ZipRecruiter

Log In

1

Freelance Pharma Quality Assurance Jobs in Decatur, IN

SQA Services

Quality Auditor - Pharmaceutical

Warren, IN · Remote

$1.3K/day

Our associates are expert quality assurance professionals with extensive experience and local ... We're hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform ...

All JobsPharma Quality Assurance JobsFreelance Pharma Quality Assurance JobsFreelance Pharma Quality Assurance Jobs in Decatur, IN

Freelance Pharma Quality Assurance information

See Decatur, IN salary details

$12

$22

$41

How much do freelance pharma quality assurance jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for freelance pharma quality assurance in Decatur, IN is $22.38, according to ZipRecruiter salary data. Most workers in this role earn between $16.92 and $23.41 per hour, depending on experience, location, and employer.

What does a freelance pharma quality assurance professional do?

A Freelance Pharma Quality Assurance (QA) professional works independently to ensure that pharmaceutical products and processes comply with regulatory standards and quality requirements. Their responsibilities include reviewing documentation, conducting audits, validating processes, and identifying areas for improvement in manufacturing and development. They help companies maintain compliance with agencies like the FDA or EMA and can provide expertise on quality systems, risk management, and corrective actions. Freelancers in this role may work with multiple clients, offering flexibility and specialized knowledge for short-term or project-based needs.

What are the key skills and qualifications needed to thrive as a freelance pharma quality assurance professional?

To thrive as a Freelance Pharma Quality Assurance professional, you need a solid background in pharmaceutical regulations, quality management systems, and relevant scientific or engineering qualifications. Familiarity with tools like LIMS (Laboratory Information Management Systems), GMP (Good Manufacturing Practice) standards, and certifications such as ISO 9001 or Six Sigma is highly valued. Strong attention to detail, problem-solving skills, and the ability to communicate effectively with diverse stakeholders set outstanding professionals apart. These skills and qualifications ensure compliance, product safety, and reliable delivery of quality assurance services to pharmaceutical clients.

What are some common challenges faced by freelance pharma quality assurance professionals when working with multiple clients?

Freelance pharma quality assurance professionals often navigate varying company protocols, diverse documentation systems, and unique regulatory requirements across different clients. Juggling multiple projects can require strong organizational skills to ensure all deadlines and compliance standards are consistently met. Additionally, freelancers must quickly adapt to new teams and establish clear communication to effectively address quality issues and implement corrective actions. Building trust and demonstrating expertise are crucial for long-term client relationships in this highly regulated industry.

What is the difference between Freelance Pharma Quality Assurance vs Pharma Quality Control?

AspectFreelance Pharma Quality AssurancePharma Quality Control
CredentialsGMP certifications, QA trainingLab certifications, QC training
Work EnvironmentConsulting, client sites, remoteLaboratories, manufacturing plants
Employer & Industry UsageFreelance/contract basis in pharma industryIn-house or contracted lab roles in pharma

Freelance Pharma Quality Assurance professionals focus on ensuring compliance with regulations and quality systems across various projects, often working remotely or on-site as consultants. Pharma Quality Control roles involve testing and analyzing products directly in labs or manufacturing facilities. While both roles require GMP knowledge, QA emphasizes process oversight, whereas QC centers on product testing. Understanding these differences helps job seekers target the right opportunities in the pharmaceutical industry.

What job categories do people searching Freelance Pharma Quality Assurance jobs in Decatur, IN look for?

The top searched job categories for Freelance Pharma Quality Assurance jobs in Decatur, IN are:

What cities near Decatur, IN are hiring for Freelance Pharma Quality Assurance jobs?

Cities near Decatur, IN with the most Freelance Pharma Quality Assurance job openings:

Freelance Pharma Quality Assurance jobs near you
Infographic showing various Freelance Pharma Quality Assurance job openings in Decatur, IN as of June 2026, with employment types broken down into 4% As Needed, 20% Full Time, 11% Part Time, 28% Contract, and 37% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $46,541 per year, or $22.4 per hour.

Quality Auditor - Pharmaceutical

SQA Services

Fort Wayne, IN • Remote

$1.3K/day

Full-time

Posted 27 days ago

Job description

For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across all industries. We deliver these services by deploying a network of highly skilled associates based throughout the United States and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our competitors.
 
We're hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform supplier quality  audits at various suppliers in the Midwest. These audits are generally 1-2 days long. You are given the flexibility to accept or reject these assignments according to your own availability. 
Key Responsibilities
  • Perform supplier audits at various sites within your region of residence
  • Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries
  • Coordinate, prepare, execute, and deliver supplier audits based on your own and the client schedule
  • Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc...
  • Respond to the Content team in a timely manner regarding edits/questions to your audit report
  • Write audit reports in accordance with client specifications
Required Qualifications
  • 5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries
  • Has been the lead auditor in at least 10 audits
  • Direct audit experience to 21 CFR part 210/211, EU Vol 4, and Canada GMP
  • Strong communication and writing skills
  • Proven ability to deescalate workplace conflicts effectively
  • Ability to adapt to new technology and software.
  • Willingness to travel regionally
Preferred Qualifications
  • Direct audit experience to ISO 17025, ISO 15378, IPEC GDP, ICH Q7, ISO 13485, 21 CFR 100, and/or 21 CFR 507
  • ISO certifications are a plus but not mandatory
$1,300 - $1,300 a day
Pay Rate: 
 
$1300 for a 1-day audit. Includes: Time spent preparing for the audit, traveling, performing the audit, writing the report, and responding to questions from our Content team of editors and the client until the report is finalized. Does not include: Following up on CAPA for any findings or reimbursement for travel expenses - expenses are reimbursed at cost with receipts per SQA travel policy. Note that SQA helps with the preparation of the audit and proofreads all audit reports.
 
Note: SQA is an Equal Opportunity Employer. Employment is based on merit and qualifications, and is not influenced by race, color, religion, gender, national origin, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.
 
#ZR
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job

Apply