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Freelance Quality Engineer Fda Jobs in Appleton, WI

... FDA regulated devices. * Lead development and execution of product design strategy to deliver ... and engineering, quality, testing facilities, market research, marketing, and product supply.

Lab Technician

New Holstein, WI · On-site

$23 - $23.60/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Degree in the Sciences or 1+ years of Quality Lab Experience within FDA regulated industry. * Good ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Leadership Development Program (BOLD)

De Pere, WI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Supporting management and quality with complaints, root cause analysis and corrective action ... Learning government regulation and how they relate to Belmark (OSHA, EPA, FDA, etc) Great benefits ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

Showing results 21-40

Freelance Quality Engineer Fda information

See Appleton, WI salary details

$43.9K

$82K

$116.1K

How much do freelance quality engineer fda jobs pay per year?

As of Aug 19, 2026, the average yearly pay for freelance quality engineer fda in Appleton, WI is $81,999.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,300.00 and $90,700.00 per year, depending on experience, location, and employer.

What does a freelance quality engineer FDA do?

A Freelance Quality Engineer FDA is a professional who works independently to help companies comply with FDA regulations, particularly in industries like medical devices, pharmaceuticals, and biotechnology. They are responsible for ensuring that products and processes meet all quality and safety standards set by the FDA. Their tasks may include auditing, creating and reviewing documentation, implementing quality management systems, and assisting with regulatory submissions. By working on a contract basis, they provide specialized expertise to organizations that may not require a full-time quality engineer.

What are the key skills and qualifications needed to thrive as a freelance quality engineer FDA?

To thrive as a Freelance Quality Engineer FDA, you need a solid background in quality assurance, regulatory compliance, and FDA guidelines, often supported by a degree in engineering or life sciences. Familiarity with tools such as quality management systems (QMS), CAPA software, and experience with ISO 13485 or similar certifications is crucial. Strong analytical thinking, attention to detail, and effective communication skills set top professionals apart in this field. These competencies are essential for ensuring product safety, regulatory adherence, and maintaining client trust in the highly regulated medical device and pharmaceutical industries.

What are some common challenges faced by freelance quality engineers working with FDA-regulated products?

Freelance Quality Engineers working in FDA-regulated environments often encounter challenges such as staying up-to-date with evolving FDA regulations, ensuring thorough documentation for audits, and quickly adapting to each client's unique quality management systems. They may also face tight project timelines and the need to communicate effectively with cross-functional teams, including regulatory, manufacturing, and R&D personnel. Building strong relationships and maintaining clear, consistent documentation are essential strategies for overcoming these challenges and delivering successful project outcomes.

What is the difference between Freelance Quality Engineer Fda vs Freelance Quality Assurance Specialist?

AspectFreelance Quality Engineer FdaFreelance Quality Assurance Specialist
CertificationsFDA regulations, ISO standards, QA certificationsISO standards, QA certifications, industry-specific credentials
Work EnvironmentMedical device, pharmaceutical, biotech industriesManufacturing, software, consumer products industries
Employer & Industry UsageRegulated industries requiring FDA complianceVarious industries focusing on quality processes
Common Search & Comparison IntentUnderstanding FDA-specific quality rolesComparing QA roles across industries

Freelance Quality Engineer Fda primarily focuses on ensuring compliance with FDA regulations in regulated industries like pharmaceuticals and medical devices. Freelance Quality Assurance Specialist covers broader quality assurance tasks across various sectors. While both roles require QA certifications, the FDA-specific role emphasizes regulatory knowledge, making it ideal for those targeting FDA-regulated industries.

What are popular job titles related to Freelance Quality Engineer Fda jobs in Appleton, WI?

For Freelance Quality Engineer Fda jobs in Appleton, WI, the most frequently searched job titles are:

What job categories do people searching Freelance Quality Engineer Fda jobs in Appleton, WI look for?

The top searched job categories for Freelance Quality Engineer Fda jobs in Appleton, WI are:

What cities near Appleton, WI are hiring for Freelance Quality Engineer Fda jobs?

Cities near Appleton, WI with the most Freelance Quality Engineer Fda job openings:

Lead Scientist Product

Kimberly-Clark

Neenah, WI • On-site

Full-time

Retirement

Re-posted 8 days ago


Kimberly-Clark rating

8.5

Company rating: 8.5 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

32nd of 540 rated manufacturers


Job description

Lead Scientist ProductJob Description

Join the team behind iconic brands like Huggies, Kleenex, Cottonelle, Scott, Kotex, Poise, Depend, and Kimberly-Clark Professional. At Kimberly-Clark, it's all here for you-innovation, growth, and the chance to make a real impact.

You were made to create Better Care for a Better World: exploring uncharted questions, engineering innovative solutions, advancing scientific understanding, and constantly pushing the boundaries of what's possible. You want to be part ofa performance culture dedicated to solving real-world problems with purpose and precision. You want to work in an environment that promotes sustainability, inclusion, wellbeing, and career development. In this role, you'll help us shape the future and improve lives for billions of people around the world.

It starts with YOU.

This position reports into the Global R&D Class II Tampon Team. The incumbent will have primary accountabilities for product development activities for U by Kotex product variants with focus on, but not limited to, tampons and regulated devices, spanning innovation, development and commercialization, through post market surveillance. Previous experience in product development or research or quality management is preferred.

Candidates who want to broaden their perspective and capabilities through working on a regulated business will find this position highly rewarding.

