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Remote Quality Assurance Biotech Jobs in Indiana

A.C. Coy

Sr. Java Developer (Remote)

Indianapolis, IN · Remote

$54.75 - $69.75/hr

This will be a 100% remote Contract-to-Hire position. * Must be a US Citizen. * SELECTED CANDIDATES ... Collaborate with QA, DevOps, UX, and product teams to deliver high-quality solutions. * A degree ...

A.C. Coy

Sr. Java Developer (Remote)

Indianapolis, IN · Remote

$54.75 - $69.75/hr

This will be a 100% remote Contract-to-Hire position. * Must be a US Citizen. * SELECTED CANDIDATES ... Collaborate with QA, DevOps, UX, and product teams to deliver high-quality solutions.

A.C. Coy

Sr. Java Developer (Remote)

Indianapolis, IN · On-site +1

$54.75 - $69.75/hr

This will be a 100% remote Contract-to-Hire position. * Must be a US Citizen. * SELECTED CANDIDATES ... Collaborate with QA, DevOps, UX, and product teams to deliver high-quality solutions.

Millennium Physician Group

$24.20 - $36.30/hr

This is a remote position that can be based anywhere within the United States.** Position ... Actively engage in quality assurance reviews, call audits, and routine feedback to continuously ...

Verawholehealth

$24.20 - $36.30/hr

This is a remote position that can be based anywhere within the United States.** Position ... Actively engage in quality assurance reviews, call audits, and routine feedback to continuously ...

New

CMP.jobs

Sr DevOps Engineer

Indianapolis, IN · Remote

$123K - $158K/yr

Sr. DevOps Engineer 100% Remote Position We have built a cloud-based policy administration platform ... quality assurance, marketing, and project management Requirements ● Professional experience with ...

CMP.jobs

Senior DevOps Engineer

Indianapolis, IN · Remote

$123K - $158K/yr

DevOps Engineer 100% Remote Position We have built a cloud-based policy administration platform ... quality assurance, marketing, and project management Requirements ● Professional experience with ...

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Remote Quality Assurance Biotech information

What is a remote quality assurance biotech?

A Remote Quality Assurance Biotech job involves ensuring that biotechnology products, processes, and systems comply with regulatory standards and company policies, all while working remotely. Professionals in this role review documentation, conduct audits, and collaborate with teams to maintain quality assurance in product development and manufacturing. They help identify potential issues, implement corrective actions, and ensure compliance with industry regulations such as FDA, GMP, or ISO standards. This position requires a strong understanding of biotech processes, attention to detail, and effective communication skills to coordinate quality efforts remotely.

What are the key skills and qualifications needed to thrive in remote quality assurance biotech?

To thrive as a Remote Quality Assurance Biotech professional, you need a strong background in life sciences or biotechnology, experience with quality control processes, and a solid understanding of regulatory standards such as GMP or GLP. Familiarity with digital quality management systems (QMS), data analysis tools, and industry-specific documentation software is often required, along with relevant certifications like ASQ Certified Quality Auditor. Excellent attention to detail, communication skills, and self-motivation are critical for successful remote work and effective cross-functional collaboration. These skills are essential to ensure compliance, maintain product integrity, and facilitate efficient team operations in a remote biotech environment.

What are common challenges faced by remote quality assurance biotech professionals, and how can they be managed?

Remote Quality Assurance Biotech professionals often face challenges such as maintaining clear communication across different teams, managing time zones, and ensuring accurate digital documentation and compliance from a distance. Proactive use of collaboration tools, regular virtual meetings, and strong organizational skills can help address these issues. It is also important to stay current with evolving industry regulations and remote-friendly quality management systems. Building trust with team members and establishing consistent routines can lead to smoother audits and more effective issue resolution, even when working remotely.

What are the most commonly searched types of Quality Assurance Biotech jobs in Indiana?

The most popular types of Quality Assurance Biotech jobs in Indiana are:

What are popular job titles related to Remote Quality Assurance Biotech jobs in Indiana?

For Remote Quality Assurance Biotech jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Remote Quality Assurance Biotech jobs in Indiana look for?

The top searched job categories for Remote Quality Assurance Biotech jobs in Indiana are:

What cities in Indiana are hiring for Remote Quality Assurance Biotech jobs?

Cities in Indiana with the most Remote Quality Assurance Biotech job openings:

Remote Quality Assurance Biotech jobs near you
Infographic showing various Remote Quality Assurance Biotech job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Quality Auditor - Radiopharmaceuticals

SQA Services

Warren, IN • Remote

$4.1K/wk

Full-time

Posted 23 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 Supplier Quality Auditor who has experience working with radiopharmaceuticals. 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
$4,100 - $4,100 one-time
Pay Rate: 
 
$4100 for a 3-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.
 
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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.
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