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 ...
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 ...
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 ...
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 ...
Quality Assurance Manager
Bothell, WA · Remote
About this role: The Quality Assurance Manager plays a critical role in supporting and ... in development. * Experience performing GCP, GCLP, GLP, and GMP audits a plus. * Ability to ...
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Quality Assurance Manager
Bothell, WA · Remote
About this role: The Quality Assurance Manager plays a critical role in supporting and ... in development. * Experience performing GCP, GCLP, GLP, and GMP audits a plus. * Ability to ...
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 ...
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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 ...
Quality Assurance Manager
Portland, OR · On-site
Registered Quality Assurance Professional for GLP regulations (RQAP-GLP) * Laboratory analytical experience TRAINING REQUIREMENTS OJT in understanding company operating systems, including the ...
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Quality Assurance Manager
Portland, OR · On-site
Registered Quality Assurance Professional for GLP regulations (RQAP-GLP) * Laboratory analytical experience TRAINING REQUIREMENTS OJT in understanding company operating systems, including the ...
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 ...
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 ...
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 ...
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 ...
... in human centered design and product development, preclinical and clinical research, regulatory ... Perform contemporaneous and detailed QC reviews of GLP and non-GLP study records, raw data forms ...
... in human centered design and product development, preclinical and clinical research, regulatory ... Perform contemporaneous and detailed QC reviews of GLP and non-GLP study records, raw data forms ...
... GCP, GLP, GVP, and CDx strategies and participate in the further development of a high functioning Quality organization. Essential Duties and Responsibilities: * Ensure strategic and tactical ...
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... GCP, GLP, GVP, and CDx strategies and participate in the further development of a high functioning Quality organization. Essential Duties and Responsibilities: * Ensure strategic and tactical ...
Your Role: R&D Quality Assurance Auditor As an R&D Quality Assurance Auditor, you will be part of ... RQAP-GLP certification. * Experience supporting or participating in regulatory authority ...
Your Role: R&D Quality Assurance Auditor As an R&D Quality Assurance Auditor, you will be part of ... RQAP-GLP certification. * Experience supporting or participating in regulatory authority ...
Minimum 7 years QA GMP experience in biotech/pharmaceutical environment required. GCP and GLP experience a plus. * Demonstrated knowledge and understanding of quality compliance principles with ...
Minimum 7 years QA GMP experience in biotech/pharmaceutical environment required. GCP and GLP experience a plus. * Demonstrated knowledge and understanding of quality compliance principles with ...
... GLP, GVP, and CDx strategies and participate in the further development of a high functioning ... Represent clinical QA on project and study teams, perform technical review of Clinical Study ...
... GLP, GVP, and CDx strategies and participate in the further development of a high functioning ... Represent clinical QA on project and study teams, perform technical review of Clinical Study ...
Sr/Exec Director, Quality Assurance GCP
San Diego, CA · On-site +1
... GCP, GLP, GVP, and CDx strategies and participate in the further development of a high functioning Quality organization. Essential Duties and Responsibilities: * Ensure strategic and tactical ...
Sr/Exec Director, Quality Assurance GCP
San Diego, CA · On-site +1
... GCP, GLP, GVP, and CDx strategies and participate in the further development of a high functioning Quality organization. Essential Duties and Responsibilities: * Ensure strategic and tactical ...
Quality Assurance Manager
Bothell, WA · Remote
Provide QA review and approval for Master Batch Records, protocols, reports, and SOPs, ensuring ... in development. * Experience performing GCP, GCLP, GLP,and GMPauditsa plus. * Ability ...
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Quality Assurance Manager
Bothell, WA · Remote
Provide QA review and approval for Master Batch Records, protocols, reports, and SOPs, ensuring ... in development. * Experience performing GCP, GCLP, GLP,and GMPauditsa plus. * Ability ...
Live In Caregiver
Pipersville, PA · On-site
$190 - $200/day
Training & development Live-In Caregivers needed throughout Bucks and Montgomery County Join our ... Our caregivers are held to the highest standards through screening, training and quality assurance.
Live In Caregiver
Pipersville, PA · On-site
$190 - $200/day
Training & development Live-In Caregivers needed throughout Bucks and Montgomery County Join our ... Our caregivers are held to the highest standards through screening, training and quality assurance.
... GCP, GLP, GVP, and CDx strategies and participate in the further development of a high functioning Quality organization. Essential Duties and Responsibilities: * Ensure strategic and tactical ...
Quick apply
... GCP, GLP, GVP, and CDx strategies and participate in the further development of a high functioning Quality organization. Essential Duties and Responsibilities: * Ensure strategic and tactical ...
Serving as the GCP QA lead for late-stage clinical programs, this individual is accountable for GCP, GLP, and Pharmacovigilance/Safety oversight across multiple RevMed studies and represents QA in ...
