ZipRecruiter

Log In

1

Live In Glp Qa Jobs (NOW HIRING)

Frontage Laboratories

QA Manager

Exton, PA · On-site

Experience * 5+ years of QA, QC, GLP, or regulated laboratory experience in CRO, pharmaceutical, biotechnology, or related industries. * Experience supporting GLP studies and quality systems ...

SNAP Diagnostics

RA QA SPECIALIST

Vernon Hills, IL · On-site

$65K - $85K/yr

Must live in the local area. Key Responsibilities * Implement and maintain quality standards across ... Familiarity with GMP, GLP, GCP, FDA, or ISO standards * Strong problem-solving and risk assessment ...

SystImmune, Inc

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

Maintain and improve the Quality Management System (QMS) in compliance with Bioanalytical Lab QA (GLP/FDA) and CLIA/CAP across Clinical Pathology and Bioanalytical labs * Develop, review, and approve ...

Neuralink

Quality Assurance Specialist

Austin, TX · On-site

$26.92 - $44.71/hr

Conduct audits of Good Laboratory Practice (GLP) activities within Neuralink, and when needed ... Bachelor of Science degree, preferably in a science, engineering, or quality-related discipline

Bureau Veritas

Quality Assurance Lead

Knoxville, TN · On-site

$75K - $90K/yr

Participate in cross-departmental corrective activities based on trends * Support quality event ... Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership * Train and develop ...

Neuralink

Quality Assurance Specialist

Austin, TX · On-site

$26.92 - $44.71/hr

Conduct audits of Good Laboratory Practice (GLP) activities within Neuralink, and when needed ... Bachelor of Science degree, preferably in a science, engineering, or quality-related discipline

Integrated Resources INC

QA Manager

East Windsor, NJ · On-site

Ensure all GMP, GLP, GCP operations are in compliance , Establish training and audit programs, as ... Be responsible for release or rejection of GMP materials and utilize QA staff to manage the ...

Actalent

QA Manager

Happy Valley, OR

Coordinate, implement, and maintain the laboratory's Quality Management System in collaboration ... Serve as archivist for Good Laboratory Practice (GLP) study-specific records, ensuring proper ...

SAB

Quality Assurance Manager

Sioux Falls, SD · On-site

This role provides quality oversight for GxP operations, including cGMP, GCP/GCLP, GLP, Good ... Bachelor's degree in biology, microbiology, chemistry, biochemistry, pharmaceutical sciences, or a ...

Elanco

Senior Associate-Quality Assurance

Fort Dodge, IA · On-site

Quality Assurance Associate - R&D Quality Assurance As a Quality Assurance Associate - R&D Quality ... In this role, you will help advance GLP compliance, quality systems oversight, and audit readiness ...

Bunge

Quality Assurance Tech Oils

Sandston, VA · On-site

$17 - $24/hr

GLP, Laboratory and Food Safety. GMP, Allergens, Moisture and Salt Analysis, and Oil Testing. PCQI ... Bunge offers a strong compensation and benefits package and most importantly, in all we do we live ...

TalentBurst, Inc.

NC

This position will report to the Quality Assurance Manager (GCP/GLP). Responsibilities ... Perform in-process inspections of nonclinical study phases and assay methods. * Review study events ...

Clingroup

Junior Quality Assurance Specialist

Waverly, NY · On-site

$68K - $72K/yr

... in invitro, pre-clinical, and clinical trials to evaluate the safety, metabolism, and efficacy of ... Support compliance with GLP, GCP, international guidelines, regulatory requirements, applicable ...

previous pagenext page

Showing results 21-40

All JobsLive In Glp Qa Jobs

Live In Glp Qa information

See salary details

$38K

$118.1K

$179K

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

As of Aug 8, 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.

What cities are hiring for Live In Glp Qa jobs? Cities with the most Live In Glp Qa job openings:
What are the most commonly searched types of Glp Qa jobs? The most popular types of Glp Qa jobs are:
Live In Glp Qa jobs near you

Senior Director / Director, Quality Assurance

Attovia Therapeutics

San Carlos, CA • Remote

Full-time

Posted 23 days ago

Job description

Attovia Therapeutics, Inc., is seeking a Sr. Director/Director of Quality Assurance to lead our quality function and oversee the performance of our external CDMO/CRO partners, who execute the majority of our GMP manufacturing, testing, and clinical activities. Reporting directly to the Quality Officer, this role is responsible for vendor quality management: qualifying and auditing CDMOs/CROs, negotiating and maintaining Quality Agreements, performing final quality review for batch release and lot disposition, and ensuring the company's internal Quality Management System (QMS) ties together all outsourced activity into a single, inspection-ready compliance picture. This role partners closely with CMC, Clinical Operations, Nonclinical/Preclinical Development, and Regulatory Affairs teams to ensure that our outsourced partners consistently deliver compliant, high-quality work that meets regulatory expectations and protects patient safety.
Key Responsibilities

Quality Strategy & Leadership

  • Working closely with the Quality Officer, CMC and clinical leadership, help set strategic direction and priorities for the quality function.
  • Represent Quality in regulatory strategy discussions, partnership/licensing diligence, and CDMO/CRO selection decisions.

