Chemist

Chemist


Job ID: 10218754

Norwood, NJ, US

Scientific

Bachelors Degree

Full Time, Temporary

$37.00

Experienced (Non-Manager)

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Norwood, NJ, US

$37.00

Experienced (Non-Manager)

Full Time, Temporary

Biotechnology/Pharmaceuticals

On-site

Scientific

Bachelors Degree

First Shift (Day)

Job details

Quality Control Chemist- Northvale, NJ
The Quality Control Chemist will conduct release and stability testing for pharmaceutical products with a specific focus on LC and GC chromatographic analyses, dissolution testing, and Karl Fischer (KF) water content testing. This role involves performing analytical testing to ensure the quality, safety, and performance of solid oral dosage pharmaceutical products while maintaining compliance with laboratory safety and regulatory requirements.
Key Responsibilities

  1. Sample Preparation: Prepare solid dosage samples for analysis by accurately weighing, blending, and homogenizing materials to ensure representative samples for testing.

  2. Dissolution Testing: Conduct dissolution testing of solid oral drug products using USP Apparatus I and USP Apparatus II.

  3. Chromatographic Analysis: Perform HPLC and GC analyses for quantitative and qualitative evaluation of pharmaceutical components, including potency, purity, impurities, and dissolution samples.

  4. KF Testing: Conduct water content testing using Karl Fischer titration techniques.

  5. Instrument Maintenance: Ensure analytical instrumentation is properly operated, calibrated, and maintained according to laboratory procedures.

  6. Quality Compliance: Perform all laboratory activities in compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and established Standard Operating Procedures (SOPs).

  7. Documentation: Maintain accurate, complete, and contemporaneous laboratory records in notebooks and electronic systems, ensuring data integrity and compliance with regulatory standards.

Minimum Qualifications

  • Bachelor’s degree in Chemistry or related scientific discipline with at least two (2) years of pharmaceutical industry experience.

  • Hands-on experience with HPLC, GC, dissolution testing, and KF titration.

  • High attention to detail with a strong commitment to data integrity and quality compliance.

10218754

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