Senior Quality Control Associate

Primary Duties and Responsibilities

Support Quality Control departments in duties including but not limited to :

• Conduct Analysis in compliance with cGMP requirements, compendia standards, and internal procedures. Performs Dietary supplement analysis to support manufacturing which includes instrumental and physical testing.
• Maintain accurate record of analysis and perform documentation to company standards. Perform laboratory analysis right the first time and document the results contemporaneously.
• Notify the manager immediately of nonconforming data or unexpected occurrences.
• Reviews and analyzes the stability samples and associated analytical data, prepares or assists in preparing Stability Summary Reports.
• Reviews / Checks of analytical data by following test methods / SOPs.
• Conducts laboratory investigation under the supervision of laboratory management.
• Organize work schedule to complete assigned tasks efficiently and on schedule.
• Ensures the laboratory is kept in a safe working environment and compliance with OSHA and other laboratory safety standards.
• Ensure and maintain retained samples.
• Pulling of samples.
• Organization of retaining cages.
• Oversight and Inspect production lines throughout the production run.
• Helping to eliminate errors / Line Clearance
• Test and monitor the facility's environment for microbial contaminants.
• Water system, Air monitoring, Drains, Hoses and Sinks,
• Inspect, test, and release cleaned equipment
• Working closely with sanitation personnel
• Maintain the trending of data / results generated from the environmental monitoring and cleaning equipment verifications.
• Maintain laboratory equipment and assist in ordering laboratory supplies.
• Reagents, Microbiology media, Lab utensils, etc.
• Testing of raw materials, components, finished products, and stability.
• Send appropriate samples to 3rd party laboratories.
• Ensure lab testing is being conducted properly.
• Statistical sampling plans.
• Update laboratory reagents / chemicals list as needed.
• Write and revise Standard Operating Procedures, testing specifications, protocols, and reports as needed.
• Record all data and results in specified forms, record books or logbooks with accuracy.
• Assist with filing documents.
• Assist with cleaning / method validation studies.
• Locate opportunities for continuous improvement.
• Other duties as assigned by Quality Management.
• Travel required : approximately 10% between different locations

Qualifications

Qualifications include :