Associate Scientist/chemist/QC/

Description

• Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.
• Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.
• Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.
• Analyze and interpret results in both written and oral formats.
• Review notebooks promptly and ensure compliance with SOPs.
• Evaluate test results and determine the acceptability of samples based on the results.
• Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.
• Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.

Requirements

• Working knowledge of instrumentation software used in laboratories.
• Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.
• Ability to analyze and interpret complex data.
• Familiarity with FDA and GMP regulations.
• Require Bachelors in Chemistry, No Ph.D
• Proficiency in HPLC, UPLC, and UV-Vis techniques.

Benefits

• Employee Assistance Program
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Critical Illness, Accident, and Hospital
• Time Off/Leave (PTO, Vacation or Sick Leave)
• Transportation benefits
• Medical, dental & vision
• Health Spending Account (HSA)
• Short and long-term disability
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)

Training + Development

Interview process

Visa Sponsorship

Security clearance