CDMO Quality Oversight

  • Own quality oversight of CDMO activities, ensuring external partners operate in compliance with FDA, EMA, ICH, other applicable global regulations, and quality agreements.
  • In partnership with the CMC team, review and approve CDMO executed batch records, protocols, and quality documentation, confirming that all GMP requirements are met and that the quality record supporting each batch release decision is complete and traceable.
  • Drive proactive, risk-based oversight of CDMO quality systems, including deviations, investigations, CAPAs, change controls.
  • Support technology transfer and process validation activities performed at CDMO sites, including protocol/report review and approval to ensure manufacturing readiness for commercialization.

Clinical & Nonclinical CRO Oversight

  • Provide GCP/GLP quality oversight of CROs supporting clinical trials and nonclinical/toxicology studies to ensure all activities are conducted in strict compliance with FDA, EMA, ICH, other applicable global regulations, and quality agreements.
  • Working with Clinical QA consultant, review clinical quality documentation, monitor CRO audit findings, and track resolution of quality issues affecting trial data integrity.
  • Partner with Clinical Operations and Clinical QA consultants to ensure vendor oversight plans and risk-based monitoring approaches remain aligned with GCP requirements.
  • Provide support for clinical deviations and CAPA management. Identify and assess compliance risk and develop and implement risk mitigation measures.

Vendor Qualification, Audits & Quality Agreements

  • Drive vendor audits and qualification to ensure external partners maintain compliant, inspection-ready systems
  • Draft, negotiate, and maintain Quality Agreements defining roles, responsibilities, and quality standards between the company and each vendor.
  • Maintain the approved vendor list and associated risk assessments.

Quality Management System (QMS)

  • Working across internal functions and with external clinical/nonclinical QA consultants, drive the development of the internal QMS, including SOPs governing vendor oversight, deviations, CAPA, change control, document control, clinical operations, data management, pharmacovigilance, biostatistics, and training, and continuously improve it to support scaling clinical pipelines.
  • Maintain document control systems for controlled documents, quality agreements, and vendor quality records.
  • Training & Quality Culture
  • Develop and deliver GxP yearly training for internal staff, and champion a strong, risk-based quality culture across a small, cross-functional organization.
Basic Qualifications
  • Bachelor's or Master's degree in Life Sciences, Chemistry, Engineering, or a related technical discipline.
  • Experience in biologics, cell & gene therapy, or sterile injectable products.
  • 12+ years of Quality Assurance experience in the biotech/pharmaceutical industry, with direct experience managing outsourced GMP manufacturing and/or testing relationships (CDMO experience required).
  • Strong working knowledge of global GMP requirements including FDA, EMA, ICH guidelines, and applicable GCP/GLP regulations.
  • Demonstrated experience auditing contract manufacturers, testing labs, depot, or CROs, and negotiating Quality Agreements.
  • Experience reviewing batch records, CoAs, deviations, and change controls generated by external parties.
Preferred Qualifications
  • Strong technical writing, investigative, and risk-assessment skills.
  • Ability to work independently and manage multiple vendor relationships with minimal direct supervision
  • Prior experience as the sole or lead quality function at a small or virtual biotech company.
  • Familiarity with electronic QMS platforms (e.g., Veeva QMS, MasterControl, TrackWise).
  • Experience supporting a pre-approval inspection (PAI) or BLA/NDA filing.
About Attovia

Attovia is a clinical-stage biopharmaceutical company developing next-generation biotherapeutics for immune-mediated diseases with high unmet need.  Our product candidates are internally discovered using our proprietary ATTOBODY platform, an evolution-driven, high-throughput biologics platform that enables the rapid discovery and creation of diverse biparatopic complex biologics.  Our pipeline spans chronic pruritic diseases, inflammatory skin diseases, inflammatory bowel disease, and other immune-mediated conditions.

Our culture is centered around five core pillars: 
     Integrity 
     Learning & Growth 
     Drive for Excellence 
     Innovation 
     Teamwork & Collaboration 
We take pride in fostering a strong team and dynamic work environment, and we are seeking individuals who align with our values and contribute to a positive and impactful workplace.  
Attovia is located in San Carlos, CA.
Attovia is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, or veteran or disability status.  
Learn more about Attovia: www.attovia.com

$210,000 - $280,000 a year
Leveling and salary is commensurate with experience.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job

Apply