GMP Manufacturing Associate I - Cleanroom & Lean

haemonetics; Pennsylvania; On-site; USD 37,440 - 49,920; Full time

Benefits offered by this job

401(k) match

Stock purchase plan

Flexible time off

Vacation

Paid sick time

Holidays

Parental leave

Disability insurance

Tuition reimbursement

Health benefits

Job summary

Haemonetics is seeking a GMP Associate I in Pennsylvania to support the manufacture of high‑quality medical devices. You will operate equipment, pack finished products, and resolve basic equipment faults via HMI, while following GMP, GDP and cleanroom standards.

You will work on a 2‑2‑3 schedule (6:30AM–6:30PM), with focus on safety, quality, and continuous improvement. Prior manufacturing experience is a plus, and you’ll contribute to a collaborative, metrics‑driven team.

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.
• This position operates on a 2-2-3 schedule. 6:30AM-6:30PM.

Responsibilities

• Follow all safety procedures, including PPE.
• Adhere to cleanroom protocols and gowning requirements.
• Maintain accurate, compliant documentation (batch records, logs, GDP).
• Operate production equipment and resolve basic HMI faults, escalating as needed.
• Perform routine cleaning and sanitization of equipment and workspace.
• Participate in lean initiatives (5S, Kaizen, QEK).

Skills

Attention to detail

Quality minded

Lean manufacturing

Education

High school diploma or equivalent

Tools

HMI systems

Job description

Haemonetics is seeking a GMP Associate I in Pennsylvania to support the manufacture of high‑quality medical devices. You will operate equipment, pack finished products, and resolve basic equipment faults via HMI, while following GMP, GDP and cleanroom standards.

You will work on a 2‑2‑3 schedule (6:30AM–6:30PM), with focus on safety, quality, and continuous improvement. Prior manufacturing experience is a plus, and you’ll contribute to a collaborative, metrics‑driven team.