QC Chemist
Cranbury, NJ · On-site
$36 - $40/hr
Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and ... Experience with Empower, LIMS, or similar systems * Strong documentation, data integrity (ALCOA ...
QC Chemist
Cranbury, NJ · On-site
$36 - $40/hr
Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and ... Experience with Empower, LIMS, or similar systems * Strong documentation, data integrity (ALCOA ...
... Pharmaceutical, Quality Management Systems Note: This description is not intended to be all ... inclusive, or a limitation of the duties of the position. It is intended to describe the general ...
Quick apply
... Pharmaceutical, Quality Management Systems Note: This description is not intended to be all ... inclusive, or a limitation of the duties of the position. It is intended to describe the general ...
... pharmaceutical experience in Quality Systems or relevant area preferred. • 1-3 years of experience with MS Word, Excel, and PowerPoint preferred. • 1-2 years project management and coordinator ...
... pharmaceutical experience in Quality Systems or relevant area preferred. • 1-3 years of experience with MS Word, Excel, and PowerPoint preferred. • 1-2 years project management and coordinator ...
... pharmaceutical experience in Quality Systems or relevant area preferred. • 1-3 years of experience with MS Word, Excel, and PowerPoint preferred. • 1-2 years project management and coordinator ...
... pharmaceutical experience in Quality Systems or relevant area preferred. • 1-3 years of experience with MS Word, Excel, and PowerPoint preferred. • 1-2 years project management and coordinator ...
Quality Systems Manager
Schaumburg, IL · On-site
$110K - $129K/yr
This is a hands-on management role with responsibility for quality system processes, QA functions ... Experience in a medical device, pharmaceutical, or regulated manufacturing environment. * Internal ...
Quality Systems Manager
Schaumburg, IL · On-site
$110K - $129K/yr
This is a hands-on management role with responsibility for quality system processes, QA functions ... Experience in a medical device, pharmaceutical, or regulated manufacturing environment. * Internal ...
Quality Systems Manager
Schaumburg, IL · On-site
$110K - $129K/yr
This is a hands-on management role with responsibility for quality system processes, QA functions ... Experience in a medical device, pharmaceutical, or regulated manufacturing environment. * Internal ...
Quality Systems Manager
Schaumburg, IL · On-site
$110K - $129K/yr
This is a hands-on management role with responsibility for quality system processes, QA functions ... Experience in a medical device, pharmaceutical, or regulated manufacturing environment. * Internal ...
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Quality System Specialist
Cabool, MO · On-site
General Purpose: The Quality Systems Specialist is responsible for maintaining training ... Serve as a member of the Food Defense and Crisis Management Teams and support related initiatives.
Quality System Specialist
Cabool, MO · On-site
General Purpose: The Quality Systems Specialist is responsible for maintaining training ... Serve as a member of the Food Defense and Crisis Management Teams and support related initiatives.
Oversee core quality system processes, including change control, training, management review, quality planning, and quality metrics. * Monitor quality system performance, identify trends, and drive ...
Oversee core quality system processes, including change control, training, management review, quality planning, and quality metrics. * Monitor quality system performance, identify trends, and drive ...
Quality System Specialist
Cabool, MO · On-site
General Purpose: The Quality Systems Specialist is responsible for maintaining training ... Serve as a member of the Food Defense and Crisis Management Teams and support related initiatives.
New
Quality System Specialist
Cabool, MO · On-site
General Purpose: The Quality Systems Specialist is responsible for maintaining training ... Serve as a member of the Food Defense and Crisis Management Teams and support related initiatives.
New
Quality System Specialist
Cabool, MO · On-site
General Purpose: The Quality Systems Specialist is responsible for maintaining training ... Serve as a member of the Food Defense and Crisis Management Teams and support related initiatives.
New
Quality System Specialist
Cabool, MO · On-site
General Purpose: The Quality Systems Specialist is responsible for maintaining training ... Serve as a member of the Food Defense and Crisis Management Teams and support related initiatives.
New
Quality System Engineer
Jupiter, FL · On-site
Further develop and ensure implementation of document management policy, audit process documentation, and other quality management system documentation. * Develop and regularly communicate the audit ...
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Quality System Engineer
Jupiter, FL · On-site
Further develop and ensure implementation of document management policy, audit process documentation, and other quality management system documentation. * Develop and regularly communicate the audit ...
Manager Quality Systems
Snoqualmie, WA · On-site
$150K - $175K/yr
Manage control of Quality Management System changes. * Manage the document control process. * Ensure staff training and competency to ensure adequate and effective QMS performance. * Facilitate ...
Manager Quality Systems
Snoqualmie, WA · On-site
$150K - $175K/yr
Manage control of Quality Management System changes. * Manage the document control process. * Ensure staff training and competency to ensure adequate and effective QMS performance. * Facilitate ...
... of pharmaceutical experience in Quality Systems or relevant area preferred. 1-3 years of experience with MS Word, Excel, and PowerPoint preferred. 1-2 years project management and coordinator ...
... of pharmaceutical experience in Quality Systems or relevant area preferred. 1-3 years of experience with MS Word, Excel, and PowerPoint preferred. 1-2 years project management and coordinator ...
The ideal candidate will be responsible for managing the quality systems, including deviations ... Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality ...
The ideal candidate will be responsible for managing the quality systems, including deviations ... Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality ...
