QC Chemist

Joulé

Cranbury, NJ

JOB DETAILS
SALARY
$36–$40 Per Hour
SKILLS
Analysis Skills, Assays, Biotech and Pharmaceutical, Capsules, Chemistry, Consulting, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Data Quality, Documentation, Dosage Forms, Drug Manufacturing, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), ICH Regulations, Identify Issues, Laboratory Information Management System (LIMS), Manufacturing, Outsourcing, Product Testing, Project/Program Management, Quality Assurance, Quality Control, Service Delivery, Stability Analysis, Testing, Time Management, Trend Analysis
LOCATION
Cranbury, NJ
POSTED
2 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

  • 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.

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Ref: #558-Scientific


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/