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Part Time Gmp Auditor Jobs (NOW HIRING)

GMP/GLPproficiency. * IVD,MDSAP, ISO 13485 or similar compliance experience * Proficiency in MS ... Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your ...

Part Time Gmp Auditor information

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$10

$19

$46

How much do part time gmp auditor jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for part time gmp auditor in the United States is $19.21, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Part Time GMP Auditor, and why are they important?

To thrive as a Part Time GMP Auditor, you need in-depth knowledge of Good Manufacturing Practices, regulatory compliance, and quality management systems, typically supported by a background in life sciences or a related field. Familiarity with audit management software, documentation systems, and relevant certification such as ISO or GMP auditor credentials is highly valued. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for conducting thorough audits and delivering clear findings. These skills ensure that organizations maintain compliance, minimize risks, and uphold product quality and safety standards.

What is the difference between Part Time Gmp Auditor vs Part Time Gmp Inspector?

AspectPart Time Gmp AuditorPart Time Gmp Inspector
CertificationsGMP Auditor Certification, relevant quality assurance credentialsGMP Inspector Certification, quality control training
Work EnvironmentAuditing manufacturing facilities, documentation reviewInspecting production lines, on-site compliance checks
Employer & Industry UsagePharmaceutical, biotech, and supplement companiesRegulatory agencies, manufacturing plants

While both roles focus on GMP compliance, Part Time Gmp Auditors primarily review documentation and processes through audits, whereas Part Time Gmp Inspectors conduct on-site inspections to verify adherence to GMP standards. The roles often overlap but differ in their approach and scope within the industry.

What are some common challenges faced by part-time GMP Auditors, and how can they effectively manage their workload?

Part-time GMP Auditors often face the challenge of balancing audit responsibilities with limited hours, which can make time management and prioritization crucial. They need to efficiently review documentation, conduct site visits, and prepare reports within a condensed schedule. To manage this, it's important to maintain clear communication with the quality assurance team and clients, set realistic goals for each audit, and stay updated on current GMP regulations. Leveraging digital tools and checklists can also help streamline the audit process and ensure thoroughness despite time constraints.

What are part time GMP auditors?

Part time GMP (Good Manufacturing Practice) auditors are professionals who assess manufacturing facilities and processes to ensure they comply with regulatory standards, but do so on a part-time or contract basis. Their main responsibilities include reviewing documentation, inspecting facilities, and identifying areas for improvement to maintain product quality and safety. Part time auditors often work for multiple organizations or as independent consultants, offering flexibility for both the auditor and employer while maintaining high compliance standards.
More about Part Time Gmp Auditor jobs
What are the most commonly searched types of Gmp Auditor jobs? The most popular types of Gmp Auditor jobs are:
Infographic showing various Part Time Gmp Auditor job openings in the United States as of May 2026, with employment types broken down into 59% Full Time, 40% Part Time, and 1% Contract. Highlights an 87% Physical, 6% Hybrid, and 7% Remote job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Quality Assurance Coordinator

Revvity

San Diego, CA • On-site

$26.20 - $34/hr

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Revvity rating

9.5

Company rating: 9.5 out of 10

Based on 8 frontline employees who took The Breakroom Quiz


Job description

BioLegend | About Us

At BioLegend, we are committed to providing researchers with the most comprehensive and cutting-edge high-quality reagents for life science research. Being part of Revvity, a global provider of health science solutions, technologies, expertise and services for life sciences and diagnostics, allows us to extend the mission of enabling our customers to do legendary discovery. Join us and make a difference!

BioLegends Quality Assurance Coordinator is responsible for supporting applicable Quality Assurance processes which may include non-conformances, complaint management, field corrective actions, risk management, design control, CAPA, document and change control, training, batch release, auditing and validation under direct supervision. This role requires strong attention to detail, the ability to communicate and a willingness to adapt to changing business needs.

Essential Functions

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Acts in a support capacity for critical QMS processes such as, non-conformances, complaint management, field corrective actions, risk management, design control, CAPA, document and change control, training, batch release, auditing, supplierManagementand validation.

  • Reviews quality records for all related areas of responsibility.

  • Demonstrates the ability to work with limited direction and can prioritize projects independently

  • Responsible for personal daily task management, trainingplansand performance management.

  • Assistwithgenerating, reviews andmaintainsQMS documents.

  • Assistwithmonitoring and trending QMS elements and providing metrics data for monthly reports, qualityobjectivesand key performance indicators (KPIs).

  • Assistswith data preparation for Quality Management Reviews.

  • Provides administrative support for external audits (regulatory or customer) and Internal Audits.

  • Participates in the use of theeQMSsystem and expanded applications asappropriate.

  • This position will interact with key internal stakeholders in Manufacturing, Facilities, IT, R&D, CustomerSupportand Supply Chain.

  • Assistwithmonthly andmanagementreviewdata and metrics for areas of responsibility.

  • Other projects orresponsibilities asmay berequired.

MinimumQualificationsEducation and Experience

  • Bachelor's degree in a scientific discipline or equivalent work experience.

Preferred Qualifications Education and Experience

  • 1-yearwork experience in Quality Assurance.

  • 0-6+ months of experience withGMPor similar regulatedproducts. GMP/GLPproficiency.

  • IVD,MDSAP, ISO 13485 or similar compliance experience

  • Proficiency in MS Word, Excel,PowerPoint, Adobe Acrobat (PDF)

Work Environment& Physical Demands

Office

While performing the duties of this job, the employeeregularly worksin an office setting.Occasional exposure to a laboratoryand warehouseenvironment.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employeeis regularly required touse hands and fingers to handle, feel, oroperateobjects,toolsor controls, and reach with hands and arms. The employee isfrequentlyrequired to stand,talkand hear.

The base salary range for this full-time position is $26.20 - $34.00/hour. This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not takeinto account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.


What do we offer?

We provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits:

  • Medical, Dental, and Vision Insurance Options
  • Life and Disability Insurance
  • Paid Time-Off
  • Parental Benefits
  • Compassionate Care Leave
  • 401k with Company Match
  • Employee Stock Purchase Plan

Learn more about Revvitys benefits by visiting our Bswift page. Log-In instructions are provided towards the bottom of the Bswift page.

For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information.

Apply Now

About Revvity

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

2023