The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp's global network, with an immediate focus on improving ...
The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp's global network, with an immediate focus on improving ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible ...
FDA cGMP requirements * Environmental Health & Safety (EHS) * Compliance processes * Job-specific and general work skills * Actively lead and facilitate training sessions * Assist in conducting ...
Quick apply
FDA cGMP requirements * Environmental Health & Safety (EHS) * Compliance processes * Job-specific and general work skills * Actively lead and facilitate training sessions * Assist in conducting ...
cGMP Associate Director, Process Development
$130K - $140K/yr
USC's Keck School of Medicine, cGMP Department is seeking a dynamic individual to foster and enhance the translation and manufacturing of cell and gene therapies and other biological products for ...
cGMP Associate Director, Process Development
$130K - $140K/yr
USC's Keck School of Medicine, cGMP Department is seeking a dynamic individual to foster and enhance the translation and manufacturing of cell and gene therapies and other biological products for ...
Adecco Healthcare & Life Sciences is hiring a cGMP Biomanufacturing Training Specialist for our pharmaceutical/biomanufacturing partner in Madison, WI . The anticipated hourly wage for this position ...
Quick apply
Adecco Healthcare & Life Sciences is hiring a cGMP Biomanufacturing Training Specialist for our pharmaceutical/biomanufacturing partner in Madison, WI . The anticipated hourly wage for this position ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87K - $92K/yr
Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87K - $92K/yr
Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible ...
Manufacturing Associate - cGMP API Production
Groton, CT · On-site
$15 - $19/hr
Position Overview You will be a key member of a multidisciplinary manufacturing team supporting the cGMP production of non‑commercial clinical API batches . This role is hands‑on and ...
Quick apply
Manufacturing Associate - cGMP API Production
Groton, CT · On-site
$15 - $19/hr
Position Overview You will be a key member of a multidisciplinary manufacturing team supporting the cGMP production of non‑commercial clinical API batches . This role is hands‑on and ...
Global Head of cGMP Training
Allentown, PA · On-site
The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp's global network, with an immediate focus on improving ...
Global Head of cGMP Training
Allentown, PA · On-site
The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp's global network, with an immediate focus on improving ...
Global Head of cGMP Training
Allentown, PA · On-site
The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp's global network, with an immediate focus on improving ...
Global Head of cGMP Training
Allentown, PA · On-site
The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp's global network, with an immediate focus on improving ...
M-F onsite Knowledge in cGMP / GMP manufacturing and technical knowledge in validation of pharmaceutical processes/systems/equipment Project Management and organizational skills, including ability to ...
M-F onsite Knowledge in cGMP / GMP manufacturing and technical knowledge in validation of pharmaceutical processes/systems/equipment Project Management and organizational skills, including ability to ...
Engineer II
New Albany, OH · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
Quick apply
Engineer II
New Albany, OH · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
Quick apply
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
cGMP Manufacturing Supervisor - Night Shift
$88K - $152K/yr
At MilliporeSigma, as the cGMP Manufacturing Supervisor - Night Shift at our 3300 South Second Ave / Cherokee site, will manage production personnel in the manufacture of products and many support ...
cGMP Manufacturing Supervisor - Night Shift
$88K - $152K/yr
At MilliporeSigma, as the cGMP Manufacturing Supervisor - Night Shift at our 3300 South Second Ave / Cherokee site, will manage production personnel in the manufacture of products and many support ...
cGMP Manufacturing Supervisor - Night Shift
$88K - $152K/yr
At MilliporeSigma, as the cGMP Manufacturing Supervisor - Night Shift at our 3300 South Second Ave / Cherokee site, will manage production personnel in the manufacture of products and many support ...
cGMP Manufacturing Supervisor - Night Shift
$88K - $152K/yr
At MilliporeSigma, as the cGMP Manufacturing Supervisor - Night Shift at our 3300 South Second Ave / Cherokee site, will manage production personnel in the manufacture of products and many support ...
Manufacturing Associate - cGMP API Production
Groton, CT · On-site
$15 - $19/hr
Position Overview You will be a key member of a multidisciplinary manufacturing team supporting the cGMP production of non-commercial clinical API batches . This role is hands-on and process-driven ...
Manufacturing Associate - cGMP API Production
Groton, CT · On-site
$15 - $19/hr
Position Overview You will be a key member of a multidisciplinary manufacturing team supporting the cGMP production of non-commercial clinical API batches . This role is hands-on and process-driven ...
