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Live In Glp Qa Jobs (NOW HIRING)

Celldex Therapeutics

GLP QA Specialist II

Fall River, MA · On-site

$76K - $99K/yr

Manage GLP QA periodic reports * Assist in GLP QA systems execution supporting GLP testing * Create, trend, and report GLP QA Quality Systems information * Perform internal GLP audits Qualifications

Celldex Therapeutics

GLP QA Specialist II

Fall River, MA · On-site

$76K - $99K/yr

Manage GLP QA periodic reports * Assist in GLP QA systems execution supporting GLP testing * Create, trend, and report GLP QA Quality Systems information * Perform internal GLP audits * Bachelor ...

Labcorp

Quality Auditor - GLP/GCP

Indianapolis, IN · On-site

The Quality Auditor plays a pivotal role as part of our Quality Assurance team in ensuring that ... GCP/GLP, ISO 15189, ISO 13485 and CAP. Job Responsibilities: * Conduct work as identified on the ...

Labcorp

Quality Auditor - GLP/GCP

Indianapolis, IN

The Quality Auditor plays a pivotal role as part of our Quality Assurance team in ensuring that ... GCP/GLP, ISO 15189, ISO 13485 and CAP. Job Responsibilities: * Conduct work as identified on the ...

Agenus, Inc.

Director, Quality Assurance

Lexington, MA · On-site

In the role you will: * Support batch record and SOP/Method development, review quality systems and ... Lead the development, implementation, and continuous improvement of our GMP, GCP, and GLP quality ...

CSS, Inc

Quality Assurance (QA) Auditor

Chapel Hill, NC · On-site

Committed to delivering high-quality, GLP-compliant QA products that support NIEHS/NTP's mission in public health. Work Authorization, Government Agency Clearance, and Security Clearance Requirements

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How much do live in glp qa jobs pay per year?

As of Aug 30, 2026, the average yearly pay for live in glp qa in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

What is the difference between Live In Glp Qa vs Live In Glp Auditor?

AspectLive In Glp QaLive In Glp Auditor
CertificationsGMP, GLP knowledge, QA certificationsGMP, GLP, QA certifications
Work EnvironmentPharmaceutical or biotech labs, manufacturing facilitiesPharmaceutical or biotech labs, manufacturing facilities
Employer & IndustryPharma companies, contract research organizationsPharma companies, contract research organizations
Primary FocusEnsuring GLP compliance in QA processesAuditing GLP compliance and documentation

Both Live In Glp Qa and Live In Glp Auditor roles involve ensuring GLP compliance within pharmaceutical environments. The main difference is that Live In Glp Qa focuses on quality assurance activities, while Live In Glp Auditor emphasizes conducting audits and assessments. Both positions require similar certifications and work in comparable environments, but their core responsibilities differ slightly.

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GLP QA Specialist II

Fall River, MA • On-site

Celldex Therapeutics
Biotechnology Research and Development • 201 - 500 employees
Learn more about Celldex Therapeuticsexternal

$76K - $99K/yr

Other

Medical, Retirement, PTO

Re-posted 11 days ago

Job description

Overview
This role is responsible for maintaining quality systems, tracking and reporting QA metrics, managing laboratory documentation processes, and ensuring adherence to FDA GLP requirements while partnering with cross-functional teams to drive continuous improvement and quality excellence. The ideal candidate is detail-oriented, highly organized, and capable of working independently and collaboratively to support the integrity, accuracy, and compliance of quality operations across the organization.
Responsibilities
  • Maintain GLP document control system including preparing, updating, formatting, distributing, issuing, and tracking GXP documents
  • Manage, distribution, and reconciliation of laboratory notebooks
  • Manage GLP QA periodic reports
  • Assist in GLP QA systems execution supporting GLP testing
  • Create, trend, and report GLP QA Quality Systems information
  • Perform internal GLP audits

Qualifications
  • Bachelor Science (BS)/Bachelor Arts (BA) degree in Life Sciences preferable.
  • 1-3 years QA experience in Biotech/Pharma industry.
  • Strong working knowledge of EDMS (electronic document management system)
  • Strong working knowledge of cGMP/GLP.
  • Strong working knowledge of MS Word, Excel and related databases
  • The ability to work independently and as part of a team
  • Excellent communication skills.

Compensation
The expected base salary range for this position is $76,374 to $99,189
We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach

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