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Merz North America

BioProcess Engineer II

Racine, WI · On-site

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 ...

Merz North America

IT/OT Solutions Analyst

Racine, WI · On-site

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 ...

Info Way Solutions

Warehouse Associate INT

Sturtevant, WI · On-site

$15 - $18/hr

Merz Worker is responsible for all aspects of warehouse functions including the receiving, picking, packing, shipping and preparing of product for customer delivery while maintaining the warehouse in ...

CGS Immersive

Desktop Support Specialist

Raleigh, NC · On-site

Some travel to other Merz facilities may be required. Responsibilities: * Provide onsite Level 2 support for desktops, laptops, peripherals, telephony, mobile devices, and collaboration technologies ...

CGS Immersive

Desktop Support Specialist

Raleigh, NC

Some travel to other Merz facilities may be required. Responsibilities: * Provide onsite Level 2 support for desktops, laptops, peripherals, telephony, mobile devices, and collaboration technologies ...

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As of Jun 27, 2026, the average hourly pay for merz in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What types of tasks and daily activities could I expect as a Merz?

Since "Merz" is not a widely recognized job title in professional listings, daily tasks and activities may vary greatly depending on the specific industry or company context. If you are considering a role titled "Merz," we recommend reviewing the detailed job description or reaching out directly to the employer for clarification on expectations and responsibilities. This will help you better understand the role's scope, core duties, and how you would interact with clients or team members. Being proactive in clarifying the job particulars will help ensure the opportunity aligns with your skills and career goals.

What is a Merz job?

A Merz job typically refers to a position at Merz, a global company specializing in aesthetics, neurotoxins, and dermatology. Merz offers roles in research, sales, marketing, and medical science, among others. Employees often work on developing and promoting medical and aesthetic solutions. The company values innovation, customer focus, and long-term relationships within the healthcare industry. Specific job responsibilities vary based on the role and department.

What are the key skills and qualifications needed to thrive in the Merz position, and why are they important?

It appears that "Merz" is not a commonly recognized professional job title in current real-world employment fields. Without a clear industry context or established role definition, it is not possible to accurately determine the core skills, qualifications, or requirements for this position. Proficiency in industry-relevant tools, certifications, or systems cannot be specified without additional job clarification. Clear communication, adaptability, and teamwork are important for most professional roles, but more information about "Merz" would be needed to provide a tailored skills summary.

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Merz jobs near you
Infographic showing various Merz job openings in the United States as of June 2026, with employment types broken down into 82% Full Time, and 18% Part Time. Highlights an 100% Physical job distribution, with an average salary of $54,791 per year, or $26.3 per hour.
BioProcess Engineer II

BioProcess Engineer II

Merz North America

Racine, WI • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 29 days ago

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.
A Brief Overview
The BioProcess Engineer II leads the development, optimization, and support of manufacturing processes and equipment within a regulated medical device environment. This role manages process and equipment implementation projects, contributes to scale up efforts and continuous improvement activities, and supports production reliability across manufacturing operations. Responsibilities include process design, validation activities, troubleshooting, and collaboration with cross functional partners to ensure products and equipment meet performance, quality, and safety requirements, along with advancing ongoing efforts to refine and strengthen manufacturing processes. The engineer may also support automation initiatives involving robotics, vision systems, or controls programming. Success is measured through effective project execution, adherence to budgets and timelines, and contributions to long term manufacturing capability and reliability.
What You Will Do
  • Process design and implementation: Lead the development and introduction of new manufacturing equipment and processes, including project scoping, budgeting, vendor engagement, and creation of required documentation such as qualification, verification, and validation protocols.
  • Process support and issue resolution: Identify and address production interruptions, perform root cause analysis, develop corrective and preventive actions, and determine calibration and maintenance needs for new and existing equipment to maintain stable and reliable manufacturing operations.
  • Process evaluation and optimization: Establish product and equipment specifications, develop standard operating procedures, assess production costs, and identify opportunities to improve efficiency, throughput, and overall process capability.
  • Project management: Create and maintain project timelines, manage budgets, and drive progress to meet departmental and organizational goals.
  • Cross functional support: Partner with production, quality, engineering, and supplier teams to support daily operations, technology transfer activities, and improvement initiatives.
  • Automation support: Assist in planning or executing automation activities by contributing to or owning projects involving robotics, vision systems, or controls where such technology supports process improvements or equipment upgrades.
  • General support: Provide engineering support as subject matter expert across departments as requested by stakehlders and management to contribute to a culture focused on safety, quality, and continuous improvement.

Minimum Requirements
  • Bachelor of Science (B.S.) in Biomedical Engineering, Mechanical Engineering, Chemical Engineering, or Physical Science
  • 3-5 years of engineering experience in manufacturing, product development, or process development within a regulated industry such as medical devices, pharmaceuticals, or similar.
  • Demonstrated experience supporting or leading process development activities, including verification, validation (IQ/OQ/PQ/PPQ), and technical documentation.
  • Hands-on experience troubleshooting and sustaining manufacturing equipment and production processes in a commercial manufacturing setting.
  • Experience contributing to or leading cross-functional engineering projects with defined timelines and deliverables.

Preferred Qualifications
  • Master of Science (M.S. or M.Sc.) Engineering, Business, or related discipline
  • Experience supporting automation related activities such as robotics integration, vision systems, or industrial controls.
  • Experience with PLC or HMI programming, or working with automation vendors or system integrators.
  • Experience executing or supporting process validation including IQ, OQ, PQ, and PPQ.
  • Experience developing or improving electromechanical or automated manufacturing processes.
  • Familiarity with ISO 13485, FDA QSR, GMP, or other regulated quality system requirements.
  • Experience managing external equipment suppliers, contractors, or integrators.

Technical & Functional Skills
  • Ability to formulate program strategy, budgets and timelines
  • Understanding of process validation, and statistical analysis
  • Familiar with project management methods and tools
  • Solid works or other CAD experience
  • Understanding and application of ISO Quality System requirements and FDA regulations
  • Familiar with a variety of manufacturing processes including mechanical and electromechanical
  • Practical knowledge of Six Sigma methodologies. Green or Black Belt certification
  • Strong technical and problem-solving skills
  • Ability to communicate and write effectively
  • Emotional self-management in difficult situations
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!
This position is not eligible for employer-sponsored work authorization. Applicants must be legally authorized to work in the United States without the need for current or future employer-sponsored work authorization.
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.

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