Description

The GMP Associate I plays a vital role in the manufacturing of high-quality medical devices by operating equipment, packing finished products, loading automatic hoppers, and troubleshooting basic equipment issues through HMI (Human-Machine Interface) screens. This position requires strict adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and cleanroom standards, contributing to a safe and team-oriented environment.

Company Culture and Environment

The work environment promotes safety, teamwork, and a commitment to quality. Employees are encouraged to collaborate with various teams and uphold company values with professionalism while working in a cleanroom setting.

Career Growth and Development Opportunities

GMP Associates are provided with opportunities to participate in lean initiatives and complete a required lean curriculum for associate level, enhancing their skills and knowledge for potential career advancement.

Detailed Benefits and Perks

While specific benefits are not detailed, the emphasis on a safe and professional environment suggests a supportive workplace culture that values employee well-being and growth.

Compensation and Benefits

• Competitive hourly wage
• Opportunities for overtime
• Safe working conditions
• Team-oriented environment

Why you should apply for this position today

This position offers the chance to be part of a team that directly contributes to the manufacturing of essential medical devices. It’s a great opportunity for individuals looking to establish a career in the medical manufacturing field while ensuring high standards of quality and safety.

Skills

• Basic knowledge of HMI systems and cleanroom procedures
• Strong attention to detail and dedication to quality
• Ability to perform repetitive tasks and stand for long periods
• Willingness to wear full cleanroom PPE

Responsibilities

• Follow all safety procedures, including the proper use of PPE
• Adhere to cleanroom protocols and gowning requirements
• Maintain accurate documentation (batch records, logs, GDP)
• Perform in-process checks following GMP, FDA, and ISO 13485 standards
• Load hoppers and monitor material levels to avoid interruptions
• Assemble components and subassemblies per work instructions
• Operate production equipment and resolve basic HMI faults as needed
• Participate in lean initiatives (5S, Kaizen, QEK)
• Collaborate with Quality, Engineering, and other teams to achieve production goals

Qualifications

• High school diploma or equivalent
• Prior manufacturing or production experience preferred
• Basic knowledge of HMI systems and cleanroom procedures is a plus

Education Requirements

• High school diploma or equivalent

Education Requirements Credential Category

• High School Diploma

Experience Requirements

• Prior experience in a manufacturing or production environment is preferred

Why work in Clinton, PA

Clinton, PA, provides a serene environment with access to nature, fostering a balanced lifestyle. The community is known for its supportive atmosphere, making it an ideal place for both personal and professional growth.