GLP standards require implementation of a robust quality management system to ensure the validity, integrity and reliability of data submitted for regulatory evaluation and EPA approval. A QAU exists ...
GLP standards require implementation of a robust quality management system to ensure the validity, integrity and reliability of data submitted for regulatory evaluation and EPA approval. A QAU exists ...
Sr. Manager, CQA GLP
Somerset, NJ ยท Hybrid
Legend Biotech is seeking a Manager/Sr. Manager, GLP - CQA as part of the Regulatory Affairs team based in Somerset, NJ . Role Overview The incumbent/appointee will be responsible for ensuring that ...
Sr. Manager, CQA GLP
Somerset, NJ ยท Hybrid
Legend Biotech is seeking a Manager/Sr. Manager, GLP - CQA as part of the Regulatory Affairs team based in Somerset, NJ . Role Overview The incumbent/appointee will be responsible for ensuring that ...
Legend Biotech is seeking a Manager/Sr. Manager, GLP - CQA as part of the Regulatory Affairs team based in Somerset, NJ.Role OverviewThe incumbent/appointee will be responsible for ensuring that the ...
Legend Biotech is seeking a Manager/Sr. Manager, GLP - CQA as part of the Regulatory Affairs team based in Somerset, NJ.Role OverviewThe incumbent/appointee will be responsible for ensuring that the ...
GLP standards require implementation of a robust quality management system to ensure the validity, integrity and reliability of data submitted for regulatory evaluation and EPA approval. A QAU exists ...
GLP standards require implementation of a robust quality management system to ensure the validity, integrity and reliability of data submitted for regulatory evaluation and EPA approval. A QAU exists ...
GLP standards require implementation of a robust quality management system to ensure the validity, integrity and reliability of data submitted for regulatory evaluation and EPA approval. A QAU exists ...
GLP standards require implementation of a robust quality management system to ensure the validity, integrity and reliability of data submitted for regulatory evaluation and EPA approval. A QAU exists ...
Sr. Manager, CQA GLP
Somerset, NJ ยท On-site
Legend Biotech is seeking a Manager/Sr. Manager, GLP - CQA as part of the Regulatory Affairs team based in Somerset, NJ . Role Overview The incumbent/appointee will be responsible for ensuring that ...
Sr. Manager, CQA GLP
Somerset, NJ ยท On-site
Legend Biotech is seeking a Manager/Sr. Manager, GLP - CQA as part of the Regulatory Affairs team based in Somerset, NJ . Role Overview The incumbent/appointee will be responsible for ensuring that ...
The Director GLP QA performs and/or manages vendor audits including: * Development of the audit plan, audit conduct, and reporting * Tracking and coordination of audit closure tasks including review ...
The Director GLP QA performs and/or manages vendor audits including: * Development of the audit plan, audit conduct, and reporting * Tracking and coordination of audit closure tasks including review ...
The Director GLP QA performs and/or manages vendor audits including: * Development of the audit plan, audit conduct, and reporting * Tracking and coordination of audit closure tasks including review ...
The Director GLP QA performs and/or manages vendor audits including: * Development of the audit plan, audit conduct, and reporting * Tracking and coordination of audit closure tasks including review ...
Ginning Leadership Program - (GLP)
Savannah, GA ยท On-site
$35K - $44K/yr
GLP moves young professionals through different roles and tasks within Lummus Corporation to develop new skills and bring a new perspective to existing work. Each participant will be trained for ...
Ginning Leadership Program - (GLP)
Savannah, GA ยท On-site
$35K - $44K/yr
GLP moves young professionals through different roles and tasks within Lummus Corporation to develop new skills and bring a new perspective to existing work. Each participant will be trained for ...
Ginning Leadership Program - (GLP)
Savannah, GA ยท On-site
$35K - $44K/yr
GLP moves young professionals through different roles and tasks within Lummus Corporation to develop new skills and bring a new perspective to existing work. Each participant will be trained for ...
Ginning Leadership Program - (GLP)
Savannah, GA ยท On-site
$35K - $44K/yr
GLP moves young professionals through different roles and tasks within Lummus Corporation to develop new skills and bring a new perspective to existing work. Each participant will be trained for ...
