TEMP Inspection Labeling and Packaging Tech I (2nd shift) 1:30PM-10PM

Sun Pharmaceutical Industries, Inc.; Billerica, Northern (MA, KY); On-site; USD 36,000 - 48,000; Full time

Job summary

Sun Pharmaceutical Industries, Inc. seeks a TEMP Inspection Labeling and Packaging Tech I for the second shift (1:30PM–10PM) to assist in visually inspecting, labeling and packaging pharmaceutical products.

You will support the labeling and packaging of liquids, suspensions and lyophilized products, ensuring accuracy and compliance with safety and regulatory requirements. The role requires ability to read and follow written instructions in English, with 0–2 years of related experience.

Qualifications

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

Responsibilities

• 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

Skills

Visual inspection

Reading & following instructions

Teamwork

Education

High School Diploma or GED

Biotechnology certificate

Job description

Title: TEMP Inspection Labeling and Packaging Tech I (2nd shift) 1:30PM-10PM

Date: Sep 17, 2026

Company:

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
• 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