Research Technologist-cGMP Manufacturing
Buffalo, NY · On-site
$52K - $67K/yr
Research Technologist-cGMP Manufacturing Job Type: Regular Company: Health Research, Inc. (HRI) Roswell Park Division Department: Center for Immunotherapy Time Type: Full time Weekly Hours: 40 FTE: 1 ...
Research Technologist-cGMP Manufacturing
Buffalo, NY · On-site
$52K - $67K/yr
Research Technologist-cGMP Manufacturing Job Type: Regular Company: Health Research, Inc. (HRI) Roswell Park Division Department: Center for Immunotherapy Time Type: Full time Weekly Hours: 40 FTE: 1 ...
Engineer II - Nights / Weekends
Pleasant Prairie, WI · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
Engineer II - Nights / Weekends
Pleasant Prairie, WI · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
Engineer II - Nights / Weekends
Pleasant Prairie, WI · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
Quick apply
Engineer II - Nights / Weekends
Pleasant Prairie, WI · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
Engineer II
New Albany, OH · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
Engineer II
New Albany, OH · On-site
$75K - $95K/yr
About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible ...
Cgmp information
See salary details
$14.18 - $18.51
11% of jobs
$22.68 is the 25th percentile. Wages below this are outliers.
$18.51 - $22.84
15% of jobs
$22.84 - $27.16
14% of jobs
The median wage is $30.05 / hr.
$27.16 - $31.49
16% of jobs
$31.49 - $35.82
14% of jobs
$38.46 is the 75th percentile. Wages above this are outliers.
$35.82 - $40.14
10% of jobs
$40.14 - $44.47
7% of jobs
$44.47 - $48.80
5% of jobs
$48.80 - $53.13
5% of jobs
$53.13 - $57.45
2% of jobs
$57.45 - $61.78
1% of jobs
$14
$34
$61
How much do cgmp jobs pay per hour?
What is a cGMP job?
A cGMP job refers to a role that follows Current Good Manufacturing Practices (cGMP) in industries like pharmaceuticals, biotechnology, and food production. These jobs ensure products are consistently produced and controlled according to quality standards. Employees in cGMP roles follow strict guidelines for cleanliness, documentation, and compliance to maintain safety and efficacy. Common positions include quality assurance, manufacturing operators, and regulatory specialists.
What jobs pay 2000 a day?
What is the work of CGMP?
What jobs pay $10,000 a month without a degree?
What are the key skills and qualifications needed to thrive in the Cgmp position, and why are they important?
To thrive in a cGMP (Current Good Manufacturing Practices) role, you need a strong understanding of pharmaceutical or biotechnology manufacturing processes, quality control, and regulatory compliance, typically supported by a degree in life sciences or engineering. Familiarity with quality management systems (QMS), documentation protocols, and certifications like Six Sigma or cGMP training is highly beneficial. Attention to detail, teamwork, and strong communication skills are important for collaborating in cross-functional environments and ensuring compliance. These skills are critical for maintaining product safety, meeting regulatory standards, and supporting efficient manufacturing operations.
What are common challenges faced in cGMP roles within pharmaceutical manufacturing?
Professionals working in cGMP roles often encounter challenges such as maintaining strict compliance with regulatory standards and adapting to frequent updates in guidelines. Attention to detail is essential, as even small errors in documentation or process execution can have significant consequences for product safety and compliance. Team members must work effectively across departments like quality assurance, production, and regulatory affairs to troubleshoot deviations and implement corrective actions. Successful cGMP professionals embrace continuous learning and adaptability to thrive amidst evolving industry requirements and technologies.
What jobs in the US pay 300,000 a year?

Full-time
Posted 5 days ago
Job description
SUMMARY:
The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp's global network, with an immediate focus on improving shop floor and operational training.
This role is accountable for raising the quality, relevance, and consistency of training for GMPimpacting roles, particularly within manufacturing, packaging, labeling, laboratory, and warehousing operations. The emphasis of the role is to mature training beyond foundational and task-based to smarter and more effective learning that improves performance, decisionmaking, and inspection readiness.
Success in this role will come from working with site Quality and Operations leaders to improve how training is designed, delivered, and sustained especially at the shop floor level, while ensuring solutions remain fitforpurpose, scalable, and sustainable.
