Somerset, NJ · On-site
The Quality Control Chemist-I is responsible for conducting routine testing and analysis of raw materials, in-process materials, and finished product samples using various analytical methodologies to ...
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Somerset, NJ · On-site
The Quality Control Chemist-I is responsible for conducting routine testing and analysis of raw materials, in-process materials, and finished product samples using various analytical methodologies to ...
For more details, please visit : www.piramalpharmasolutions.com Job Title Quality Control Chemist I Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in ...
For more details, please visit : www.piramalpharmasolutions.com Job Title Quality Control Chemist I Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in ...
Riverview, MI · On-site
For more details, please visit : www.piramalpharmasolutions.com Job Title Quality Control Chemist I Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in ...
New
Riverview, MI · On-site
For more details, please visit : www.piramalpharmasolutions.com Job Title Quality Control Chemist I Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in ...
New
San Diego, CA · On-site
$70K - $72K/yr
QC Chemist I About Site Catalent's San Diego, CA site is an early-phase development facility supporting small-molecule and peptide programs from preformulation through cGMP clinical manufacturing for ...
San Diego, CA · On-site
$70K - $72K/yr
QC Chemist I About Site Catalent's San Diego, CA site is an early-phase development facility supporting small-molecule and peptide programs from preformulation through cGMP clinical manufacturing for ...
San Diego, CA · On-site
$70K - $72K/yr
QC Chemist I About Site Catalent's San Diego, CA site is an earlyphase development facility supporting smallmolecule and peptide programs from preformulation through cGMP clinical manufacturing for ...
San Diego, CA · On-site
$70K - $72K/yr
QC Chemist I About Site Catalent's San Diego, CA site is an earlyphase development facility supporting smallmolecule and peptide programs from preformulation through cGMP clinical manufacturing for ...
Fort Worth, TX · On-site
Summary / Objective The primary function of a QC Chemist I is to perform qualitative and quantitative chemical and physical analyses at a high level in support of one of the following areas:
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Fort Worth, TX · On-site
Summary / Objective The primary function of a QC Chemist I is to perform qualitative and quantitative chemical and physical analyses at a high level in support of one of the following areas:
Fort Worth, TX · On-site
Summary / Objective The primary function of a QC Chemist I is to perform qualitative and quantitative chemical and physical analyses at a high level in support of one of the following areas:
Fort Worth, TX · On-site
Summary / Objective The primary function of a QC Chemist I is to perform qualitative and quantitative chemical and physical analyses at a high level in support of one of the following areas:
Job Overview The Chemist I in Quality Control is responsible for performing a variety of chemical analyses to ensure the release of raw materials, intermediates, and finished products. The role ...
Job Overview The Chemist I in Quality Control is responsible for performing a variety of chemical analyses to ensure the release of raw materials, intermediates, and finished products. The role ...
The Chemist I in Quality Control is responsible for performing a variety of chemical analyses to ensure the release of raw materials, intermediates, and finished products. The role requires adherence ...
The Chemist I in Quality Control is responsible for performing a variety of chemical analyses to ensure the release of raw materials, intermediates, and finished products. The role requires adherence ...
Job Overview The Chemist I in Quality Control is responsible for performing a variety of chemical analyses to ensure the release of raw materials, intermediates, and finished products. The role ...
Job Overview The Chemist I in Quality Control is responsible for performing a variety of chemical analyses to ensure the release of raw materials, intermediates, and finished products. The role ...
Central Islip, NY · On-site
$65K - $90K/wk
Job Title: QC Chemist I Location: Central Islip, NY (Onsite) Job Type: Full-Time | Permanent Shift: 8:30 AM - 5:00 PM (may vary) Industry: Pharmaceutical Experience Required: 2 to 15 years ...
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Central Islip, NY · On-site
$65K - $90K/wk
Job Title: QC Chemist I Location: Central Islip, NY (Onsite) Job Type: Full-Time | Permanent Shift: 8:30 AM - 5:00 PM (may vary) Industry: Pharmaceutical Experience Required: 2 to 15 years ...
Rocky Mount, NC · On-site
Prepare periodic and special reports concerning quality control and results of laboratory tests ... Perform mathematical calculations applicable to chemistry testing. Work cooperatively with others.
Rocky Mount, NC · On-site
Prepare periodic and special reports concerning quality control and results of laboratory tests ... Perform mathematical calculations applicable to chemistry testing. Work cooperatively with others.
Arlington Heights, IL · On-site
$52K - $78K/yr
Experience in a FDA regulated QC environment. * Background in Math or Chemistry. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with ...
Arlington Heights, IL · On-site
$52K - $78K/yr
Experience in a FDA regulated QC environment. * Background in Math or Chemistry. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with ...
Arlington Heights, IL · On-site
$52K - $78K/yr
Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment * Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act ...
Arlington Heights, IL · On-site
$52K - $78K/yr
Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment * Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act ...
Arlington Heights, IL · On-site
$52K - $78K/yr
Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment * Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act ...
Arlington Heights, IL · On-site
$52K - $78K/yr
Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment * Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act ...
San Diego, CA · On-site
$73K - $116K/yr
The Quality Control Chemist I will support raw material, in-process material, and finish product lot release, stability studies, engineering evaluations, and anyrelevant investigation by performing ...
