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Production Operator

Job

Astrix Inc

Cranbury Township, NJ (In Person)

$58,240 Salary, Full-Time

Posted 1 day ago (Updated 8 hours ago) • Actively hiring

Expires 6/14/2026

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Job Description

Our client, a global leader in personal care products, is seeking experienced Production Operators to join their team in a GMP-regulated manufacturing environment. This is a contract opportunity with strong potential for permanent conversion based on performance and business needs.
Position Details Title:
Production Operator Location:
Cranbury, NJ (Fully Onsite)
Schedule:
1st Shift | Approximately 7:00 AM - 3:30/4:00 PM (hours may fluctuate based on production needs)
Duration:
Minimum 3-month contract with potential for full-time conversion
Pay Rate:
$26-$30/hour DOE We are specifically seeking candidates with hands-on experience in regulated pharmaceutical, CDMO, biotech, or GMP manufacturing environments. Ideal candidates will have experience supporting packaging and manufacturing operations, operating production equipment, completing batch documentation, and working within strict SOP and compliance requirements. Preferred Background & Experience Strong candidates will have experience with: GMP or regulated manufacturing environments Pharmaceutical or clinical manufacturing operations Packaging line operation and equipment setup Bottling, blister packaging, labeling, cartoning, kitting, or secondary packaging Line clearances, changeovers, and troubleshooting Batch records, GDP documentation, and SOP compliance Manufacturing Operator or Packaging Technician responsibilities Working closely with QA and compliance teams Position Summary Under minimal supervision, the Production Operator will support pharmaceutical manufacturing and packaging operations in a GMP environment. This role is responsible for operating manufacturing equipment, supporting development and production activities, maintaining documentation, and assisting with continuous improvement initiatives. Key Responsibilities Operate pharmaceutical manufacturing and packaging equipment in compliance with GMP and SOP requirements Perform equipment setup, operation, cleaning, line clearances, and changeovers Complete batch documentation and maintain accurate GDP records Support material sampling, staging, dispensing, and reconciliation activities Conduct in-process inspections and sampling activities Assist with troubleshooting production processes and equipment issues Support developmental manufacturing experiments and process improvements Assist maintenance teams with preventative maintenance and equipment support Participate in quality systems, compliance initiatives, and continuous improvement activities Follow all safety, regulatory, and company policies and procedures Utilize internal systems and software platforms for production documentation and reporting Qualifications Bachelor's degree in Engineering or a Scientific field with 1+ year of pharmaceutical or life sciences manufacturing experience OR High School Diploma/GED with 4+ years of pharmaceutical manufacturing experience, preferably involving new equipment implementation or process support Required Skills Knowledge of cGMP and pharmaceutical manufacturing practices Ability to read and interpret SOPs, batch records, work instructions, and technical documents Strong attention to detail and documentation accuracy Mechanical aptitude and troubleshooting ability Basic computer proficiency including data entry and email systems Ability to work independently and collaboratively in a team environment Strong communication and problem-solving skills Physical Requirements Ability to stand and walk for extended periods Frequent use of hands and arms during equipment operation Ability to lift up to 50 lbs preferred Ability to bend, stoop, kneel, crouch, and climb as needed Additional Information Fully onsite position, Monday-Friday Less than 5% travel required Opportunity to join a high-performing manufacturing team within a regulated pharmaceutical environment •This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you•INDBH #LI-DNI

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