Job Summary Second shift 1:30PM - 10PM

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