engineering or QA focused on infrastructure, platform, or DevOps environments (qualification and validation).
    • Familiarity with emerging digital technologies and tools, including AI/ML or advanced data visualization platforms, to support process improvement and decision-making.
    • Experience with owning quality strategy across the full SDLC in distributed, cloud-native systems to drive insights and digital innovation initiatives.

    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's Degree in Computer Science and/or Life Sciences
    • 5+ years of computer software support and/or related experience
    • 5+ years of Quality Assurance experience within medical device or pharmaceutical environments
    • Driver's license upon hire
    • Proficiency in Microsoft Word, Excel, and PowerPoint
    • Excellent verbal and written communication and leadership skills
    • Familiarity with industry standards and federal regulations (GxP)
    • Strong understanding of computer system validation best practices (GAMP 5, 21 CFR Part 11, Annex 11)
    • Experience in application configuration
    • Strong technical writing and problem-solving skills
    • Experience with software quality engineering or QA focused on infrastructure, platform, or DevOps environments
    • Familiarity with emerging digital technologies including AI/ML and advanced data visualization platforms
    • Experience owning quality strategy across the full SDLC in distributed, cloud-native systems
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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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