Job Summary This position is for 1st shift 6:00AM -2:30PM Assist in visually inspecting, labeling and packaging pharmaceutical products. Area Of Responsibility • Assists in performing visual inspections, labeling, assembling and packaging of liquids, suspensions, and lyophilized pharmaceutical and dermatological products in vials, ampoules etc. • Cleans up labeling and packaging assembly equipment and facility as needed • Comply with all policies and procedures related to personal safety and job area safety • Maintains manufacturing records and completes all required paperwork/documents to comply with Federal Regulations and FDA • Reports variance or deviations from standard procedures to department management • Stocks materials utilized by the department • Operates semi-automatic inspection machine, vial label applicator and box imprinting machines • Other duties as assigned Work Conditions: • Controlled unclassified manufacturing/production area • Warehouse office • Possible exposure to hazardous and non-hazardous chemicals Physical Requirements: • Stand, walk, sit, use hands and fingers to handle or feel, reach or push with hands and arms, talk and hear • Use of repetitive motion, unimpaired manual dexterity • Close vision, color vision, peripheral vision, depth perception, ability to focus • Correctable 20/20 vision • Ability to visually inspect small products and print • Be able to sit at workstation for up to 50 minutes at a sitting for up to 8 hours per day • Requires use of appropriate personal protective equipment (lab coat, hairnet, booties, and gloves) • Lifts up to 35lbs. Travel Estimate Up to 0% Education and Job Qualification • High School Diploma or GED required • Biotechnology certificate preferred or equivalent experience • Ability to visually inspect small print/printed labels • Ability to visually inspect liquid and lyophilized pharmaceutical products for small particles • Ability to read, write and follow written and verbal instructions/procedures in English • Ability to work independently or in a group setting Experience • Minimum 0-2 years related experience • Familiarity with, and the ability to follow established Standard Operating Procedures (SOPs), Master Batch Records, and adhere consistently to current Good Manufacturing Practices (cGMPs) • Works under direct guidance of the supervisor • Basic math skills • Basic computer skills