GLP Technical Support Specialist
$62K - $69K/yr
Cape Fox subsidiary Eagle Health, LLC is accepting resumes for a GLP Technical Support Specialist to support the members at Ft. Detrick, Maryland. This position is contingent upon contract award.
GLP Technical Support Specialist
$62K - $69K/yr
Cape Fox subsidiary Eagle Health, LLC is accepting resumes for a GLP Technical Support Specialist to support the members at Ft. Detrick, Maryland. This position is contingent upon contract award.
The Senior Manager will lead GLP quality oversight for regulated non-clinical studies and external partners, ensuring compliance, documentation integrity, and inspection readiness. This individual ...
The Senior Manager will lead GLP quality oversight for regulated non-clinical studies and external partners, ensuring compliance, documentation integrity, and inspection readiness. This individual ...
The Senior Manager will lead GLP quality oversight for regulated non-clinical studies and external partners, ensuring compliance, documentation integrity, and inspection readiness. This individual ...
The Senior Manager will lead GLP quality oversight for regulated non-clinical studies and external partners, ensuring compliance, documentation integrity, and inspection readiness. This individual ...
Director, GLP Quality Assurance & Compliance Building a Culture of Quality & Compliance in a Leading In Vivo Research Facility Company Overview We are a pioneering research organization dedicated to ...
Quick apply
Director, GLP Quality Assurance & Compliance Building a Culture of Quality & Compliance in a Leading In Vivo Research Facility Company Overview We are a pioneering research organization dedicated to ...
The Director and Head of GCP/GVP/GLP Quality is a leadership role responsible for both strategic and operational oversight of GCP, GVP, and GLP Quality activities. The responsibilities include goal ...
The Director and Head of GCP/GVP/GLP Quality is a leadership role responsible for both strategic and operational oversight of GCP, GVP, and GLP Quality activities. The responsibilities include goal ...
GLP Study Director - In Vivo Services
Hercules, CA ยท On-site
$120K - $150K/yr
Pacific BioLabs is an independent CRO providing cGMP/GLP testing in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology. We are currently hiring to support our clients ...
GLP Study Director - In Vivo Services
Hercules, CA ยท On-site
$120K - $150K/yr
Pacific BioLabs is an independent CRO providing cGMP/GLP testing in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology. We are currently hiring to support our clients ...
GLP Study Director - In Vivo Services
Hercules, CA ยท On-site
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PBL has immediate openings for full time GLP Study Director in the In Vivo Services Department. As the single point of study management and control, GLP Study Director will be responsible for the ...
GLP Study Director - In Vivo Services
Hercules, CA ยท On-site
$120K - $150K/yr
PBL has immediate openings for full time GLP Study Director in the In Vivo Services Department. As the single point of study management and control, GLP Study Director will be responsible for the ...
Be Seen First
Weight Loss Coordinator (GLP)
Miami Shores, FL ยท On-site
$21 - $25/hr
Job Overview We are looking for a Weight Loss Coordinator (GLP) to lead our weight management programs. In this role, you will serve as a vital link between clients and our health team, guiding ...
Quick apply
Be Seen First
Weight Loss Coordinator (GLP)
Miami Shores, FL ยท On-site
$21 - $25/hr
Job Overview We are looking for a Weight Loss Coordinator (GLP) to lead our weight management programs. In this role, you will serve as a vital link between clients and our health team, guiding ...
GLP Study Director - In Vivo Services
Hercules, CA ยท On-site
$120K - $150K/yr
PBL has immediate openings for full time GLP Study Director in the In Vivo Services Department. As the single point of study management and control, GLP Study Director will be responsible for the ...
GLP Study Director - In Vivo Services
Hercules, CA ยท On-site
$120K - $150K/yr
PBL has immediate openings for full time GLP Study Director in the In Vivo Services Department. As the single point of study management and control, GLP Study Director will be responsible for the ...
