GMP Associate III (Weekend Overnight)

Haemonetics•Clinton, PA

7d•Onsite

About The Position

The GMP Associate III serves as an area expert across all manufacturing lines, qualified and trained to operate every piece of equipment in the assigned area. This role builds upon the skills of GMP Associate I and II by providing technical leadership, troubleshooting, and guidance to less experienced associates. With a strong focus on safety, quality, and output, the GMP Associate III is the go-to resource for GMP I and GMP II team members, ensuring production goals are consistently met while maintaining compliance with all GMP, GDP, FDA, ISO 13485, and safety requirements. The working schedule for this role is Thursday night into Monday Morning, 4x10-hour shifts.

Requirements

High school diploma or equivalent required; technical certification or additional training preferred.
2–4 years of experience in a GMP-regulated manufacturing environment (medical device, pharmaceutical, or biotech preferred).
Fully qualified and trained on all equipment within the manufacturing area.
Strong understanding of GMP, GDP, FDA, and ISO 13485 compliance standards.
Demonstrated ability to troubleshoot and resolve complex equipment and process issues.
Proven track record of mentoring, coaching, or providing guidance to peers.
Excellent attention to detail, problem-solving, and communication skills.
Comfortable working in a fast-paced, team-driven environment.
Stand for extended periods; perform repetitive tasks.
Lift/move up to 25 lbs as needed.
Wear cleanroom attire (gown, mask, gloves) for prolonged periods.

Responsibilities

Act as a role model for safe work practices and adherence to PPE standards.
Support supervisors in identifying and mitigating safety risks on the floor.
Provide guidance and reinforcement to GMP I and II associates on safe equipment operation.
Uphold the highest standards of cleanroom discipline, documentation, and GMP compliance.
Serve as a subject matter expert in GDP, reviewing and supporting accurate completion of production and equipment records.
Perform and verify in-process inspections to ensure product quality meets all specifications.
Operate, troubleshoot, and maintain all equipment across the manufacturing area, ensuring flexibility and reliability.
Lead by example in loading/replenishing materials, packaging, and assembly tasks.
Ensure consistent throughput by proactively resolving technical issues and minimizing downtime.
Support and oversee TPM (Total Preventive Maintenance) activities, ensuring proper execution and follow-up.
Act as the go-to resource for GMP I and GMP II associates technical questions, troubleshooting, and process guidance.
Provide informal on-the-job training and coaching for team members.
Collaborate closely with Production Supervisors, Quality, and Engineering to identify and implement improvements.
Drive lean initiatives, including 5S, Kaizen, and problem-solving events.
Contribute expertise in identifying root causes of issues and implementing sustainable solutions.
Recommend process improvements to enhance safety, efficiency, and product quality.
Embody and reinforce company values in daily interactions.
Foster a culture of teamwork, accountability, and continuous learning.
Support production leadership by helping to set a professional and disciplined tone on the floor.
Uphold company policies and procedures, performing additional duties as needed to support production.
Communicate effectively with supervisors and team members to resolve issues and ensure smooth production flow.

Benefits

401(k) with up to a 6% employer match and no vesting period
employee stock purchase plan
flexible time off for salaried employees
accrual of three to five weeks’ vacation annually (based on tenure) for hourly employees
accrual of up to 64 hours (annually) of paid sick time
paid and/or floating holidays
parental leave
short- and long-term disability insurance
tuition reimbursement
health and welfare benefits