Assists with internal quality assurance program for preclinical GLP studies. Conducts internal and ... Supports preclinical teams in gathering and reporting various performance metrics * Plans ...
New
Assists with internal quality assurance program for preclinical GLP studies. Conducts internal and ... Supports preclinical teams in gathering and reporting various performance metrics * Plans ...
New
Assists with internal quality assurance program for preclinical GLP studies. Conducts internal and ... Supports preclinical teams in gathering and reporting various performance metrics * Plans ...
New
... in pharmaceutical, biotech or medical device industry * Strong knowledge of GMP, GLP, and ... QA support) #LI-LM1
... in pharmaceutical, biotech or medical device industry * Strong knowledge of GMP, GLP, and ... QA support) #LI-LM1
Chicago, IL · On-site
$65K - $75K/yr
QA Specialist/Auditor Title: QA Specialist/Auditor Location: Chicago, IL Reports to : Senior ... in the conduct of GLP audits. Salary: $65-75k Benefits: * 401k Employer Match with immediate ...
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Chicago, IL · On-site
$65K - $75K/yr
QA Specialist/Auditor Title: QA Specialist/Auditor Location: Chicago, IL Reports to : Senior ... in the conduct of GLP audits. Salary: $65-75k Benefits: * 401k Employer Match with immediate ...
Washington, DC · On-site
$22.50 - $30.95/hr
... Part 58 GLP) * Interest and ability to learn and apply new skills in multiple subject areas ... Live an Extraordinary Life We care about your well-being, not just on the job. Battelle offers ...
Washington, DC · On-site
$22.50 - $30.95/hr
... Part 58 GLP) * Interest and ability to learn and apply new skills in multiple subject areas ... Live an Extraordinary Life We care about your well-being, not just on the job. Battelle offers ...
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 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 ...
Weyauwega, WI · On-site
$102K - $128K/yr
We believe in working together, speaking honestly, taking ownership, and creating value in ... Ability to read, understand, and follow documents and procedures (GLP, SOP, MSDS, GMP, test ...
Weyauwega, WI · On-site
$102K - $128K/yr
We believe in working together, speaking honestly, taking ownership, and creating value in ... Ability to read, understand, and follow documents and procedures (GLP, SOP, MSDS, GMP, test ...
... 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 ...
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... 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 ...
Portland, OR · On-site
Excellent in other OMIC's performance factors * Highly competent user of MS Office * Registered Quality Assurance Professional (RQAP) * Registered Quality Assurance Professional for GLP regulations ...
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Portland, OR · On-site
Excellent in other OMIC's performance factors * Highly competent user of MS Office * Registered Quality Assurance Professional (RQAP) * Registered Quality Assurance Professional for GLP regulations ...
Weyauwega, WI · On-site
$102K - $128K/yr
We believe in working together, speaking honestly, taking ownership, and creating value in ... Ability to read, understand, and follow documents and procedures (GLP, SOP, MSDS, GMP, test ...
Weyauwega, WI · On-site
$102K - $128K/yr
We believe in working together, speaking honestly, taking ownership, and creating value in ... Ability to read, understand, and follow documents and procedures (GLP, SOP, MSDS, GMP, test ...
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 ...
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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 ...
Portland, OR · On-site
Excellent in other OMIC's performance factors * Highly competent user of MS Office * Registered Quality Assurance Professional (RQAP) * Registered Quality Assurance Professional for GLP regulations ...
Quick apply
Portland, OR · On-site
Excellent in other OMIC's performance factors * Highly competent user of MS Office * Registered Quality Assurance Professional (RQAP) * Registered Quality Assurance Professional for GLP regulations ...
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 ...
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 ...
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 ...
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 ...
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 ...
Bedford, MA · On-site
$109K - $121K/yr
The Senior Associate, QA will work in collaboration with all departments within Ocular, to provide ... in pharmaceutical, biotech or medical device industry * Strong knowledge of GMP, GLP, and ...
Bedford, MA · On-site
$109K - $121K/yr
The Senior Associate, QA will work in collaboration with all departments within Ocular, to provide ... in pharmaceutical, biotech or medical device industry * Strong knowledge of GMP, GLP, and ...
NC · On-site
$34/hr
This position will report to the Quality Assurance Manager (GCP/GLP). Job Responsibilities ... Perform in-process inspections of nonclinical study phases and assay methods. * Review study events ...
NC · On-site
$34/hr
This position will report to the Quality Assurance Manager (GCP/GLP). Job Responsibilities ... Perform in-process inspections of nonclinical study phases and assay methods. * Review study events ...
... 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 ...
Provide assistance or support to other Inotiv QA team members as necessary * Perform other duties ... Three to five years of experience in a GLP preferably with 1-3 or more years of auditing experience ...
Provide assistance or support to other Inotiv QA team members as necessary * Perform other duties ... Three to five years of experience in a GLP preferably with 1-3 or more years of auditing experience ...
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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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 ...
$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
| 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.
8.5
Based on 119 frontline employees who took The Breakroom Quiz
33rd of 528 rated manufacturers
Recruiter: Spencer Gregory Hale
Sr Preclinical Quality Auditor
About the role:
Assists with internal quality assurance program for preclinical GLP studies. Conducts internal and external GLP quality audits to assure that BSC preclinical trials comply with all applicable regulatory requirements, standards and BSC policies and procedures. Supports Inspection Readiness and Preclinical Corrective and Preventative Action (CAPA).
Your responsibilities include:
What we’re looking for in you:
Minimum Requirements
Preferred Qualifications:
Requisition ID: 631336
Minimum Salary: $85000
Maximum Salary: $161500
The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.
Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
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