Manage quality system documentation, procedures, work instructions, and records. * Ensure ongoing compliance through audits, management reviews, and continuous improvement initiatives. * Lead ...
Manage quality system documentation, procedures, work instructions, and records. * Ensure ongoing compliance through audits, management reviews, and continuous improvement initiatives. * Lead ...
Being a proactive and versatile team member is crucial, as is the ability to skillfully manage ... pharmaceuticals, retail/apparel, and more. More about us: Join us -- #It's all right there.
Being a proactive and versatile team member is crucial, as is the ability to skillfully manage ... pharmaceuticals, retail/apparel, and more. More about us: Join us -- #It's all right there.
The ideal candidate will be responsible for managing the quality systems, including deviations ... Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality ...
The ideal candidate will be responsible for managing the quality systems, including deviations ... Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality ...
Revolution Medicines is seeking a motivated individual with a pharmaceutical quality assurance and computer system validation (CSV) background to play a critical role as Senior Manager, IS Quality ...
Revolution Medicines is seeking a motivated individual with a pharmaceutical quality assurance and computer system validation (CSV) background to play a critical role as Senior Manager, IS Quality ...
The ideal candidate will be responsible for managing the quality systems, including deviations ... Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality ...
Quick apply
The ideal candidate will be responsible for managing the quality systems, including deviations ... Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality ...
Pharmaceutical Quality System Manager information
See salary details
$54K - $63.1K
8% of jobs
$63.1K - $72.2K
12% of jobs
$75.2K is the 25th percentile. Wages below this are outliers.
$72.2K - $81.3K
17% of jobs
The median wage is $89.4K / yr.
$81.3K - $90.4K
15% of jobs
$90.4K - $99.5K
12% of jobs
$99.5K - $108.5K
6% of jobs
$117.2K is the 75th percentile. Wages above this are outliers.
$108.5K - $117.6K
5% of jobs
$117.6K - $126.7K
6% of jobs
$126.7K - $135.8K
13% of jobs
$135.8K - $144.9K
3% of jobs
$144.9K - $154K
2% of jobs
$54K
$98.6K
$154K
How much do pharmaceutical quality system manager jobs pay per year?
As of Jul 13, 2026, the average yearly pay for pharmaceutical quality system manager in the United States is $98,613.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $122,500.00 per year, depending on experience, location, and employer.
$36 - $40/hr
Contractor
Medical, Dental, Vision, Life, Retirement
Posted 23 days ago
Job description
Job Title: QC Chemist (cGMP / HPLC / Solid Dose)
Location: Cranbury, NJ (Onsite)
Type: Contract-to-Hire
Schedule: 40 hrs/week
Shift: M-F 8am-5pm
Pay: $36-40/hour depending upon experience
Overview
Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a cGMP pharmaceutical manufacturing environment. Ideal candidates will have strong experience with solid oral dosage forms (tablets/capsules) and hands-on HPLC/UPLC analysis.
Key Responsibilities
Requirements
Keyskills
QC Chemist, Quality Control Analyst, cGMP, GMP, Pharmaceutical, Solid Dose, Solid Oral Dosage, Tablets, Capsules, HPLC, UPLC, Dissolution, Assay, Impurities, Stability Testing, Batch Release, OOS, OOT, CAPA, FDA, ICH, Empower, LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation
Benefits (via System One)
Medical, Dental, Vision, 401(k), Life Insurance, and additional voluntary benefits
System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M3-
#LI-
Ref: #558-Scientific
Location: Cranbury, NJ (Onsite)
Type: Contract-to-Hire
Schedule: 40 hrs/week
Shift: M-F 8am-5pm
Pay: $36-40/hour depending upon experience
Overview
Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a cGMP pharmaceutical manufacturing environment. Ideal candidates will have strong experience with solid oral dosage forms (tablets/capsules) and hands-on HPLC/UPLC analysis.
Key Responsibilities
- Perform batch release and stability testing for pharmaceutical products
- Conduct assay, dissolution, impurity, and related substances testing
- Operate, calibrate, and troubleshoot HPLC / UPLC systems
- Maintain GMP documentation and ensure audit readiness (ALCOA+)
- Investigate OOS / OOT results and support CAPA activities
- Manage stability programs, sample pulls, and trending analysis
- Collaborate with QA and Manufacturing to meet production timelines
Requirements
- 6-8+ years of pharmaceutical QC experience (cGMP REQUIRED)
- Strong background in solid oral dosage (tablets, capsules)
- Recent hands-on experience with HPLC / UPLC (REQUIRED)
- Experience with assay, dissolution, impurities, and stability testing
- Working knowledge of FDA, GMP, ICH guidelines
- Experience with Empower, LIMS, or similar systems
- Strong documentation, data integrity (ALCOA+), and troubleshooting skills
- Ability to work independently and in a fast-paced manufacturing setting
Keyskills
QC Chemist, Quality Control Analyst, cGMP, GMP, Pharmaceutical, Solid Dose, Solid Oral Dosage, Tablets, Capsules, HPLC, UPLC, Dissolution, Assay, Impurities, Stability Testing, Batch Release, OOS, OOT, CAPA, FDA, ICH, Empower, LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation
Benefits (via System One)
Medical, Dental, Vision, 401(k), Life Insurance, and additional voluntary benefits
System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M3-
#LI-
Ref: #558-Scientific