2nd-Shift Quality Release Specialist

Abbott Laboratories; Santiago de Querétaro; Híbrido; MXN 180.000 - 240.000; Jornada completa

Descripción de la vacante

Abbott Laboratories in Querétaro is seeking a Quality Release Technician for the 2nd shift. The role involves final and in-process documentation review, product inspection, and supporting area release goals within the EP Electrophysiology division.

Ideal candidates hold a Bachelor's in Engineering with 1–2 years of relevant experience and proficiency in MS Office. GMP/ISO 13485 knowledge is desirable, with strong documentation practices and teamwork emphasized.

Formación

• Bachelor's degree in Engineering (or related field).
• 1–2 years in a similar quality/release role.
• Proficiency with MS Excel, Word, PowerPoint.
• Knowledge of GMP and ISO 13485 is desirable.
• Experience reviewing batch records and inspection reports.

Responsabilidades

• Perform in-process and final inspections against specifications and review device history records.
• Audit production operations and document inspections.
• Collect data, analyze results, and monitor critical-to-quality parameters.
• Assist in verifications, qualifications, and validations of equipment, products, and tests.
• Support release goals and maintain control plans to avoid line downtime.
• Help resolve nonconformances and improve documentation practices.
• Train and certify technicians on area procedures.
• Coordinate with team to set priorities and tasks.

Conocimientos

Attention to detail

Quality documentation

Problem solving

Educación

Bachelor's degree in Engineering

Herramientas

MS Excel

MS Word

MS PowerPoint

Descripción del empleo

Abbott Laboratories in Querétaro is seeking a Quality Release Technician for the 2nd shift. The role involves final and in-process documentation review, product inspection, and supporting area release goals within the EP Electrophysiology division.

Ideal candidates hold a Bachelor's in Engineering with 1–2 years of relevant experience and proficiency in MS Office. GMP/ISO 13485 knowledge is desirable, with strong documentation practices and teamwork emphasized.