Inspection and Packaging Technician I - 2nd Shift

Sun Pharma

Billerica (MA)

Presencial

USD 22.000 - 30.000

Jornada completa

hace 38 horas
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Descripción de la vacante

Sun Pharmaceutical Industries, Inc (USA) is seeking an Inspection and Packaging Technician I for the 2nd shift (1:30PM - 10:00PM). The role involves visually inspecting, labeling and packaging pharmaceutical products, ensuring compliance with FDA regulations and safety procedures.

The position requires a high school diploma or GED, with biotechnology certification preferred or equivalent experience. Candidates should be able to read and follow written and verbal instructions in English and work

Formación

  • High School Diploma or GED required.
  • Biotechnology certificate preferred or equivalent experience.
  • Ability to read, write and follow written and verbal instructions/procedures in English.
  • Ability to work independently or in a group setting.

Responsabilidades

  • Visually inspect, label and package liquids, suspensions, and lyophilized pharmaceutical and dermatological products in various containers.
  • Clean up labeling and packaging assembly equipment and facility as needed.
  • Comply with all policies and procedures related to personal safety and job area safety.
  • Maintain manufacturing records and complete all required paperwork/documents to comply with Federal Regulations and FDA.
  • Report variance or deviations from standard procedures to department management.
  • Stock materials utilized by the department.
  • Operate semi-automatic inspection machine, vial label applicator and box imprinting machines.
  • Other duties as assigned.

Educación

High School Diploma or GED
Biotechnology certificate

Descripción del empleo

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Title: Inspection and Packaging Technician I - 2nd Shift

Date: Oct 29, 2026

Company: Sun Pharmaceutical Industries, Inc (USA)

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
  • 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.

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
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