GMP Associate I 2-2-3 Schedule at Haemonetics

**Who this is for** This role is ideal for entry-level candidates looking to start a career in medical device manufacturing within a stable, team-oriented produ

Work type: onsite

Location: Clinton, PA

Type: Full-time

Summary

**Who this is for** This role is ideal for entry-level candidates looking to start a career in medical device manufacturing within a stable, team-oriented production environment. **Key highlights** You will play a crucial role in maintaining high-quality standards by operating production equipment, managing material flow, and ensuring strict adherence to FDA and ISO cleanroom protocols. **You might be a good fit if you...** - Have a high school diploma or equivalent and a strong commitment to quality standards. - Are comfortable working in a cleanroom environment while wearing required PPE. - Possess the ability to stand for long periods and lift up to 25 lbs consistently. - Demonstrate reliability and the ability to follow detailed work instructions and safety protocols.

Job Description

We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.

## Job Details

Job Summary

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

Key ResponsibilitiesSafety

• Follow all safety procedures, including the proper use of PPE.


• Report hazards, malfunctions, and incidents promptly.

• Adhere to cleanroom protocols and gowning requirements.


• Maintain accurate, compliant documentation (batch records, logs, GDP).


• Perform in-process checks and follow GMP, FDA, and ISO 13485 standards.

• Load hoppers and monitor material levels to avoid interruptions.


• Assemble components and subassemblies per work instructions.


• Execute activities in molding such as proper packaging and completion of GDP paperwork.


• 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).


• Complete required lean curriculum for associate level.

• Collaborate with Quality, Engineering, and other teams to achieve production goals.


• Uphold company values and policies with professionalism.


• Stand for extended periods; perform repetitive tasks.


• Lift/move up to 25 lbs as needed.


• Wear cleanroom attire (gown, mask, gloves) for prolonged periods.

• 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.

• Stand for extended periods; perform repetitive motions.


• Lift/move up to 25 lbs as needed.


• Wear cleanroom attire (gown, mask, gloves) for prolonged periods.

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