A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
Tamarac, FL Job Details $50,000 - $80,000 a year 4 hours ago Qualifications Laboratory quality control
Full Job Description Job Summary:
Performs analytical testing of raw materials, and components. Job Responsabilities Performs testing of analytical assays, including
HPLC, GC, UV
testing for raw materials. Perform raw materials and components ID methods. Reviews laboratory data as assigned by Supervisor Perform testing following compendial methods (USP, EP, JP) Maintains proficiency with data acquisition systems Calibrates analytical instrumentation by standard protocol Revises STPs and SOPs and Specifications Assists the supervisor in training new chemists Perform method transfer or method verifications. Performs IQ/OQ of analytical instrumentation Troubleshoots instrumentation with guidance of Supervisor Other general QC laboratory responsibilities as assigned Support housekeeping and maintenance activities 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 Performs all work in support of our
Values:
Collaboration, Courage, Perseverance, and Passion All other relevant duties as assigned Education o Bachelor's degree (B.S.) in chemistry or related field or; o Master's degree (M.S.) in chemistry or related field Knowledge, Skills and Abilities o Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of algebra. Ability to apply concepts such as fractions, percentages, ratios, linear regression, and proportions to practical situations. o 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. o Experience in the testing of raw materials. o Working knowledge of GC, HPLC, Karl Fisher, FTIR, UV spectroscopic methods, and compendial methods. o Ability to read analyze, and interpret common scientific and technical journals, specifications, standard operating procedures, and standard testing procedures. o Knowledge FDA, cGMPs, and SOPs Experience o A minimum of two to five (2-5) years of QC laboratory experience (Bachelor's degree) o A minimum of two (2) years of QC laboratory experience (Master's degree)
