Analytical Scientist II: Method Development & Validation

Aveva Drug Delivery Systems Inc; Florida; On-site; USD 65,000 - 90,000; Full time

Job summary

A laboratory position at Aveva Drug Delivery Systems Inc supports development and validation of analytical methods for pharmaceutical components and drug products. You will perform HPLC/GC/UV-VIS tests, dissolution studies, and stabilitywork in a cGMP environment under supervision.

The role requires strong data interpretation, method transfer, and documentation; collaboration with project teams, and adherence to SOPs, STPs, and safety regulations.

Qualifications

• Bachelor’s degree in chemistry or related field; MS preferred.
• 2–5 years of pharmaceutical lab experience for BS holders; MS candidates may have 0–3 years.
• Knowledge of analytical methods, validation, and cGMP requirements.
• Ability to write and review SOPs, STPs, and reports.

Responsibilities

• Develop and validate analytical methods for drug products and components.
• Perform HPLC, GC, UV-VIS, dissolution, pH, and titration testing.
• Conduct stability testing and method transfer under supervision.
• Document experiments and communicate results to supervisors.

Skills

Statistics

Analytical chemistry

HPLC

Data analysis

GMP

Education

Bachelor's degree in Chemistry

Master's degree

Tools

HPLC

GC

UV-Vis

Dissolution Instruments

Job description

A laboratory position at Aveva Drug Delivery Systems Inc supports development and validation of analytical methods for pharmaceutical components and drug products. You will perform HPLC/GC/UV-VIS tests, dissolution studies, and stabilitywork in a cGMP environment under supervision.

The role requires strong data interpretation, method transfer, and documentation; collaboration with project teams, and adherence to SOPs, STPs, and safety regulations.