GMP Associate I – Plant Manufacturing (Bottling)

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profile Job Location:

Clinton, UT - USA

profile Monthly Salary: Not Disclosed
Posted on: 9 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Title: GMP Associate I Plant Manufacturing (Bottling)
Location: Clinton PA (Onsite)
Duration: 05/27/2026 11/26/2026
Shift: A Team Bottles 2-2-3 Schedule 6:30 AM 6:45 PM

Job Summary

The GMP Associate I supports the manufacturing of high-quality medical devices in a cleanroom production environment. This role involves operating production equipment packaging finished products loading automatic hoppers completing GMP documentation and resolving basic equipment faults through HMI (Human-Machine Interface) systems.

The ideal candidate will maintain strict adherence to Good Manufacturing Practices (GMP) Good Documentation Practices (GDP) safety standards and quality procedures while contributing to a team-oriented manufacturing environment.

Key Responsibilities Safety
  • Follow all safety procedures and PPE requirements.
  • Report hazards equipment malfunctions and incidents promptly.
  • Maintain a clean and safe work environment.
Quality & Compliance
  • Adhere to cleanroom protocols and gowning requirements.
  • Maintain accurate and compliant documentation including batch records and production logs.
  • Perform in-process quality inspections and checks.
  • Follow GMP FDA and ISO quality standards.
Manufacturing Operations
  • Load hoppers and monitor material levels to prevent production interruptions.
  • Assemble components and subassemblies according to work instructions.
  • Perform bottling and packaging activities while ensuring accurate GDP documentation.
  • Operate manufacturing equipment and troubleshoot basic HMI-related faults.
  • Escalate equipment or process issues when necessary.
  • Perform routine cleaning and sanitization of equipment and work areas.
Continuous Improvement
  • Participate in Lean Manufacturing initiatives such as 5S Kaizen and QEK activities.
  • Complete required operational and continuous improvement training.
Team Collaboration
  • Work collaboratively with Quality Engineering and Operations teams to meet production goals.
  • Demonstrate professionalism and adherence to company policies and procedures.
Qualifications
  • High school diploma or equivalent required.
  • Previous manufacturing or production experience preferred.
  • Basic knowledge of HMI systems and cleanroom procedures is a plus.
  • Strong attention to detail and commitment to quality.
  • Ability to work in a fast-paced manufacturing environment.
  • Willingness to wear full cleanroom PPE for extended periods.
Physical Requirements
  • Ability to stand for extended periods during shifts.
  • Perform repetitive motions and production-related tasks.
  • Ability to lift and move up to 25 lbs as needed.
  • Ability to work while wearing cleanroom attire including gown gloves and mask.
Job Title: GMP Associate I Plant Manufacturing (Bottling) Location: Clinton PA (Onsite) Duration: 05/27/2026 11/26/2026 Shift: A Team Bottles 2-2-3 Schedule 6:30 AM 6:45 PM Job Summary The GMP Associate I supports the manufacturing of high-quality medical devices in a cleanroom produc...
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