Analytical Scientist - Associate (Pharma Chemistry)

Alcami Corporation

St. Louis (MO)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Job summary

Alcami Corporation in St. Louis, MO, is seeking an Associate Scientist to perform analytical testing in support of pharmaceutical product development and manufacturing. The role uses UV-Vis, FTIR, HPLC, GC, titration, and/or AA methodologies.

The successful candidate will work 1st shift, Monday–Friday, on-site, with responsibilities including technique execution, instrument maintenance, SOP compliance, and collaboration within a GMP-regulated setting.

Qualifications

  • Excellent verbal and written communication and documentation skills.
  • Excellent detail orientation and organizational skills.
  • Excellent problem-solving and basic trouble-shooting ability.
  • Basic knowledge of Laboratory equipment and safety.
  • Basic knowledge of Laboratory Documentation is required.
  • Working knowledge of cGMP in a pharmaceutical or regulated environment preferred.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.

Responsibilities

  • Performs one or more analytical techniques (residual solvents, assays, dissolution, impurities, moisture content, identification).
  • Maintains knowledge of routine instrumentation and methodologies.
  • Follows SOPs and supervisor instructions; ensures accuracy of information.
  • Analyzes information for technical correctness and accuracy.
  • Complies with GMPs and GMP review processes; flags anomalies to supervisor.
  • Maintains safe, clean, organized work environment; suggests safety/quality improvements.
  • Meets training requirements and supports team culture and mentorship.

Skills

Communication
Detail-oriented
Problem solving
Lab equipment knowledge
Laboratory documentation
cGMP knowledge
MS Office
SOP adherence

Education

Bachelor's degree in chemistry or related field

Job description

Alcami Corporation in St. Louis, MO, is seeking an Associate Scientist to perform analytical testing in support of pharmaceutical product development and manufacturing. The role uses UV-Vis, FTIR, HPLC, GC, titration, and/or AA methodologies.

The successful candidate will work 1st shift, Monday–Friday, on-site, with responsibilities including technique execution, instrument maintenance, SOP compliance, and collaboration within a GMP-regulated setting.

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