Lead QC Analyst - Method Validation & Tech Transfer

Aveva Drug Delivery Systems; Town of Florida (NY); On-site; USD 60,000 - 80,000; Full time

Job summary

Aveva Drug Delivery Systems is seeking a qualified professional for a QC laboratory role in Miramar, FL. Candidates should have strong analytical skills and extensive QC laboratory experience. Responsibilities include supporting release and stability testing, preparing verification protocols, and ensuring compliance with regulations.

The successful candidate must possess a Bachelor's degree and 5-7 years of QC experience, along with a solid understanding of FDA and cGMP guidelines.

Qualifications

• Ability to apply advanced mathematical concepts such as exponents and logarithms.
• Ability to define problems, collect data, and draw valid conclusions.
• Ability to read, analyze, and interpret scientific and technical journals.
• Knowledge of FDA regulations, cGMPs, and SOPs.

Responsibilities

• Supports release and stability testing for raw materials.
• Prepares and executes verification protocols for testing methods.
• Executes technology transfer protocols and assists in evaluations.
• Reviews laboratory work and approves data packages as designated.
• Trains analysts on methods and instrumentation.

Job description

Aveva Drug Delivery Systems is seeking a qualified professional for a QC laboratory role in Miramar, FL. Candidates should have strong analytical skills and extensive QC laboratory experience. Responsibilities include supporting release and stability testing, preparing verification protocols, and ensuring compliance with regulations.

The successful candidate must possess a Bachelor's degree and 5-7 years of QC experience, along with a solid understanding of FDA and cGMP guidelines.