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Weekend Gmp Auditor Jobs (NOW HIRING)

TekWissen LLC

Laboratory Technician 1

Walpole, MA · On-site

$43/hr

This role will provide weekend coverage, Tuesday - Saturday or Sunday - Thursday with training ... Auditing and GMP/GDP verification of batch records and product release responsibilities Details of ...

The Pictsweet Company

Director, Food Safety

Bells, TN · On-site

... GMP, SOP's, and Internal Auditing. * Assure that The Pictsweet Company maintains its systems and ... Be willing to work flexible hours, including weekends and holiday, travel to company facilities ...

The Pictsweet Company

Director, Food Safety

Bells, TN · On-site

... GMP, SOP's, and Internal Auditing. * Assure that The Pictsweet Company maintains its systems and ... Be willing to work flexible hours, including weekends and holiday, travel to company facilities ...

The Pictsweet Company

Director, Food Safety

Bells, TN · On-site

... GMP, SOP's, and Internal Auditing. * Assure that The Pictsweet Company maintains its systems and ... Be willing to work flexible hours, including weekends and holiday, travel to company facilities ...

Pictsweet Company

Director, Food Safety

Bells, TN · On-site

... GMP, SOP's, and Internal Auditing. * Assure that The Pictsweet Company maintains its systems and ... Be willing to work flexible hours, including weekends and holiday, travel to company facilities ...

Fairway Staffing Solutions

QA/QC Tech

Fullerton, CA · On-site

$21 - $23/hr

Must be available for overtime and weekend workMust follow all GMP policies and proceduresQuality ... This person reports directly to the QA Manager, and liaise with health auditors, customer, third ...

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Weekend Gmp Auditor information

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How much do weekend gmp auditor jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for weekend gmp auditor in the United States is $18.94, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $19.95 per hour, depending on experience, location, and employer.

What is a weekend GMP auditor?

Weekend GMP Auditors are professionals who conduct audits of manufacturing facilities, typically in the pharmaceutical, biotechnology, or food industries, to ensure compliance with Good Manufacturing Practice (GMP) regulations. These auditors work specifically on weekends, allowing companies to minimize disruption to regular operations. Their responsibilities include reviewing documentation, inspecting processes, and identifying areas for improvement to ensure products are consistently produced and controlled according to quality standards. Weekend GMP Auditors play a vital role in maintaining regulatory compliance and product safety. They often possess expertise in quality assurance, regulatory requirements, and industry best practices.

What skills and qualifications are needed to be a weekend GMP auditor?

To thrive as a Weekend GMP Auditor, you need a solid understanding of Good Manufacturing Practices, quality assurance principles, and often a relevant science or engineering degree. Familiarity with industry regulations (such as FDA or EU GMP), audit management software, and certifications like Certified Quality Auditor (CQA) are typically required. Strong attention to detail, analytical thinking, and effective communication skills help auditors identify issues and clearly report findings. These competencies ensure compliance, product safety, and continuous improvement within regulated manufacturing environments.

What unique challenges might a weekend GMP auditor face compared to weekday auditors?

Weekend GMP Auditors often encounter unique challenges such as limited on-site support staff and restricted access to certain production areas or documentation, which can require proactive planning and communication. Additionally, coordinating interviews or walkthroughs with key personnel may need to be scheduled in advance due to reduced weekend staffing. Despite these challenges, weekend auditors play a critical role in ensuring continuous compliance and often develop strong problem-solving skills by working independently. The role also offers exposure to a variety of shifts and processes, which can be valuable for career advancement in quality assurance or regulatory roles.

What is the difference between Weekend Gmp Auditor vs Gmp Compliance Specialist?

AspectWeekend Gmp AuditorGmp Compliance Specialist
CertificationsGMP Auditor Certification, relevant industry trainingGMP Certification, compliance training
Work EnvironmentPart-time, on-site audits during weekendsFull-time, office and on-site compliance roles
Employer & Industry UsagePharmaceutical, biotech companies, contract auditing firmsPharmaceutical companies, regulatory agencies, consulting firms

The Weekend Gmp Auditor primarily conducts audits during weekends, focusing on quality assurance and compliance checks. In contrast, a Gmp Compliance Specialist typically works full-time to develop, implement, and monitor GMP policies. Both roles require GMP certifications and are integral to maintaining industry standards, but they differ mainly in work hours and scope of responsibilities.

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Weekend Gmp Auditor jobs near you
Infographic showing various Weekend Gmp Auditor job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 65% Full Time, 30% Part Time, 3% Contract, and 1% Nights. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $39,400 per year, or $18.9 per hour.

Laboratory Technician 1

Walpole, MA • On-site

TekWissen LLC
Recruiting and Staffing Services • 501 - 1,000 employees
Learn more about TekWissen LLCexternal

$43/hr

Contractor

Re-posted 23 days ago

Job description

Overview:           
     
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The below client is with one of our client which is a leading global medical technology company. It offers a wide range of diagnostic imaging and laboratory diagnostics, as well as advanced therapies and digital health services. Its solutions span from prevention and early detection to diagnosis, treatment, and follow-up care, empowering healthcare providers worldwide.    
      
Job Title: Laboratory Technician 1
Location: Walpole, MA, 02032   
Duration: 12 Months    
Job Type: Contract    
Work Type: Onsite   
Shift: 8am - 4:3pm   
   
Job Description:   
 
The primary resposnbility of this role is chromatography manufacturing. The scope of this role includes manufacture of production batches for the Concentrates work center. The scope of this role may include manufacture of production batches for the Purification work center. The scope of this role includes auditing of chromatography batch records. This role will provide weekend coverage, Tuesday – Saturday or Sunday - Thursday with training occurring on Monday – Friday. Candidate must demonstrate the ability to understand formulation processes, work with processes and equipment, detailed written documentation of work, ability to work well with others, and compliance.
This position includes the handling of all types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials.
As a Biochemist 1, will be responsible for:
  • Manufacturing of Concentrates, Purified Antibodies, and Purified Conjugates via liquid chromatography
  • Auditing and GMP/GDP verification of batch records and product release responsibilities
Details of job tasks include:
  • Following established manufacturing protocols to conjugate and/or isolate proteins for use in immunological assays.
  • Buffer and chromatography column preparation
  • Maintaining a legible and accurate batch record according to proper GMP
  • Making decisions and executing critical steps in the manufacturing process
  • Maintaining an FDA/DEA compliant laboratory
  • Providing Quality Notification Support
  • Executing temporary manufacturing deviations and pilot products
  • Completion of all necessary training activities
Required Knowledge/Skills, Education, and Experience
  • Bachelor’s Degree required. (Biology, Chemistry, Engineering, or other applicable Science Degree)
  • 3-5 years chromatography work experience.
  • Proficiency with basic lab equipment (pipettes, balances, centrifuges)
  • Proficiency in Microsoft Office Programs
  • Strong communication and organizational skills
  • Strong mathematical and critical thinking skills
  • Must have legible handwriting
  • Must be able to safely lift 50lbs
  • Must pass a Drug Enforcement Agency (DEA) background check.
Preferred Knowledge/Skills, Education, and Experience
  • Experience with AKTAs
  • A background in manufacturing processes
  • Familiarity with GMP/GDP guidelines
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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