Analytical Testing Scientist II - HPLC, GC & Method Dev

Alcami-5; Durham (NC); On-site; USD 65,000 - 90,000; Full time

Job summary

Alcami is seeking a Scientist II to drive analytical testing in a fast-paced pharmaceutical development environment. You will perform routine and non-routine analyses using HPLC, dissolution, GC, UV, and KF, and contribute to method development or validation projects in support of product development or manufacturing.

On-site, 1st shift, with responsibilities including data evaluation, procedure writing, and safe handling of hazardous materials, while ensuring cGMP compliance and proper

Qualifications

• Master’s degree in Chemistry or similar field with 0+ years related experience.
• Bachelor’s degree in Chemistry or similar field with 4+ years related experience.
• Associate’s degree in Chemistry or related field with 10+ years related experience.

Responsibilities

• Develops analytical methodology for analysis via HPLC, dissolution, GC, UV, and/or KF.
• Performs one or more of the following techniques: residual solvents, assays, dissolution, impurities, moisture content, identification.
• Evaluates and interprets generated data.
• Writes test procedures, protocols, and reports.
• Maintains a safe, clean, and organized work environment; handles hazardous materials.

Skills

Analytical thinking

Verbal and written communication

Detail-oriented

Troubleshooting

Laboratory safety

cGMP knowledge

Microsoft Office

Education

Master’s degree in Chemistry or related field

Bachelor’s degree in Chemistry or related field

Associate’s degree in Chemistry or related field

Tools

Empower3

ProCal

Master Control

ELN

Job description

Alcami is seeking a Scientist II to drive analytical testing in a fast-paced pharmaceutical development environment. You will perform routine and non-routine analyses using HPLC, dissolution, GC, UV, and KF, and contribute to method development or validation projects in support of product development or manufacturing.

On-site, 1st shift, with responsibilities including data evaluation, procedure writing, and safe handling of hazardous materials, while ensuring cGMP compliance and proper