Night-Shift Manufacturing Lead: Quality & Efficiency

Baxter International Inc.; Aibonito (PR); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Dental coverage

401(k) plan

ESPP

Paid time off

Job summary

Baxter International Inc. in the United States is seeking a manufacturing supervisor for shift C (10:00pm - 6:00am) to oversee assembly and packing operations. You will ensure compliance with manufacturing and quality regulations while delivering high quality, service and low cost.

You will supervise team members, train new staff, coordinate code changes, monitor process quality and performance, and drive continuous improvements in a FDA-regulated environment. Bilingual English/Spanish required.

Qualifications

• BA or BS in Engineering or related field with 1–3 years of manufacturing experience.
• One-year supervisory experience in a manufacturing FDA-regulated environment.
• Bilingual in English and Spanish.

Responsibilities

• Supervise assembly and packing operations within a manufacturing cell.
• Address equipment, materials, and personnel issues.
• Maintain absenteeism per Baxter policy.
• Train and evaluate new employees; plan cross-training.
• Motivate and coordinate the workforce.
• Supervise code changes; monitor quality and performance.
• Promote a world-class environment through teamwork and suggestions.
• Drive process improvements; evaluate complaints data.
• Know Baxter specifications and GMP-QSR, OSHA, SOP, HR policies.
• Document process parameters, lots, and production data.
• Promote zero-harm workplace and ensure EHS resources.

Skills

Bilingual (English/Spanish)

Interpersonal skills

Communication

GMP-QSRs knowledge

Education

Bachelor's degree in Engineering or related field

Job description

Baxter International Inc. in the United States is seeking a manufacturing supervisor for shift C (10:00pm - 6:00am) to oversee assembly and packing operations. You will ensure compliance with manufacturing and quality regulations while delivering high quality, service and low cost.

You will supervise team members, train new staff, coordinate code changes, monitor process quality and performance, and drive continuous improvements in a FDA-regulated environment. Bilingual English/Spanish required.