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2nd Shift Production Sterilization Specialist

Job in Ledgewood, Morris County, New Jersey, 07852, USA
Listing for: Harrow
Full Time position
Listed on 2026-08-03
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Production Associate / Production Line, Pharmaceutical Manufacturing
Job Description & How to Apply Below
Location: Ledgewood

2nd Shift Production Sterilization Specialist

Ledgewood, New Jersey

Harrow (Nasdaq: HROW) is a leading provider of ophthalmic disease management solutions in North America. Harrow is an incredible entrepreneurial company – where we celebrate the ability of every member of the Harrow Family to be the CEO of their job. Harrow's values have driven interest over the past decade in attracting high-performing professionals in a variety of disciplines. Members of our Harrow Family often express their pride in being a part of our commitment to (1) innovation, (2) patient access to affordable medicines, and (3) our track record of having never turned down an ophthalmologist doing mission work around the world – providing free medicines in support of mission work aimed at giving or maintaining the gift of sight to those most in need.

We encourage you to learn more about Harrow and its unique culture to see if you're the right person to help contribute as we build a truly exceptional company, one we are all so proud of!

Harrow's ophthalmic pharmaceutical portfolio is one of the most comprehensive in the industry, including:

  • An expanding Retina Portfolio including IHEEZO®, TRIESENCE®, BYOOVIZ™, and OPUVIZ™
  • A broad Dry Eye Disease product line, led by VEVYE® and bolstered by well-known adjacent ocular surface disease products such as FLAREX® and FRESHKOTE®
  • A peri-operative Surgical product line, led by TRIESENCE® and BYQLOVI™
  • A Rare and Specialty product line, which includes various high-need and utility products such as ILEVRO®, NATACYN®, and VERKAZIA®
  • A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01

The hours for this shift are 3pm - 1:30am

Job Summary

The Production Sterilization Specialist will be responsible for conducting labeling, packaging, and production support activities to support commercial manufacturing. Under the direction of the Production Supervisor/Team Leader, the Production Support Associate will work hands-on under ISO7, ISO8, and other classified areas with various manufacturing production equipment and technologies. Daily responsibilities vary, including operating cleaning machines and preparing supplies for manufacturing by cleaning and disinfecting.

Core Responsibilities

  • Ensures that all work is carried out in compliance with company Safety Policies, current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs).
  • Wears proper personal protective equipment and follows aseptic procedures when gowning, de-gowning, and working in sterile and controlled areas.
  • Reports any accidents, incidents, injuries, or illnesses immediately and notifies the manager of any workplace hazards, unsafe acts, or conditions.
  • Accurate completion of product documentation and all appropriate logbooks. Maintains cleaning logs per SOP requirements.
  • Knowledge of current Good Manufacturing Practices (cGMP) guidelines.
  • Excellent organization and time-management skills are required. Must promptly manage a heavy workload and aggressive timelines, prioritize, and work under pressure.
  • Cleaning, sanitizing, and disinfection of equipment and components required for production.
  • Works with the Warehouse Department to ensure all components are available ahead of time for production.
  • Completes all necessary cleaning and sanitizing of production equipment and area.
  • Stages material for production use.
  • Operation of cleaning equipment including but not limited to Autoclave, Fedegari, and Depyrogentation oven.
  • Performs calibration of check weighing.

Qualifications & Requirements

  • High School Diploma or equivalent work and education in a related field are required.
  • 1-3 years of experience working in the pharmaceutical industry and within aseptic clean room environments.
  • Demonstrated ability to successfully gown into aseptic manufacturing areas.
  • Ability to handle sensitive information with a high degree of confidentiality.
  • Ability to work in a fast-paced environment while demonstrating excellent time management and organization skills.
  • Proficient in using standard Microsoft Office software products, including Excel, Outlook, and Word.
  • Strong organizational skills with the proven ability to prioritize.
  • Works with a sense of urgency while engaging and listening to experts.

Position Type

  • On-Site

Travel

  • None
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