GMP Manufacturing Associate I - Medical Devices

Haemonetics Software Solutions; Pennsylvania; On-site; USD 34,000 - 52,000; Full time

Benefits offered by this job

401(k) with employer match

Employee stock purchase plan

Flexible time off

Paid vacation and holidays

Health and welfare benefits

Job summary

Haemonetics is seeking a GMP Associate I to support the manufacturing of high-quality medical devices. You will operate equipment, pack finished products, load hoppers, and troubleshoot basic HMI faults while adhering to GMP, GDP, and cleanroom standards.

This role emphasizes safety, quality, and teamwork in a lean environment. Responsibilities include maintaining documentation, performing in-process checks, and contributing to continuous improvement through lean initiatives.

Qualifications

• High school diploma or equivalent.
• Prior manufacturing or production experience preferred.
• Basic knowledge of HMI systems and cleanroom procedures a plus.
• Strong attention to detail and commitment to quality.
• Ability to stand for long periods and perform repetitive tasks.
• Willingness to wear full cleanroom PPE.

Responsibilities

• Follow safety procedures and wear PPE.
• Adhere to cleanroom protocols and GDP batch records.
• Operate production equipment and resolve basic HMI faults.
• Load hoppers and monitor material levels to prevent interruptions.
• Assemble components per work instructions and complete GDP paperwork.
• Participate in lean initiatives and complete required lean curriculum.

Skills

Attention to detail

HMI systems

Cleanroom procedures

Safety compliance

Physical stamina

Education

High school diploma or equivalent

Job description

Haemonetics is seeking a GMP Associate I to support the manufacturing of high-quality medical devices. You will operate equipment, pack finished products, load hoppers, and troubleshoot basic HMI faults while adhering to GMP, GDP, and cleanroom standards.

This role emphasizes safety, quality, and teamwork in a lean environment. Responsibilities include maintaining documentation, performing in-process checks, and contributing to continuous improvement through lean initiatives.