GMP Manufacturing Associate II (Weekend Overnights)

Haemonetics Software Solutions; Pennsylvania; On-site; USD 28,000 - 43,000; Full time

Benefits offered by this job

401(k) with employer match

Employee stock purchase plan

Flexible time off

Vacation accrual (3–5 weeks)

Job summary

Haemonetics Software Solutions is seeking a cGMP II – Weekend Floater / Vacation Relief Team member for plasma manufacturing operations. The role builds on the cGMP I foundation, performing production tasks and supporting the Area Leader to meet production, quality, and safety goals.

The schedule is Thursday through Sunday 10-hour shifts (6:30 PM–4:00 AM) with high flexibility for vacation coverage and changing areas and responsibilities.

Qualifications

• 1–2 years of experience in a GMP-regulated manufacturing environment.
• Strong understanding of GMP/GDP principles.
• Experience with equipment operation and troubleshooting.
• Cleanroom experience preferred.
• Strong teamwork, communication, and attention to detail.
• Basic computer and manufacturing system skills.

Responsibilities

• Operate and troubleshoot GMP equipment to ensure production flow.
• Maintain cleanroom standards and document records.
• Support Total Preventive Maintenance (TPM) activities.
• Train new associates in GMP practices and equipment operation.
• Escalate issues to maintenance/engineering and improve processes.

Skills

GMP knowledge

Attention to detail

Teamwork

Education

High school diploma or equivalent

Job description

Job Details

Pay Transparency: The pay range for this role is: $19.90-$30.80/Hourly The base pay actually offered to the successful candidate will take into account, without limitation, the candidate’s location, education, job-knowledge, skills, and experience in prior relevant roles. Incentives may also be provided as part of Haemonetics’ employee compensation. For sales roles, employees will be eligible for sales incentive (i.e., commission) under the applicable plan terms. For non-sales roles, employees will be eligible for a discretionary annual bonus, the target amount of which varies based on the applicable role, to be governed by the applicable plan terms. Employees may also be eligible to participate in the Company’s long-term incentive plan, with eligibility and target amount dependent on the role.

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

Depending on your location, you may be eligible for more detailed information related to the compensation and benefits related to this job posting. If you believe you may be entitled to such information by law, you may contact 1-781-348-7777, Monday through Friday, 7:30 a.m. – 5 p.m. ET or email [e-mail]. 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 Summary

cGMP II – Weekend Floater / Vacation Relief Team The cGMP II is a skilled operator position on the weekend floater vacation relief team within Plasma manufacturing operations. Building on the foundation of the cGMP I role, this position performs production tasks while providing support and assistance to the Area Leader to help ensure the team meets production, quality, and safety goals.

Schedule

Thursday through Sunday 10-hour shifts: 6:30 PM – 4:00 AM. Highly flexible schedule that may change based on vacation coverage needs. Frequent changes in assigned areas and job responsibilities.

Key Accountabilities

• Demonstrate proficiency on all machinery and processes across Plasma departments
• Perform production tasks accurately, efficiently, and in full compliance with cGMP standards
• Assist the Area Leader with daily coordination, task prioritization, and team support
• Help train and coach cGMP I team members as needed
• Identify and communicate issues, deviations, or opportunities for improvement
• Support a culture of accountability, safety, and continuous improvement
• Remain flexible and adaptable to changing priorities, areas, and work assignments

This role is ideal for reliable, experienced operators who can work independently, support leadership, and contribute to the overall success of the weekend team. The GMP Associate II builds on the skills of Associate I by independently operating and troubleshooting manufacturing equipment, maintaining production flow, and ensuring compliance with GMP, GDP, and safety standards. This role also assists with training new associates, supports continuous improvement projects, and contributes to the consistent delivery of safe, effective medical devices.

Key Responsibilities

• Safety
  • Adhere to PPE and machine operation safety procedures. Report hazards, malfunctions, and incidents promptly.
• Quality
  • Maintain cleanroom standards and enforce gowning compliance. Complete and review production records, logs, and maintenance documentation. Perform in-process inspections and ensure products meet specifications.
• Manufacturing & Delivery
  • Load/replenish materials and ensure continuous production flow. Assemble components/subassemblies per GMP and work instructions. Operate equipment, diagnose and resolve HMI/automation faults, and perform equipment adjustments or troubleshooting. Escalate complex technical issues to maintenance/engineering. Perform cleaning, sanitization, and equipment care per SOPs. Take ownership of Total Preventive Maintenance (TPM) activities to ensure equipment reliability and readiness.
• Continuous Improvement & Training
  • Actively contributes to process improvements and waste reduction initiatives. Support lean practices and problem-solving activities. Assist with onboarding and training new associates in GMP practices and equipment operation.

Company Values

Work cross-functionally with Quality and Engineering to meet/exceed production targets. Act as a role model for professionalism and compliance. 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.

Qualifications

• High school diploma or equivalent.
• 1–2 years of experience in a GMP-regulated manufacturing environment (medical device, pharma, or biotech preferred).
• Strong understanding of GMP/GDP principles.
• Experience with equipment operation and troubleshooting.
• Cleanroom experience preferred.
• Strong teamwork, communication, and attention to detail.
• Basic computer and manufacturing system skills.

Physical Requirements

• Stand for extended periods; perform repetitive tasks.
• Lift/move up to 25 lbs as needed.
• Wear cleanroom attire (gown, mask, gloves) for prolonged periods.

EEO Policy Statement

Throughout our history, we have earned a solid reputation for product innovation, technical expertise, and operational excellence. Today, our products, internal research and development, marketing partnerships, and product acquisitions reflect our unwavering commitment to provide safe and available blood for patient transfusions and for use in pharmaceuticals. We rely on our talented global workforce to help us achieve our mission of providing innovative medical devices that advance the safety, quality, and availability of the world’s blood supply. To achieve our business goals and objectives, we are committed to attracting and retaining the best and brightest talent while offering a challenging, dynamic, and exciting work environment that offers professional growth and development.