Night Shift Manufacturing Supervisor

Baxter Healthcare

Aibonito (PR)

On-site

USD 42,000 - 62,000

Full time

6 days ago
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Benefits offered by this job

Health benefits
401(k) plan
ESPP
Paid time off

Job summary

Baxter Healthcare Puerto Rico is seeking a Shift Supervisor for the assembly and packing area, working 10:00pm–6:00am, to ensure compliance with manufacturing and quality regulations. You will supervise operations, train staff, coordinate code changes, and monitor quality and performance.

A BA/BS in engineering with 1–3 years of manufacturing experience is required; bilingual English/Spanish is essential. Ideal candidates will have FDA-regulated manufacturing experience, strong interpersonal

Qualifications

  • BA OR BS in Engineering/ or related field with 1-3 years of manufacturing experience.
  • One-year previous supervisor in a manufacturing FDA regulated environment preferred.
  • Bilingual (English and Spanish).
  • Excellent interpersonal relations skills.
  • Must be knowledgeable of Baxter specifications and procedures. Strong knowledge of Baxter manufacturing process. Knowledge on GMP-QSR’S, OSHA, BHEST, SPEC, SOP and HR policies.

Responsibilities

  • Supervise all assembly operation including the packing area within a manufacturing cell.
  • Coordinate and supervise material, equipment and associate issues.
  • Maintain attendance and ensure Baxter policies.
  • Train and evaluate new employees; plan cross-training for staff.
  • Maintain a motivated workforce and promote teamwork.
  • Coordinate and supervise code changes and process monitoring.
  • Drive process improvements and cost reduction programs.
  • Document parameters, lots, production data per procedures.

Skills

Bilingual English/Spanish
Interpersonal skills
GMP/QSR knowledge
Process knowledge

Education

BA/BS in Engineering or related field

Job description

Baxter Healthcare Puerto Rico is seeking a Shift Supervisor for the assembly and packing area, working 10:00pm–6:00am, to ensure compliance with manufacturing and quality regulations. You will supervise operations, train staff, coordinate code changes, and monitor quality and performance.

A BA/BS in engineering with 1–3 years of manufacturing experience is required; bilingual English/Spanish is essential. Ideal candidates will have FDA-regulated manufacturing experience, strong interpersonal

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