Associate Scientist II

3/29/22

Wilmington, NC

1634

The Associate Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile.

Essential Functions

  • Performs laboratory work related to analytical testing and method development in support of contract pharmaceuticals.
  • Evaluates and interprets generated data.
  • Analyzes information for technical correctness and accuracy.
  • Understands the theoretical basis of the methods/experiments.
  • Works on problems of diverse scope in which analysis of data requires evaluation of identifiable factors.
  • Writes standard operating procedures (SOPs), test procedures, specifications and summary reports.
  • Maintains working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
  • Maintains a safe, clean, and organized work environment free of safety hazards.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.

Education and Experience

  • Bachelor’s degree in Pharmaceutical Sciences, Chemistry or equivalent required.
  • Prior laboratory experience or work experience in Pharmaceutical, CDMO, or cGMP preferred.

Travel Requirements

  • Up to 5% domestic Travel.
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