Senior Analytical Chemist - HPLC, cGMP & Transfers

Automatic Data Processing, Inc.

Mount Laurel Township (NJ)

On-site

USD 90,000 - 140,000

Full time

8 days ago

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Job summary

Stokes Healthcare in Mount Laurel, NJ, is seeking a seasoned analytical chemist to perform and supervise cGMP testing of finished products, raw materials, and stability samples. You will review data, lead investigations, and contribute to SOPs and method transfers.

The ideal candidate has a chemistry degree and 10+ years of pharmaceutical analytical experience, with hands-on HPLC/UPLC and Empower 3 expertise, and can work both independently and as part of a team.

Qualifications

  • Bachelor’s Degree in chemistry or relevant field.
  • Minimum 10 years of experience in pharmaceutical analytical testing.
  • Experience with HPLC/UPLC analysis, preferably Empower 3.
  • Familiar with GMPs, FDA, ICH and OSHA requirements.
  • Experience using MS Word, Excel, and/or relevant applications.
  • Must be capable of wearing protective wear as required by regulations.
  • Must be able to work with chemicals used in sample analysis following safety precautions.
  • Ability to work independently and as part of a team.

Responsibilities

  • Independently performs analytical testing of Finished Product, R&D Materials, Stability Samples and Raw Materials.
  • Ensure testing is performed in accordance with cGMP, USP, ICH, FDA and company standards.
  • Review and approve analytical testing data; lead investigations.
  • Authors/revises SOPs, protocols and data reports; tracks and trends data.
  • Performs method transfer and leads qualification and calibration of equipment.

Skills

Analytical testing
GxP compliance
Data review
Problem solving

Education

Bachelor’s Degree in chemistry

Tools

Empower 3
HPLC/UPLC equipment
Karl Fischer
pH meter
Analytical balance
Centrifuge

Job description

Stokes Healthcare in Mount Laurel, NJ, is seeking a seasoned analytical chemist to perform and supervise cGMP testing of finished products, raw materials, and stability samples. You will review data, lead investigations, and contribute to SOPs and method transfers.

The ideal candidate has a chemistry degree and 10+ years of pharmaceutical analytical experience, with hands-on HPLC/UPLC and Empower 3 expertise, and can work both independently and as part of a team.

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