Cranbury, NJ · On-site
$36 - $40/hr
Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...
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Cranbury, NJ · On-site
$36 - $40/hr
Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...
Cranbury, NJ · On-site
$36 - $40/hr
Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...
Quick apply
Cranbury, NJ · On-site
$36 - $40/hr
Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...
$65K - $105K/yr
What You'll Do Analytical Testing & Expertise Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) Evaluate critical ...
$65K - $105K/yr
What You'll Do Analytical Testing & Expertise Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) Evaluate critical ...
Parsippany, NJ · On-site
Partner cross-functionally with Pharmaceutical Development, Technical Operations, QA, and CMC ... Lead or support QC-related projects and propose improvements using risk-based approaches.
Parsippany, NJ · On-site
Partner cross-functionally with Pharmaceutical Development, Technical Operations, QA, and CMC ... Lead or support QC-related projects and propose improvements using risk-based approaches.
Partner cross-functionally with Pharmaceutical Development, Technical Operations, QA, and CMC ... Lead or support QC-related projects and propose improvements using risk-based approaches.
Partner cross-functionally with Pharmaceutical Development, Technical Operations, QA, and CMC ... Lead or support QC-related projects and propose improvements using risk-based approaches.
Seminole, FL · On-site
$85K - $87K/yr
Minimum -5 years of relevant pharmaceutical QC experience, with at least 3 or more years in a direct supervisory or leadership role. * Regulatory Knowledge: Deep understanding of cGMP, FDA ...
Seminole, FL · On-site
$85K - $87K/yr
Minimum -5 years of relevant pharmaceutical QC experience, with at least 3 or more years in a direct supervisory or leadership role. * Regulatory Knowledge: Deep understanding of cGMP, FDA ...
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Sylmar, CA · On-site
$25 - $30/hr
A pharmaceutical Quality Assurance (QA) professional ensures that drug products are safe, effective ... Document Control: Author, review, and manage Standard Operating Procedures (SOPs), protocols, and ...
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Sylmar, CA · On-site
$25 - $30/hr
A pharmaceutical Quality Assurance (QA) professional ensures that drug products are safe, effective ... Document Control: Author, review, and manage Standard Operating Procedures (SOPs), protocols, and ...
Fremont, CA · On-site
$41/hr
Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...
Fremont, CA · On-site
$41/hr
Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...
Our client, a world-leading Pharmaceutical Company in Pearl River, NY is currently looking for an QC Chemist to join their expanding team. Job Title: QC Chemist / Pharma Industry Duration: 6 months ...
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Our client, a world-leading Pharmaceutical Company in Pearl River, NY is currently looking for an QC Chemist to join their expanding team. Job Title: QC Chemist / Pharma Industry Duration: 6 months ...
Sellersville, PA · On-site
$23.25 - $31.25/hr
Experience in pharmaceutical, biotechnology, or other regulated laboratory environments ... Quality Control laboratory environment supporting pharmaceutical manufacturing operations.
Sellersville, PA · On-site
$23.25 - $31.25/hr
Experience in pharmaceutical, biotechnology, or other regulated laboratory environments ... Quality Control laboratory environment supporting pharmaceutical manufacturing operations.
Sellersville, PA · On-site
$23.25 - $31.25/hr
Experience in pharmaceutical, biotechnology, or other regulated laboratory environments ... Quality Control laboratory environment supporting pharmaceutical manufacturing operations.
Sellersville, PA · On-site
$23.25 - $31.25/hr
Experience in pharmaceutical, biotechnology, or other regulated laboratory environments ... Quality Control laboratory environment supporting pharmaceutical manufacturing operations.
QC Chemistry Lead At Guerbet, we build lasting relationships so that to enable people to live ... We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals ...
QC Chemistry Lead At Guerbet, we build lasting relationships so that to enable people to live ... We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals ...
Raleigh, IL · On-site
QC Chemistry Lead At Guerbet, we build lasting relationships so that to enable people to live ... We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals ...
Raleigh, IL · On-site
QC Chemistry Lead At Guerbet, we build lasting relationships so that to enable people to live ... We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals ...
Rensselaer, NY · On-site
$91K/yr
Senior Quality Control Analyst (Pharmaceuticals) Role Overview We are seeking a highly skilled Senior Quality Control Analyst to join our laboratory operations team. In this role, you will perform ...
Rensselaer, NY · On-site
$91K/yr
Senior Quality Control Analyst (Pharmaceuticals) Role Overview We are seeking a highly skilled Senior Quality Control Analyst to join our laboratory operations team. In this role, you will perform ...
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Newtown, PA · On-site
$90K - $105K/yr
S.-based generic and specialty pharmaceutical manufacturer committed to developing and producing ... What You'll Do The QC Chemist III serves as a senior analytical scientist and technical resource ...
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Newtown, PA · On-site
$90K - $105K/yr
S.-based generic and specialty pharmaceutical manufacturer committed to developing and producing ... What You'll Do The QC Chemist III serves as a senior analytical scientist and technical resource ...
Menlo Park, CA · On-site
$160K - $195K/yr
Advanced degree preferred. * 10+ years of progressive experience in pharmaceutical QC under GMP regulations, with 5+ years in a leadership or managerial role. * Demonstrated experience managing QC ...
Menlo Park, CA · On-site
$160K - $195K/yr
Advanced degree preferred. * 10+ years of progressive experience in pharmaceutical QC under GMP regulations, with 5+ years in a leadership or managerial role. * Demonstrated experience managing QC ...
Waltham, MA · On-site
Participates in Pharmaceutical Quality leadership team activities, contributing to functional goals, priorities, and budgets * Leads and develops QC personnel, including oversight of training ...
Waltham, MA · On-site
Participates in Pharmaceutical Quality leadership team activities, contributing to functional goals, priorities, and budgets * Leads and develops QC personnel, including oversight of training ...
Washington, DC · On-site
$13 - $15/hr
Health insurance The full-time Pharmaceutical Quality Control Associate is responsible for completing the necessary quality checks that include but are not limited to ensuring the accuracy of ...
Washington, DC · On-site
$13 - $15/hr
Health insurance The full-time Pharmaceutical Quality Control Associate is responsible for completing the necessary quality checks that include but are not limited to ensuring the accuracy of ...
Bloomsbury, NJ · On-site
$113K - $177K/yr
Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences, or related field required * Master's or PhD preferred * 10+ years of experience in pharmaceutical QC, QA, or compliance within a ...
Bloomsbury, NJ · On-site
$113K - $177K/yr
Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences, or related field required * Master's or PhD preferred * 10+ years of experience in pharmaceutical QC, QA, or compliance within a ...
Fremont, CA · On-site
$41/hr
Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...
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Fremont, CA · On-site
$41/hr
Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...
| Aspect | Internship Pharmaceutical Quality Control | Pharmaceutical Quality Control Analyst |
|---|---|---|
| Qualifications | Enrolled in or recent graduate of related degree | Bachelor's degree in pharmacy, chemistry, or related field |
| Work Environment | Training-focused, supervised lab setting | Full-time professional lab environment |
| Responsibilities | Assisting with tests, learning procedures | Performing quality tests, data analysis |
Internship Pharmaceutical Quality Control roles are entry-level positions designed for students or recent graduates to gain industry experience. In contrast, Pharmaceutical Quality Control Analysts are full-time professionals responsible for executing quality tests and ensuring product compliance. The internship provides foundational exposure, while the analyst role involves independent work and responsibility.
$36 - $40/hr
Contractor
Medical, Dental, Vision, Life, Retirement
Re-posted 22 days ago
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
