Jobs · Engineering · New Jersey

Production Operator-2nd shift

Jobright.ai · Cranbury, NJ · 6 days ago
On-siteEngineering$20–$25/hrFull-time

This role is part of the Jobright Direct Hiring Network, where top companies hire top talent directly through our platform.

About the company

LinQ Global Group is a global professional services and staffing firm connecting small and mid-sized businesses with IT, healthcare, and engineering talent across the US, Canada, and India. The company supports clients in regulated pharmaceutical manufacturing, including cGMP cleanroom and specialized equipment environments, with a leadership team boasting over 25 years of technology and staffing experience.

Responsibilities

  • Execute end-to-end manufacturing operations, including materials dispensing, granulation, sifting, milling, and drying workflows.
  • Set up, operate, and closely monitor specialized machinery for the compression, encapsulation, and coating of solid-dosage products.
  • Master the mechanical disassembly, technical setup, and verification of high-speed pharmaceutical production machinery.
  • Wash, sanitize, and deep-clean all processing equipment and mechanical parts according to rigid cleanroom SOPs.
  • Complete all master batch records, material tracking logs, and yield calculations accurately and legibly in English.
  • Follow all approved Standard Operating Procedures, chemical Safety Data Sheets (SDS), and batch protocols without deviation.
  • Ensure assigned manufacturing suites are cleaned, organized, and maintained following good housekeeping practices.
  • Actively identify line anomalies, clear operational jams, and perform minor mechanical adjustments to minimize processing downtime.
  • Participate transparently in formal Quality Investigations, deviance tracking, and root-cause analyses alongside compliance teams.
  • Securely don all required Personal Protective Equipment (PPE), including full or partial facepieces according to OSHA standards.
  • Maintain impeccable personal hygiene habits and gowning standards required for a sterile processing environment.
  • Assist manufacturing management in executing commercial and experimental development runs efficiently to hit strict timelines.

Requirements

  • High School Diploma or GED equivalent.
  • Practical familiarity working inside a regulated environment, preferably a solid-dosage pharmaceutical manufacturing plant.
  • Hands-on experience setting up, operating, cleaning, and troubleshooting industrial processing equipment.
  • Excellent written and verbal English communication skills, with the capability to pass technical written and physical execution tests.
  • Demonstrated ability to manage multi-step processing schedules safely with minimal direct oversight.
  • Full capability to stand continuously for an 8-hour shift and lift/move processing materials weighing up to 30 lbs (14 kg) without assistance.
  • Fit-tested or capable of being certified to wear full and partial respiratory facepieces.

Qualifications (Preferred)

  • Bachelor's degree in the Physical Sciences, Chemistry, Biology, or a dedicated Pharmaceutical Life Science field of study.
  • Previous experience managing large-scale chemical blending, fluid-bed drying, or high-speed tablet press machinery.

Pay

$20/hr - $25/hr

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