About the role
Job Summary This position is for 2nd shift, 1:30PM-10:00PM.
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
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Questions, answered
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