QC Analyst III

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

Job Details

Job Location: Miramar, FL 33025
Position Type: Full Time
Job Shift: Any

Responsibilities

• Supports release and stability testing for raw materials, components, standards, intermediate/finished products
• Prepares and executes verification protocols for in-house/compendia test methods
• Executes technology transfer protocols and assists in evaluations
• Analytical support to ARD for qualification/validation of test methods
• Reviews laboratory work and approves data packages as designated by the Supervisor
• Maintains a heighten proficiency with data acquisition systems;
• Execute methods for calibration of analytical instrumentation
• Writes and reviews STPs, SOPs, Specifications and technical reports
• Trains analysts on methods and instrumentation
• Independently troubleshoots instrumentation
• Maintains QC compliance systems with guidance of Supervisor
• Coordinates testing schedules and monitors status of sample testing as assigned by the Supervisor
• Works as a member of a team to achieve all outcomes
• Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements
• All other relevant duties as assigned

Qualifications

• Ability to apply advances mathematical concepts such as exponents, logarithms, quadratic equations, linear regression, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, and correlation techniques.
• Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
• Ability to read, analyze, and interpret common scientific and technical journals, specifications, standard operating procedures, and standard testing procedures. Ability to write presentations and articles that conform to prescribed style and form. Ability to effectively present information to middle management.
• Knowledge FDA, cGMPs, and SOPs

Experience

• A minimum of five to seven (5-7) years of QC laboratory experience (Bachelor’s degree)
• A minimum of two to five (2-5) years of QC laboratory experience (Master’s degree)
• A minimum of two (2) years lab experience (Ph.D. degree)