A critical focus of the role is strengthening trainers and onthejob training, ensuring that those delivering training are not only technically competent, but are also effective communicators of the "why" behind cGMP requirements, process controls, and data integrity expectations.
ESSENTIAL DUTIES & RESPONSIBILITIES:
NearTerm Training Improvement Focus
- Assess the current state of GMP training at Sharp, with specific emphasis on shop floor, operational, and laboratory roles, using a riskbased and pragmatic lens.
- Identify specific, highimpact gaps where improved training will meaningfully reduce deviations, rightfirsttime errors, rework, and inspection risk.
- Establish a focused, phased improvement roadmap that prioritizes:
- GMP activities related to critical GMP roles
- GMP activities and processes that are highrisk.
- Sites or functions with opportunities in training and learning
- Using communities of practice to share practical learning and best practices across sites, without creating unnecessary structure or overhead.
- Avoid overengineering or largescale redesigns in the near term; prioritize incremental, practical improvement that can be implemented and sustained.
OntheJob Training (OJT) & Trainer Capability
- Define which elements of key roles require structured, formalized OJT, prioritizing those with direct impact on:
- Product quality
- Patient safety
- Regulatory compliance
- Develop simple, consistent OJT frameworks that:
- Are clear and usable on the shop floor.
- Focus on both what to do and why it matters.
- Can be adapted locally based on process complexity and risk.
- Establish clear and realistic expectations for trainer qualification, including:
- Technical competence in the process
- Ability to explain underlying cGMP principles.
- Understanding of data integrity and regulatory expectations
- Strengthen the capability of trainers as communicators, not just task demonstrators, raising the overall quality of knowledge transfer and retention.
Use of Smart Digital & ComputerBased Training
- Lead the practical deployment and optimization of Veeva's Training 2.0 - Sharp's global training administration and learning platform.
- Expand the use of computerbased and blended learning (combining classroom instruction with online/asynchronous digital learning), particularly for:
- Foundational cGMP concepts
- Refresher training
- Common, repeatable learning needs
- Drive digital learning to be:
- Clear, concise, and relevant
- Designed for the realities of the shop floor environment.
- Used to support handson training.
- Explore targeted, lowcomplexity uses of emerging technology (including AI) only where it clearly improves efficiency or effectiveness, avoiding experimental or administrative burden.
Training Effectiveness & Performance Impact
- Move training evaluation beyond completion metrics to simple, meaningful indicators, such as:
- Trends in deviations and repeat errors
- Quality events linked to training gaps
- Rightfirsttime and execution errors
- Work with sites to diagnose where training quality, not just adherence, is contributing to performance issues and implement focused, practical improvements.
- Ensure training improvements are deliberately linked to PQS maturity, process robustness, and inspection readiness, consistent with Sharp's quality priorities.
Stakeholder Partnership & Governance
- Operate as a corporate enabler and coach, not a centralized owner of site training execution.
- Provide clear guidance and practical tools aligned with Global Quality Standards while respecting site accountability.
- Maintain awareness of evolving regulatory expectations for:
- Qualified trainers
- Training effectiveness
- Workforce capability
while ensuring solutions remain operationally realistic and sustainable.
SUPERVISORY RESPONSIBILITIES:
None
EDUCATION AND EXPERIENCE:
- Bachelor's degree in Life Sciences, Engineering, Quality, or a related discipline, or equivalent combination of education and relevant cGMP experience.
- Minimum of 8-12 years of experience in pharmaceutical or regulated environments, with a strong foundation in cGMP operations and quality systems.
- Demonstrated experience in training, learning, or capability development, particularly within manufacturing, packaging, laboratory, or operational settings.
- Experience implementing or improving training effectiveness, including on-the-job training (OJT), trainer capability, and/or digital learning solutions preferred.
- Strong working knowledge of cGMP regulations, data integrity principles, and Pharmaceutical Quality Systems.
- Ability to translate regulatory requirements into practical, shop floor-ready training approaches.
- Proven ability to influence across sites and functions without direct authority.
PHYSICAL DEMANDS:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
The employee frequently is required to sit. The employee is occasionally required to stand, walk, and reach with hands and arms. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus.
WORK ENVIRONMENT:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is normally required to sit at a desk or periodically go onto the shop floor. The working environment is clean and not normally subject to hazardous environment or conditions.
Travel to customers on an as needed basis.
DISCLAIMER:
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.