GLP Quality Assurance Manager, Contract Research Organization
Scranton, PA ยท Remote
$90K - $115K/yr
Quality Assurance Manager GLP About the Role: The Quality Assurance Manager is responsible for managing daily QA activities and leading a small team of QA Associates. Reporting remotely to the QA ...
Quick apply
GLP Quality Assurance Manager, Contract Research Organization
Scranton, PA ยท Remote
$90K - $115K/yr
Quality Assurance Manager GLP About the Role: The Quality Assurance Manager is responsible for managing daily QA activities and leading a small team of QA Associates. Reporting remotely to the QA ...
Glp information
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$5.29 - $10.69
0% of jobs
$12.56 is the 25th percentile. Wages below this are outliers.
$10.69 - $16.08
72% of jobs
$16.96 is the 75th percentile. Wages above this are outliers.
$16.08 - $21.48
18% of jobs
$21.48 - $26.88
0% of jobs
$26.88 - $32.28
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$32.28 - $37.67
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$37.67 - $43.07
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$43.07 - $48.47
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$48.47 - $53.87
2% of jobs
$53.87 - $59.27
4% of jobs
$59.27 - $64.66
4% of jobs
$5
$22
$64
How much do glp jobs pay per hour?
How to make 80000 a year without a degree?
What are some common challenges faced by professionals working in GLP (Good Laboratory Practice) roles, and how can they be addressed?
What jobs pay $10,000 a month without a degree?
What jobs pay 2000 a day?
What is the difference between Glp vs Pharmacist?
| Aspect | Glp | Pharmacist |
|---|---|---|
| Required Credentials | Certification in Good Laboratory Practice (GLP) standards | Doctor of Pharmacy (PharmD) or equivalent, licensure |
| Work Environment | Laboratories, research facilities | Pharmacies, hospitals, clinics |
| Industry Usage | Regulatory compliance, research oversight | Medication dispensing, patient care |
| Common Search/Comparison | GLP vs Pharmacist | Pharmacist roles, responsibilities |
GLP professionals focus on ensuring laboratory compliance with regulatory standards in research settings, while pharmacists are healthcare providers responsible for dispensing medications and advising patients. Both roles require specialized knowledge but serve different functions within the healthcare and research industries.
What are GLP (Good Laboratory Practice) professionals?
What are the key skills and qualifications needed to thrive as a GLP (Good Laboratory Practice) Specialist, and why are they important?
What jobs in the US pay 300,000 a year?
Full-time
Medical, Retirement, PTO
Posted 15 days ago
Job description
Clorox is the place that's committed to growth - for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlace
Your role at Clorox:
As a Scientist II in Global Stewardship / Regulatory, you will be part of the Quality Assurance Unit (QAU) with responsibility for Good Laboratory Practice (GLP), working with a cross functional team to generate quality data and documentation for business critical Regulatory submissions to the US Environmental Protection Agency (EPA). This critical work is a key driver for delivering Cleaning Business objectives and enables health of the Cleaning Business.Federal regulations require the use of Good Laboratory Practices (GLP) for conducting studies that support or are intended to support applications for research or marketing permits for pesticide products regulated by the EPA. GLP standards require implementation of a robust quality management system to ensure the validity, integrity and reliability of data submitted for regulatory evaluation and EPA approval.
A QAU exists to assure management that facilities, personnel, practices and records are in compliance with regulations, to maintain a master schedule sheet of studies, to inspect each study at intervals to assure compliance and to report findings to Study Director, Study Sponsors and Management.
This role is focused on 40 CFR Part 160 (EPA-GLP) compliance of product chemistry studies related to testing of antimicrobial products.
This position will be located in our Pleasanton, CA office, and the individual will be expected to be in the office of 3 days a week.