Serving as the GCP QA lead for late-stage clinical programs, this individual is accountable for GCP, GLP, and Pharmacovigilance/Safety oversight across multiple RevMed studies and represents QA in ...
Director of Quality Assurance, Clinical
Berkeley, CA · On-site +1
Responsible for leading in the development, implementation and maintenance of QA systems and activities supporting quality oversight towards GCP, GLP, and PV operations. The incumbent will assist in ...
Director of Quality Assurance, Clinical
Berkeley, CA · On-site +1
Responsible for leading in the development, implementation and maintenance of QA systems and activities supporting quality oversight towards GCP, GLP, and PV operations. The incumbent will assist in ...
Quality Assurance Lead
Morrow, GA · On-site
... in accordance with training and display an acceptable level of competency with all Quality ... CCP's, GLP's, Hold/Release, and Environmental Sampling. The individual must also request additional ...
Quality Assurance Lead
Morrow, GA · On-site
... in accordance with training and display an acceptable level of competency with all Quality ... CCP's, GLP's, Hold/Release, and Environmental Sampling. The individual must also request additional ...
Comfort Keepers is seeking Live-In Caregivers who can elevate a senior's quality of life and deliver the best possible in-home care; making a positive difference in the daily life of our clients ...
Comfort Keepers is seeking Live-In Caregivers who can elevate a senior's quality of life and deliver the best possible in-home care; making a positive difference in the daily life of our clients ...
Live In Glp Qa information
See salary details
$38K - $50.8K
3% of jobs
$50.8K - $63.6K
6% of jobs
$63.6K - $76.5K
11% of jobs
$82K is the 25th percentile. Wages below this are outliers.
$76.5K - $89.3K
12% of jobs
$89.3K - $102.1K
11% of jobs
The median wage is $114.1K / yr.
$102.1K - $114.9K
8% of jobs
$114.9K - $127.7K
4% of jobs
$137.2K is the 75th percentile. Wages above this are outliers.
$127.7K - $140.5K
27% of jobs
$140.5K - $153.4K
1% of jobs
$153.4K - $166.2K
1% of jobs
$166.2K - $179K
16% of jobs
$38K
$118.1K
$179K
How much do live in glp qa jobs pay per year?
What is the difference between Live In Glp Qa vs Live In Glp Auditor?
| Aspect | Live In Glp Qa | Live In Glp Auditor |
|---|---|---|
| Certifications | GMP, GLP knowledge, QA certifications | GMP, GLP, QA certifications |
| Work Environment | Pharmaceutical or biotech labs, manufacturing facilities | Pharmaceutical or biotech labs, manufacturing facilities |
| Employer & Industry | Pharma companies, contract research organizations | Pharma companies, contract research organizations |
| Primary Focus | Ensuring GLP compliance in QA processes | Auditing 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.
Elanco rating
7.8
Based on 25 frontline employees who took The Breakroom Quiz
51st of 86 rated pharmaceutical
Job description
At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Your Role: Quality Assurance Associate - R&D Quality Assurance
As a Quality Assurance Associate - R&D Quality Assurance, you will support the Research & Development Clinical Development organization by providing quality oversight for regulated animal health research and development activities. In this role, you will help advance GLP compliance, quality systems oversight, and audit readiness while partnering cross-functionally to support global veterinary product approvals.
Your Responsibilities:
Support execution of the site Quality Assurance program in compliance with FDA GLP regulations, USDA requirements, and Elanco Quality Standards
Plan and conduct audits of regulated studies, systems, protocols, data, and final reports to ensure compliance with protocols, SOPs, and regulatory requirements
Provide quality oversight for third-party GLP studies, including protocol and final report review activities
Support deviations, investigations, CAPA activities, and process audits to strengthen quality systems and compliance
Assist with regulatory inspection readiness, quality training, and ongoing Quality Management System support
What You Need to Succeed (minimum qualifications):
Education: Bachelor's degree in science, Animal Science, or related field
Experience: Minimum 3 years' experience working in a regulated (GCP, GLP) research environment
Top 2 skills: Strong attention to detail and regulatory compliance mindset combined with effective communication and collaboration skills
What will give you a competitive edge (preferred qualifications):
Experience working in regulated environments such as FDA, USDA, or EPA
Experience in research laboratories, veterinary studies, or livestock production settings
Knowledge of Quality Systems and Computer System Validation processes
Experience supporting audits, investigations, or CAPA activities
Demonstrated learning agility and ability to work cross-functionally in a regulated environment
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against jobrelated criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
About Elanco
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
5,001 - 10,000 Employees
Headquarters location
Greenfield, IN, US
Year founded
1954