Packaging Operator at Trident Consulting Inc

St. Louis, Missouri, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Jul, 26

Salary

22.0

Posted On

04 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Packaging, Labeling, Manufacturing operations, Batch records, Quality standards, GMP, Chemical handling, Documentation accuracy, SOP compliance, Safety regulations, Attention to detail, Laboratory procedures

Industry

IT Services and IT Consulting

Description

Company Description About Trident: Trident Consulting is an award-winning IT/engineering staffing company founded in 2005 and headquartered in San Ramon, CA. We specialize in placing high-quality vetted technology Some of our recent awards include: 2022, 2021, 2020 Inc. 5000 fastest-growing private companies in America 2022, 2021 SF Business Times 100 fastest-growing private companies in Bay Area Job Description Job Title: Packaging Operator / Manufacturing Operator I Location: Round Rock, TX Duration: 6 Months Contract (Potential Extension) Schedule: Monday – Friday, 8:00 AM – 5:00 PM Pay Rate: $21 – $22 per hour Job Summary The Packaging Operator (Manufacturing Operator I) is responsible for supporting production operations by performing labeling, relabeling, and packaging of reference standard solutions and neat material aliquots used in life science products. The role ensures that all packaging and labeling processes are completed accurately, safely, and in compliance with company quality standards and regulatory guidelines. The operator will work closely with production teams to meet daily manufacturing targets while maintaining a clean and safe work environment. Key Responsibilities Perform labeling, relabeling, and packaging of reference standard solutions and chemical materials according to documented procedures. Prepare and complete batch records, production forms, and documentation required for packaging operations. Review batch records and packaging documentation to ensure accuracy, completeness, and compliance before and after execution. Ensure all packaged materials meet quality standards, labeling accuracy, and regulatory requirements. Support production schedules by ensuring timely completion of packaging projects to meet operational goals. Communicate production delays, issues, or discrepancies to supervisors and relevant teams. Follow Good Manufacturing Practices (GMP), safety regulations, and company quality policies. Maintain cleanliness and organization of the work area following housekeeping and safety standards. Handle chemicals and packaging materials while using appropriate Personal Protective Equipment (PPE). Collaborate with team members to improve workflow efficiency and maintain productivity targets. Required Qualifications High School Diploma or GED required Associate degree preferred, ideally in a scientific or technical discipline Basic understanding of manufacturing or packaging operations Ability to follow written instructions, SOPs, and batch records Strong attention to detail and documentation accuracy Ability to work in a regulated production environment Preferred Qualifications Previous experience in life sciences, pharmaceutical, laboratory, or chemical manufacturing environment Familiarity with GMP, quality documentation, or batch records Experience with chemical handling, labeling systems, or packaging operations Physical & Work Environment Requirements Work may involve handling chemicals and laboratory materials with proper PPE. Position requires standing, repetitive tasks, and manual handling of packaging materials. Standard physical exam required based on job duties. Work performed in a controlled manufacturing or laboratory production environment. Interview Process First Round: Virtual Interview Second Round: On-site Interview Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

The Packaging Operator is responsible for performing labeling, relabeling, and packaging of reference standard solutions and chemical materials. They must ensure all production documentation is accurate and compliant with GMP and safety standards.