New
San Diego, CA · On-site
$73K - $116K/yr
The Quality Control Chemist I will support raw material, in-process material, and finish product lot release, stability studies, engineering evaluations, and anyrelevant investigation by performing ...
New
Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties: * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...
Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties: * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...
San Diego, CA · On-site
$73K - $116K/yr
The Quality Control Chemist I will support raw material, in-process material, and finish product lot release, stability studies, engineering evaluations, and anyrelevant investigation by performing ...
New
San Diego, CA · On-site
$73K - $116K/yr
The Quality Control Chemist I will support raw material, in-process material, and finish product lot release, stability studies, engineering evaluations, and anyrelevant investigation by performing ...
New
Ann Arbor, MI · On-site
Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...
Ann Arbor, MI · On-site
Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...
Ann Arbor, MI · On-site
Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties: * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...
Ann Arbor, MI · On-site
Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties: * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...
$17.79 - $20.30
4% of jobs
$20.30 - $22.81
4% of jobs
$22.81 - $25.33
14% of jobs
$25.66 is the 25th percentile. Wages below this are outliers.
$25.33 - $27.84
16% of jobs
The median wage is $29.24 / hr.
$27.84 - $30.35
20% of jobs
$30.35 - $32.87
13% of jobs
$34.12 is the 75th percentile. Wages above this are outliers.
$32.87 - $35.38
7% of jobs
$35.38 - $37.89
4% of jobs
$37.89 - $40.41
7% of jobs
$40.41 - $42.92
7% of jobs
$42.92 - $45.43
4% of jobs
$17
$31
$45
| Aspect | Quality Control Chemist I | Quality Control Analyst |
|---|---|---|
| Credentials | Bachelor's in Chemistry or related field; may require certifications | Bachelor's in Chemistry, Biochemistry, or related; similar certifications often required |
| Work Environment | Laboratories, manufacturing facilities, quality testing labs | Laboratories, quality assurance departments, manufacturing sites |
| Employer & Industry Usage | Pharmaceutical, biotech, food, and beverage industries | Pharmaceutical, biotech, cosmetics, and food industries |
| Common Search & Comparison | Yes | Yes |
The main difference between a Quality Control Chemist I and a Quality Control Analyst lies in job titles used across industries. Both roles typically require similar educational backgrounds and certifications, and they work in comparable environments such as laboratories and manufacturing facilities. While the titles may vary, their responsibilities often overlap in testing and ensuring product quality within pharmaceutical, biotech, and food sectors.
Cities with the most Quality Control Chemist I job openings:
States with the most job openings for Quality Control Chemist I jobs include:
For Quality Control Chemist I jobs, the most frequently searched job titles are:
Somerset, NJ • On-site
Other
Re-posted 20 hours ago
Position Description: Position Summary:The Quality Control Chemist-I is responsible for conducting routine testing and analysis of raw materials, in-process materials, and finished product samples using various analytical methodologies to ensure the quality of dietary supplements and OTC products. This role includes reviewing and maintaining Standard Operating Procedures (SOPs), Testing Procedures, calibrations, and other controlled documents to ensure compliance with regulatory standards and internal procedures. Additionally, the Chemist-I will assist in quality control stability testing and contribute to maintaining accurate records and documentation.DUTIES AND RESPONSIBILITIES:Ensure all work is performed in compliance with cGMP, GLP, compendia standards, and internal procedures. Conduct wet chemistry and analytical testing on raw materials, finished products, in-process samples, stability, and packaged products according to Testing Procedures.Assist in quality control stability testing, prepare, and maintain stability records and summaries.Operate, maintain, and troubleshoot analytical instruments, including pH meter, FTIR, TOC, UV, and others as necessary.Maintain accurate records of all analyses, ensuring contemporaneous documentation and adherence to company standards.Perform laboratory analysis right the first time and ensure all results are properly documented.Conduct laboratory investigations under the guidance of laboratory management.Work effectively under the direction of supervisors and/or manager, and perform additional duties as required.QUALIFICATION AND EXPERIENCE:Bachelor’s degree in chemistry, Biochemistry, Pharmaceutical Sciences, or related field with 0 - 3 years of relevant experience in a quality control setting; or an equivalent combination of education and experience.Basic understanding of Current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and quality control principles in the pharmaceutical industry.Math skills commensurate with a scientific background are required.Ability to communicate test results and observations clearly, both verbally and in writing. Ability to follow written instructions and solve basic analytical problems using standard procedures.
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Aspire Pharmaceuticals was established more than a decade ago with the sole purpose of bringing innovation and excellence to the encapsulation category. Billions of softgel later, the business has grown exponentially with a customer roster that represents some of the most influential players in the nutritional supplement and OTC industries. Aspire’s passion in the encapsulation space has moved beyond softgel to include liquid capsules and liposome technology, all of which allow us to offer a larger variety of solutions to customers. As a leader in the development AND manufacturing of softgel and liquid capsule supplements and OTC products, we take that role with pride. Our promise to you is that we will never stop asking the question: How can we do it better? We’ve been asking that very same question each year since our inception.
Pharmaceutical and medicine manufacturing
51 - 200 Employees
Somerset, NJ, US
2009
