Senior Validation & Process Engineer

Baxter International Inc.

Jayuya (PR)

Presencial

USD 90.000 - 130.000

Jornada completa

Hace 6 días
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Ventajas ofrecidas por este puesto de trabajo

Vacation and paid holidays
Medical, dental, disability and life保险
Vision and voluntary benefits
Educational assistance plan
Employee stock purchase plan

Descripción de la vacante

Baxter International Inc. is seeking a Senior Process Engineer to lead manufacturing process improvements in a fast-paced environment. You will coordinate projects, supervise maintenance upgrades, and ensure adherence to cGMPs and FDA regulations.

The role requires a strong background in engineering or sciences, 5+ years in related areas, and willingness to travel. Join a team that emphasizes innovation and professional growth in a mission-driven company.

Formación

  • 5+ years of experience in product development, change control, validations, or related areas.
  • Master's degree or PhD with at least 1–2 years of experience will be equivalent.

Responsabilidades

  • Perform, coordinate, and exercise functional authority for planning, organization, control, and completion of engineering maintenance and process upgrade tasks.
  • Coordinate plant schedule and resources within assigned manufacturing area.
  • Lead technical developments, scheduling, and resolve engineering design and test problems.
  • Evaluate and approve design changes, specifications, and drawing releases.
  • Ensure compliance with cGMP, safety and FDA regulations.
  • Mentor and develop team members; manage multiple projects and deadlines.

Conocimientos

Process engineering
Manufacturing
Project management
Leadership
Communication

Educación

Bachelor's degree in Engineering or Sciences
Master's or PhD (plus 1–2 years experience equivalence)

Descripción del empleo

Baxter International Inc. is seeking a Senior Process Engineer to lead manufacturing process improvements in a fast-paced environment. You will coordinate projects, supervise maintenance upgrades, and ensure adherence to cGMPs and FDA regulations.

The role requires a strong background in engineering or sciences, 5+ years in related areas, and willingness to travel. Join a team that emphasizes innovation and professional growth in a mission-driven company.

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