Supervisor, Quality

Haemonetics; Tijuana; Presencial; MXN 538,000 - 809,000; Jornada completa

Descripción de la vacante

A leading healthcare company in Tijuana is looking for an Incoming Supervisor to coordinate quality inspectors and manage the quarantine area of production. This role involves overseeing inspections, ensuring compliance with regulations, and training staff on procedures. The ideal candidate should have a background in engineering or life science, with at least one year of experience in similar roles, including audits and problem-solving skills. Knowledge of GMP and ISO standards is essential.

Formación

• 1 year in a similar position required.
• Proven experience in coordinating and controlling quarantine areas required.
• Experience in process and customer audits required.

Responsabilidades

• Coordinate quality inspectors and verify starting operations.
• Oversee training of quality inspectors in procedures.
• Manage products in the quarantine area and ensure proper disposal.
• Monitor inspector in charge of product testing validation.

Conocimientos

Proficiency in product knowledge

Effective interpersonal skills

Demonstrated written communication skills

Strong verbal communication and listening skills

Excellent collaboration and team building skills

Excellent organizational skills

Demonstrated problem solving skills

Basic English skills

Educación

B in Engineering or Life Science discipline

Descripción del empleo

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 Details

Incoming Supervisor

Responsibilities

• Responsible for coordinating the group of quality inspectors, verify proper start of operations in areas of production, product official documents, and following the procedures for packaging and shipping process through quality inspectors.
• Responsible for overseeing that the quality inspectors are trained in the proper procedures for carrying out their work.
• Responsible for all products that are in the quarantine area, checking its management, control and destination.
• Responsible to ensure the proper disposal of the material found in the quarantine area.
• Responsible for monitoring the inspector in charge of product testing validation and introduction of new products.
• Responsible for maintaining quality, according to procedures, specifications and guidelines established within the plant.
• Responsible for the reporting of scrap that is generated by product testing. Perform visual and functional inspection applicable to the disposal of the product.
• Monitor daily diary compliance QSR and ISO compliance in the manufacturing floor. Ensures control of raw material, work in process, finished goods, and sterilized product to prevent release of materials and products not approved.
• With minimal direction conducts research on customer complaints as well as participate in the management of internal CAPA.
• Responsible for site internal audit coordination/internal auditor.
• Manage the Corrective Action Program processes (CAPA). Determine whether the actions proposed by the areas of manufacturing and manufacturing materials, keep track corrective actions, track these actions, and determine if the actions have been effective.
• Develop and write procedures and instructions for handling customer complaints.
• Engage quality engineering and direct actions required to correct defects.
• Prepares and provides tend reports.
• Must ensure compliance with all regulations, Mexican regulations and internal policies Haemonetics in health, safety and environmental.

Qualifications & Education

• B in Engineering or Life Science discipline or related technical field. Required.

Experience

• 1 year similar position. Required.
• Proven experience in the coordination and control of quarantine areas. Required.
• Proven experience in the coordination and control of quarantine areas. Required.
• Experience in process and customer audits. Required.
• Experience handling reports of materials, waste, material tested. Required.
• Proven experience in managing quality reports, production quantities and materials, in addition to statistical graphics. Required.

Skills

• Proficiency in product knowledge.
• Effective interpersonal skills.
• Demonstrated written communication skills.
• Strong verbal communication and listening skills.
• Excellent collaboration and team building skills.
• Excellent organizational skills.
• Maintains a high degree of professionalism.
• Assumes personal responsibility for actions.
• Demonstrates a high level of accuracy, even under pressure.
• Demonstrated problem solving skills.
• High degree of initiative.
• Flexibility to work in a fast paced, dynamic environment.
• Ability to learn and teach others.
• Knowledge of the processes and the use of variances, product specifications, and different units of measurement.
• Documentation management, product and process specifications, and handling measuring instruments for product testing.
• Management of common processes such as line inputs, production records for traceability, material requisition, discard, etc.
• Sampling handling on production lines.
• Basic English skills.

Training & Certifications

• Knowledge and experience in GMP, GDP's, ISO standards.
• Valid US Visa.

EEO Policy Statement