Scientist III, Analytical Development Laboratory

$85,500 - $111,250/Yr

The Us Pharmacopeial Convention - Rockville, MD

Full-time - Mid Level

Rockville, MD

1,001-5,000 employees

About the position

The Scientist III position at USP is a non-supervisory, technical role within the Analytical Development Laboratory (ADL). The primary responsibility is to work on projects related to the research, evaluation, development, and validation of analytical procedures that support USP's products and services, focusing on the identity, strength, and purity of small molecule and biologic drug substances. This hands-on role requires expertise in analytical techniques, particularly chromatography, and involves significant laboratory work.

Responsibilities

• Evaluate, develop, and validate chromatographic procedures for analysis of drug substances.
• Plan and implement experiments, providing input and drawing conclusions with the project team.
• Assess submitted procedures based on method verification and support the review of final drafts.
• Apply personal experience and academic training to address technical problems.
• Collaborate in a team setting to achieve project goals.
• Demonstrate a strong desire for continuous learning and seek growth opportunities.
• Participate and/or present at scientific meetings and share technical expertise with laboratory staff.
• Recommend and implement creative approaches to improve laboratory operations.

Requirements

• Bachelor's degree in a scientific field with seven years of experience, or
• Master's degree in a scientific field with five years of experience, or
• Ph.D. in a scientific field.
• Hands-on experience with separation analyses such as HPLC and GC.
• Understanding of general chemistry principles and techniques.

Nice-to-haves

• Knowledge of small molecule/biologic drug substance analysis by spectroscopic techniques (IR, UV-Vis).
• Experience with LC-MS and/or GC-MS.
• Experience in a fast-paced environment with multi-layered priorities.
• Ability to manage multiple tasks concurrently.
• Experience in the compendial, pharmaceutical, chemical, or biotechnology industry.
• Experience in GLP or ISO-17025 regulated laboratories.
• Familiarity with Empower chromatography software and Electronic Laboratory Notebook Software.

Benefits

• Company-paid time off
• Comprehensive healthcare options
• Retirement savings plans