ZipRecruiter

Log In

1

Gxp Qualification Manager Jobs (NOW HIRING)

Moderna, Inc.

Sr. GxP Product Manager

Cambridge, MA · On-site

$138K - $182K/yr

Here's What You'll Need (Basic Qualifications) The ideal candidate will have strong GxP Business Analyst skills and experience who made a successful transition to a Product Management role. * Minimum ...

Moderna Therapeutics

Sr. GxP Product Manager

Cambridge, MA

$138K - $182K/yr

Here's What You'll Need (Basic Qualifications) The ideal candidate will have strong GxP Business Analyst skills and experience who made a successful transition to a Product Management role. * Minimum ...

ACL Digital

GxP System admininstrator

San Mateo, CA · Hybrid

... work, manage dependencies, and drive operational excellence Qualifications & Experience Bachelor's degree in Computer Science, Information Technology, or related discipline 8+ years of relevant ...

Noblesoft Technologies

GxP Test Lead

Boca Raton, FL · On-site

$45 - $61.50/hr

Experience in testing SAAS/COTS/Bespoke , CRM , Life sciences systems , or lab systems (e.g ... Experience in System Migration and Mobile Testing Qualification: Minimum requirement is a Bachelor ...

next page

Showing results 1-20

All JobsGxp Qualification Manager Jobs

Gxp Qualification Manager information

See salary details

$23K

$61.4K

$102.5K

How much do gxp qualification manager jobs pay per year?

As of Jun 19, 2026, the average yearly pay for gxp qualification manager in the United States is $61,351.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,000.00 per year, depending on experience, location, and employer.

What is the difference between Gxp Qualification Manager vs Gxp Compliance Specialist?

AspectGxp Qualification ManagerGxp Compliance Specialist
CertificationsGxP-related certifications, Quality Management certificationsGxP compliance certifications, Regulatory Affairs certifications
Work EnvironmentRegulatory departments, Quality assurance teams in pharma/biotechRegulatory compliance teams, Quality assurance in pharma/biotech
Industry UsageUsed for managing qualification processes and validation activitiesUsed for ensuring ongoing compliance and adherence to regulations

The Gxp Qualification Manager primarily oversees qualification and validation activities within GxP environments, focusing on ensuring equipment, systems, and processes meet regulatory standards. The Gxp Compliance Specialist concentrates on maintaining ongoing compliance with GxP regulations, audits, and documentation. While both roles require knowledge of GxP regulations and certifications, the Qualification Manager is more involved in qualification planning and execution, whereas the Compliance Specialist emphasizes monitoring and audit readiness.

Infographic showing various Gxp Qualification Manager job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 42% Full Time, 55% Part Time, 1% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $61,351 per year, or $29.5 per hour.

Manager, GxP Quality Systems

Kailera Therapeutics, Inc.

Waltham, MA

Other

Posted 15 days ago

Job description

What You'll Do:

The Manager of GxP Quality Systems will support Quality Management System processes, procedures, systems, training, and tools, ensuring quality and compliance are achieved and maintained across GxP functions. The role will report to the Senior Manager of GxP Quality Systems.

 

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Track and support closure of Quality Events (e.g., Deviations, CAPAs, etc.)
  • Support management of GxP training program, maintenance of GxP training curriculum/matrix, and facilitation and scheduling of GxP trainings
  • Conduct Document Control reviews on controlled quality documents and ensure timely periodic reviews and implementation of document change requests
  • Support establishment, tracking, measurement, and reporting on metrics for the evaluation effectiveness of the Quality Management Systems
  • Support the management of the electronic document management system (Veeva QualityDocs), the electronic learning management system (Veeva Vault Training), and the electronic quality management system (Veeva QMS) as Business Administrator
  • Ensure the systems remain in a validated state, documenting changes via IT Change Controls, and executing scripts with evidence
  • Evaluate opportunities for continuous improvements across the systems
  • Work with stakeholders to ensure appropriate documentation of Service Provider selection, qualification, and evaluation/requalification
  • Support development of metrics related to Service Provider qualifications and Service Provider Quality Events
  • Manage and track Audit Schedule ensuring adherence to Audit Program and timeliness of deliverables

Required Qualifications:

  • Minimum of 6+ years of experience in FDA regulated industry
  • Previous hands-on experience with Veeva Quality Docs, Veeva Training, and Veeva QMS required
  • A strong customer focus and ability to prioritize and adapt to business needs are required
  • Strong business partner with all Functional Areas to ensure efficient collaboration and to drive results
  • Self-motivated, detail oriented, well-organized, and able to demonstrate success with managing multiple projects simultaneously and other priorities
  • Ability to resolve day-to-day issues efficiently while maintaining compliance with applicable industry standards
  • Clear, concise writing skills and good verbal communication and presentation skills

Education:

  • Bachelor's degree in Life Sciences or a related field

Apply