In this role, you will:
Program Management
As the QAU:
Collaborate within the QAU and with GLP staff to develop and implement improvements for overall test facility compliance
Provide input to management via quarterly updates
Auditing
Be responsible for the inspection of protocols, in-process testing, data/draft reports, final reports
Coordinate CPC annual facility self-assessment and contract labs inspections. Communicate observations and implement changes as needed
Identify and drive improvements and efficiencies within the auditing process
Training/Guidance
Lead training for GLP personnel
Provide guidance on GLP regulations/requirements for each GLP study as needed
Improve training materials and experience to better prepare users for GLP
Study-Specific Activities (excluding auditing)
Define studies and set timing with GLP product team members
Review draft protocols, deviations, amendments, and study notes and provide input and guidance on format/content
Generate and distribute inspection reports to Study Director & management
Review revised data/report to ensure all audit findings are appropriately addressed
Sign final report QA statement
Identify, develop and champion improvements to study-specific activities
Other
Represent Clorox during EPA inspections
Monitor and implement new processes to address changes in regulations or internal practices
Interact w/ contract laboratories on QA/GLP issues
Update and issue Master Schedule
Review and provide input on draft SOPs
Maintain QAU files
Seek to continuously find opportunities to improve GLP activities
What we look for:
Bachelor or Masters degree in Chemistry or other related Science discipline or a Quality-oriented education.
2-4 years laboratory, quality or plant work experience
Analytical skills and knowledge
Good Laboratory Practice (GLP) or Good Manufacturing Process (GMP) experience
Desired:
Knowledge of 40 CFR Part 160 regulations, analytical techniques (including, but not limited to, manual titration, LC and GC), familiarity with CPG product development, micro and toxicity testing is desired.
Skills & Abilities:
Strategic thinking and ability to increase the quality-consciousness of employees by your persuasiveness
Customer and quality focused, team spirit and integrity
Experience representing GLP compliance in a cross-functional team setting and project management experience
Ability to understand and interpret GLP regulations and technical documents
Ability to work independently and collaboratively in a fast-paced, cross-functional team environment
Effectively manage multiple priorities; results-oriented; process-driven
High attention to detail
Flexible and adaptable to changing business needs and priorities
Strong oral and written communication skills with ability to engage and influence various audiences at multiple levels in the organization
Excellent planning, organizational, and time management skills with attention to detail
Some travel may be required (approximately 5%)
#LI-Hybrid
Workplace type:
This position will be located in our Pleasanton, CA office, and the individual will be expected to be in the office of 3 days a week.Our values-based culture connects to our purpose and empowers people to be their best, professionally and personally. We serve a diverse consumer base which is why we believe teams that reflect our consumers bring fresh perspectives, drive innovation, and help us stay attuned to the world around us. That's why we foster an inclusive culture where every person can feel respected, valued, and fully able to participate, and ultimately able to thrive. Learn more.
[U.S.]Additional Information:
At Clorox, we champion people to be well and thrive, starting with our own people. To help make this possible, we offer comprehensive, competitive benefits that prioritize all aspects of wellbeing and provide flexibility for our teammates' unique needs. This includes robust health plans, a market-leading 401(k) program with a company match, flexible time off benefits (including half-day summer Fridays depending on location), inclusive fertility/adoption benefits, and more.
We are committed to fair and equitable pay and are transparent with current and future teammates about our full salary ranges. We use broad salary ranges that reflect the competitive market for similar jobs, provide sufficient opportunity for growth as you gain experience and expand responsibilities, while also allowing for differentiation based on performance. Based on the breadth of our ranges, most new hires will start at Clorox in the first half of the applicable range. Your starting pay will depend on job-related factors, including relevant skills, knowledge, experience and location. The applicable salary range for every role in the U.S. is based on your work location and is aligned to one of three zones according to the cost of labor in your area.
-Zone A: $88,700 - $165,900
-Zone B: $81,300 - $152,100
-Zone C: $73,900 - $138,300
All ranges are subject to change in the future. Your recruiter can share more about the specific salary range for your location during the hiring process.
This job is also eligible for participation in Clorox's incentive plans, subject to the terms of the applicable plan documents and policies.
Please apply directly to our job postings and do not submit your resume to any person via text message. Clorox does not conduct text-based interviews and encourages you to be cautious of anyone posing as a Clorox recruiter via unsolicited texts during these uncertain times.
To all recruitment agencies: Clorox (and its brand families) does not accept agency resumes. Please do not forward resumes to Clorox employees, including any members of our leadership team. Clorox is not responsible for any fees related to unsolicited resumes.