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Part Time Fda Compliance Jobs (NOW HIRING)

Alcanza

Part-time Pharm Tech

Decatur, GA

$17 - $20.75/hr

The Investigational Product Coordinator is responsible for preparing and dispensing study drug, providing drug-related information to subjects and staff in compliance with GCP, ICH, HIPAA, FDA, USP ...

IHRC, Inc.

Senior Health Physicist

Silver Spring, MD · On-site

Job Type Part-time Description IHRC Inc. is seeking a part-time (estimated to be up to 10 hours ... Provide technical guidance and support for radiation safety and health physics programs at FDA ...

Meijer, Inc.

PART TIME Asset Protection Officer

Newport, MI · On-site

$13.75 - $15.50/hr

This position needs experience with OSHA, EPA, FDA regulations, and enforcement of regulatory/environmental compliance. What You'll be Doing: * Conduct hazardous emergency evacuation drills including ...

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Part Time Fda Compliance information

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$27K

$49.5K

$84K

How much do part time fda compliance jobs pay per year?

As of Sep 2, 2026, the average yearly pay for part time fda compliance in the United States is $49,486.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,000.00 and $57,000.00 per year, depending on experience, location, and employer.

What is a part time FDA compliance job?

Part-time FDA compliance jobs involve working on a flexible or reduced-hour schedule to help organizations ensure their products and processes meet the standards set by the U.S. Food and Drug Administration (FDA). These professionals may review documentation, assist with audits, monitor regulatory changes, and support teams in maintaining compliance with FDA guidelines. Part-time roles are common in industries like pharmaceuticals, medical devices, food, and cosmetics, offering flexibility for those who may be balancing other commitments. The work requires a strong understanding of FDA regulations and attention to detail to help organizations avoid penalties and ensure public safety.

What skills and qualifications are needed to thrive as a part time FDA compliance specialist?

To thrive as a Part Time FDA Compliance Specialist, you need a solid understanding of FDA regulations, quality assurance practices, and industry standards, often supported by a degree in life sciences or a related field. Familiarity with compliance management systems, documentation software, and relevant certifications like RAC (Regulatory Affairs Certification) is commonly required. Attention to detail, strong organizational skills, and effective communication are vital soft skills for ensuring regulatory adherence and collaborating with cross-functional teams. These qualifications and skills are essential for maintaining product safety, minimizing regulatory risks, and supporting successful audits.

What are the primary challenges faced by part time FDA compliance professionals, and how can they manage these responsibilities?

Part-time FDA compliance professionals often face the challenge of staying current with frequently changing regulations while managing their time efficiently. Balancing multiple tasks, such as maintaining documentation, conducting audits, and reporting noncompliance, requires strong organizational skills and proactive communication with full-time team members. Successful professionals leverage digital tools, prioritize tasks based on regulatory deadlines, and maintain clear documentation to ensure nothing falls through the cracks. Collaborating closely with other departments, such as quality assurance and manufacturing, helps in staying aligned with regulatory expectations and team goals.

What is the difference between Part Time Fda Compliance vs Part Time Quality Assurance Specialist?

AspectPart Time Fda CompliancePart Time Quality Assurance Specialist
Required CertificationsFDA regulations, compliance trainingISO standards, quality management systems
Work EnvironmentRegulatory agencies, manufacturing facilitiesManufacturing plants, laboratories
Employer & Industry UsagePharmaceutical, food, medical device companiesManufacturing, biotech, pharmaceutical sectors

Part Time Fda Compliance focuses on ensuring products meet FDA regulations, while Part Time Quality Assurance Specialists concentrate on maintaining quality standards. Both roles require knowledge of industry regulations but differ in scope and certification emphasis. They are often found in similar industries and work environments, making them common points of comparison for professionals seeking compliance or quality roles.

More about Part Time Fda Compliance jobs

What are the most commonly searched types of Fda Compliance jobs?

The most popular types of Fda Compliance jobs are:

What states have the most Part Time Fda Compliance jobs?

States with the most job openings for Part Time Fda Compliance jobs include:

What job categories do people searching Part Time Fda Compliance jobs look for?

The top searched job categories for Part Time Fda Compliance jobs are:

Part Time Fda Compliance jobs near you
Infographic showing various Part Time Fda Compliance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $49,486 per year, or $23.8 per hour.

Document Specialist (Part-TIme)

Ursitti Enterprises LLC

Portage, IN • On-site

$19 - $20/hr

Part-time

Re-posted 22 days ago

Job description

Leading Pharmaceutical Manufacturer Requires a Part-Time 1st Shift Document Specialist at their Portage Facility! If you meet the qualifications below, APPLY NOW!

$20.00/Hour


Job Description:

We seek a meticulous and organized Document Specialist to join our client's team in Portage. As a Document Specialist, you will be crucial in managing and maintaining various documents critical to their operations, including regulatory submissions, standard operating procedures (SOPs), clinical trial documents, and other essential records.

Responsibilities:

  • Document Management: Ensure the accurate and timely creation, revision, and maintenance of documents, adhering to established guidelines and regulatory requirements.
  • Quality Control: Perform thorough quality checks on documents to ensure accuracy, consistency, and compliance with internal standards and regulatory guidelines.
  • Document Review: Review documents for completeness, correctness, and clarity, collaborating with relevant stakeholders to address discrepancies or issues.
  • Version Control: Manage document versions effectively, maintaining a clear and organized version history to facilitate tracking and retrieval.
  • Documentation Support: Support various departments by assisting in preparing, formatting, and distributing documents as needed.
  • Training and Compliance: Assist in training employees on document management processes and procedures to ensure compliance with company policies and regulatory standards.
  • Continuous Improvement: Identify opportunities for process improvements and efficiency enhancements within the document management system.

Qualifications:

  • Bachelor's degree or equivalent experience in a relevant field of life sciences, business administration, or related discipline).
  • Previous experience in document management, preferably within the pharmaceutical or healthcare industry.
  • Strong attention to detail and excellent organizational skills, with the ability to effectively manage multiple tasks and priorities.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and document management software.
  • Familiarity with regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GCP, GMP) preferred.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.