About You

In one of our R&D, roles, you'll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center. Job responsibilities include:

  • Lead product development efforts for multiple projects and initiatives across the range of product development cycle. This spans from early Front End Innovation, development and commercialization, through post market surveillance.
  • Develop mastery in and adhere to Design and Document Control processes and principles, as required in the development and support of FDA regulated devices.
  • Lead development and execution of product design strategy to deliver desired consumer benefits while ensuring alignment with Vision/Migration plans.
  • Lead development of product key milestones, budget, timeline, and resource forecast for assigned project(s).
  • Ensure development and execution of product specification and quality plans appropriate for phase of project.
  • Manage development and lead execution of learning plan in conjunction with Marketing Research and Innovation Testing teams.
  • Facilitate discussions with marketing and the design team regarding claims and aesthetics.
  • Plan and carry out project responsibility with limited assistance and direction.
  • Communicate and document project plans and results to key customers.
  • Develop knowledge and skills to be recognized as an effective implementer of research principles, scientific analysis, and project management.
  • Seek, recognize, define, and solve problems to achieve unit objectives. Identify complex technical issues to determine root cause, develop and recommend solutions.
  • Build mastery of medical device product development principles and test methods and apply them successfully on development projects.

It starts with YOU. To succeed in this role, you will need the following qualifications:

  • Candidates must possess a bachelor's or advanced degree in related major scientific or engineering discipline from an accredited college or university. May also include other relevant disciplines
  • 5+ years of experience in a variety of technical or operational assignments.
  • Knowledge and background in product development, including associated tools and methodologies. A demonstrated ability to translate that knowledge into execution of process or product related initiatives.
  • Working knowledge and/or direct experience with Design and Document Control processes and principles, as required in the development and support of FDA regulated devices is preferred.
  • Proven ability to work effectively independently or with multiple functions in a project team, such as: legal, safety, regulatory, external design and engineering, quality, testing facilities, market research, marketing, and product supply.
  • Ability to travel up to 25% domestic and international.

Led by Purpose. Driven by You.

Total Benefits

We believe that our employees are our greatest asset, and we're committed to providing them with the resources they need to be successful. If you're looking for a rewarding career with a company that cares about its employees, then Kimberly-Clark is the place for you.

Here are just a few of the benefits you'd enjoy working in this role for Kimberly-Clark. For a complete overview, see www.mykcbenefits.com

Flex That Works at Kimberly-Clark
We believe great work happens when people come together with purpose. That's why we offer a flexible work model that blends remote work with intentional in-person collaboration - helping you connect, grow, and innovate while maintaining the balance you value.

To Be Considered
Click the Apply button and complete the online application process. A member of our recruiting team will review your application and follow up if you seem like a great fit for this role.

In the meantime, please check out the careers website.

And finally, the fine print....


For Kimberly-Clark to grow and prosper, we must be an inclusive organization that applies the diverse experiences and passions of its team members to brands that make life better for people all around the world, which is why we seek to build a workforce that encompassesthe experiences of our consumers.When you bring your original thinking to Kimberly-Clark, you fuel the continued success of our enterprise. We are a committed equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, age, pregnancy, genetic information, citizenship status, or any other characteristic protected by law.

The statements above are intended to describe the general nature and level of work performed by employees assigned to this classification. Statements are not intended to be construed as an exhaustive list of all duties, responsibilities and skills required for this position.

Employment is subject to verification of pre-screening tests which may include drug screening, background check,and DMV check.

Veterans and members of the Reserve and Guard are highly encouraged to apply.

At Kimberly-Clark, pay is just one aspect of our total rewards package, which also includes a variety of benefits and opportunities to achieve, thrive and grow. Along with base pay, this position is eligible for overtime pay and a comprehensive benefits suite, including our 401(k) and Profit-Sharing plan. The anticipated base pay range for this role is provided above for a fully qualified hire. Actual pay will depend on several factors, such as location, role, skills, performance, and experience. Please note that the stated pay range applies to US locations only.

Kimberly-Clark will support in-country relocation for the chosen candidate for the role. The benefits provided will be per the terms of Kimberly-Clark's applicable mobility policies.The benefits/policy provided will be decided at Kimberly-Clark's sole discretion.

This is a P/2 Grade 10 and compensation may vary based on location.

#LI-Hybrid

Salary Range: 87,260 - 107,780 USDAt Kimberly-Clark, pay is just one aspect of our total rewards package, which also includes a variety of benefits and opportunities to achieve, thrive and grow. Along with base pay, this position offers eligibility for a target bonus and a comprehensive benefits suite, including our 401(k) and Profit Sharing plan. The anticipated base pay range for this role is provided above for a fully qualified hire. Actual pay will depend on several factors, such as location, role, skills, performance, and experience. Please note that the stated pay range applies to US locations only.Primary LocationNeenah - West R&E OfficeAdditional LocationsWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

What Kimberly-Clark employees say

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Kimberly-Clark logo

About Kimberly-Clark

Sourced by ZipRecruiter

Huggies®. Kleenex®. Cottonelle®. Scott®. Kotex®. Poise®. Depend®. Kimberly-Clark Professional®. You already know our legendary brands--and so does the rest of the world. In fact, 25% of people in the world use Kimberly-Clark products every day. We know that these amazing Kimberly-Clark products wouldn't exist without skilled workers, like you. Here, you'll use your skills to make some of the most helpful things for billions of people all around the world - all in a safe, stable, and caring environment. While our products support better lives for billions of people around the world, our company passionately supports the ability for over 45,000 employees to do their best work and enjoy life.

Industry

Manufacturing

Company size

10,000+ Employees

Headquarters location

Irving, TX, US

Year founded

1872