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...
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.
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