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Glp Jobs (NOW HIRING)

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 ...

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 Overview The incumbent/appointee will be responsible for ensuring that ...

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 ...

Be Seen First

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 ...

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Glp information

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$5

$22

$64

How much do glp jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for glp in the United States is $22.90, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

How to make 80000 a year without a degree?

A GLP (General Labor Position) can potentially earn $80,000 annually through experience, overtime, and high-demand industries such as construction or manufacturing. Developing skills, gaining certifications, and working in environments with premium pay can increase earning potential without a degree.

What are some common challenges faced by professionals working in GLP (Good Laboratory Practice) roles, and how can they be addressed?

Professionals in GLP roles often encounter challenges such as maintaining meticulous documentation, ensuring strict protocol adherence, and staying updated with evolving regulatory standards. These responsibilities require strong attention to detail and effective time management. Collaboration with cross-functional teams, such as quality assurance and laboratory staff, is essential to ensure compliance and data integrity. Regular training and open communication channels can help address these challenges and support a smooth workflow.

What jobs pay $10,000 a month without a degree?

High-paying jobs that can reach $10,000 a month without a degree include roles such as sales managers, real estate brokers, commercial pilots, and skilled trades like electricians or plumbers. Success in these fields often depends on experience, certifications, or licensing, rather than formal education, and they may require strong interpersonal skills or technical expertise.

What jobs pay 2000 a day?

High-paying jobs that can pay around $2,000 a day typically include specialized roles such as surgeons, anesthesiologists, corporate lawyers, and certain high-level consultants or traders. These positions often require advanced education, certifications, extensive experience, and work in demanding environments or industries like healthcare, finance, or law. Earnings can vary based on location, workload, and individual performance.

What is the difference between Glp vs Pharmacist?

AspectGlpPharmacist
Required CredentialsCertification in Good Laboratory Practice (GLP) standardsDoctor of Pharmacy (PharmD) or equivalent, licensure
Work EnvironmentLaboratories, research facilitiesPharmacies, hospitals, clinics
Industry UsageRegulatory compliance, research oversightMedication dispensing, patient care
Common Search/ComparisonGLP vs PharmacistPharmacist 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?

GLP professionals are individuals who ensure that laboratory studies are conducted in accordance with Good Laboratory Practice regulations. These standards are designed to ensure the quality, reliability, and integrity of non-clinical laboratory studies, particularly those related to the safety of pharmaceuticals, chemicals, and other products. GLP professionals may work in various roles, such as quality assurance, study direction, data management, or laboratory operations. Their responsibilities include maintaining documentation, overseeing compliance, and supporting audits or inspections. By adhering to GLP guidelines, they help ensure that data generated in the lab are credible and accepted by regulatory agencies.

What are the key skills and qualifications needed to thrive as a GLP (Good Laboratory Practice) Specialist, and why are they important?

To thrive as a GLP Specialist, you need a solid background in laboratory sciences, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in GLP environments. Familiarity with laboratory information management systems (LIMS), audit processes, and documentation standards is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure data integrity, regulatory compliance, and the smooth operation of laboratory processes subject to strict guidelines.

What jobs in the US pay 300,000 a year?

High-paying jobs that can reach or exceed $300,000 annually include roles such as senior corporate executives, specialized physicians, anesthesiologists, surgeons, and certain investment bankers or hedge fund managers. These positions often require advanced degrees, extensive experience, and strong skills in leadership, finance, or healthcare. Compensation varies based on industry, location, and individual performance.
More about Glp jobs
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What states have the most Glp jobs? States with the most job openings for Glp jobs include:
GLP Quality Assurance Specialist

GLP Quality Assurance Specialist

Clorox

Pleasanton, CA โ€ข Hybrid

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.