Analytical Chemist III - Materials & Product Validation

The Ritedose Corporation

Columbia (SC)

On-site

USD 65,000 - 90,000

Full time

8 days ago
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Job summary

The Ritedose Corporation is seeking an Analytical Services Chemist III to join our laboratory team in Columbia, SC. You will perform analytical testing across raw materials, in-process formulations, and final products within the Analytical Services Laboratory.

The role also supports method validations, transfers, and development studies. You will document data, assist with OOS investigations, and contribute to regulatory audits while maintaining instrument performance and safe, compliant

Qualifications

  • BS in Chemistry or related field with 4+ years of pharma lab experience or MS with 2+ years.
  • Expertise with standard laboratory techniques and wet chemistry tests.
  • Strong documentation skills and proficiency with office software.
  • Detail oriented with ability to work in a team environment.

Responsibilities

  • Perform chemical testing on raw materials, in-process samples, and final products.
  • Notify management of out-of-spec results and assist investigations.
  • Support method validations and transfers, including cleaning and equipment checks.
  • Maintain notebooks, batch records, and review reports as assigned.
  • Assist with regulatory audits and SOP updates as requested.
  • Ensure routine instrument maintenance and safe working environment.
  • Follow cGMP guidelines and maintain good housekeeping.

Skills

Analytical testing
Data analysis
Laboratory documentation
Team collaboration
Quality compliance

Education

BS in Chemistry or related field
MS in Chemistry or related field

Tools

HPLC
GC
ICP-MS
Malvern PSD
aPSD

Job description

The Ritedose Corporation is seeking an Analytical Services Chemist III to join our laboratory team in Columbia, SC. You will perform analytical testing across raw materials, in-process formulations, and final products within the Analytical Services Laboratory.

The role also supports method validations, transfers, and development studies. You will document data, assist with OOS investigations, and contribute to regulatory audits while maintaining instrument performance and safe, compliant

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