Tech, QA Assurance - Shift C (Week Nights)

Baxter; Aibonito (PR); On-site; USD 30,000 - 47,000; Full time

Benefits offered by this job

Healthcare from day one

401(k) with company match

Employee Stock Purchase Plan (ESPP)

Paid holidays and PTO 20–35 days

Educational assistance

Job summary

Baxter International in Puerto Rico is seeking a Quality Technician to ensure our manufacturing processes meet the highest quality standards. You will revise documentation, perform audits, and support data-driven improvements aligned with GMP and company policies.

The role requires a Bachelor's in Science and at least two years in the Medical Device field, along with English/Spanish bilingual abilities. This on-site night-shift position offers comprehensive benefits and career growth within

Qualifications

• Bachelor's degree in Science.
• At least two years of related job experience in the Medical Device Industry.
• Proficiency in Data Entry and Microsoft Office Software, with basic computer knowledge required.
• Experience with measurement instrumentation.
• Excellent interpersonal skills.
• Willingness to travel occasionally.
• Bilingual (English & Spanish).

Responsibilities

• Revise and approve all documentation related to areas of responsibility, including In Process Checker Charts, Product Retention Records, Control Charts, Mold Approvals, Batch Records, and more.
• Conduct routine manufacturing audits of machine parameters and set-ups to ensure compliance, as well as audits of the manufactured product.
• Perform routine audits of sampling techniques, testing skills, and all documentation performed by the TIQ's.
• Immediately notify and raise awareness to Quality Management about potential quality situations.
• Assist and coordinate protocols to ensure detailed execution.
• Provide training on Good Documentation Practices, SPC, Total Coordinated Quality, and other relevant areas.
• Support mold approval and mold start-up evaluations, if applicable.
• Gather, analyze, audit, and interpret data using SPC methods to predict trends and recommend process improvements that positively impact product quality, scrap reduction, DPM reduction, complaints reduction, and price of non-conformance reduction.
• Maintain, revise, and audit control charts, computing control chart limits as needed.
• Ensure that all machinery, equipment, tools, and supervisory materials align with Corporate, GMP, and other regulatory requirements.
• Publish monthly Quality Indicators, including DPM's and Pareto Analysis, within your areas of responsibility.
• Submit improvements and modifications to specifications and Standard Operating Procedures.
• Maintain timely communication and awareness of DPM and complaints trends with internal and external customers/suppliers, if applicable.
• Assist in the development and certification of TIQ's.
• Perform special projects related to your areas of responsibility.
• Document required information manually (e.g., checker charts) and electronically (e.g., POMs) to align with applicable procedures and specifications.
• Conduct EHS inspections to identify and mitigate safety hazards and environmental aspects, analyze EHS incidents, and take corrective actions.
• Observe data privacy policies at all times.
• Provide support for software application audits.
• Assist in the generation and investigation of non-conformities.

Skills

Data entry

Microsoft Office

Measurement instrumentation

Interpersonal skills

Bilingual English/Spanish

Willingness to travel

Education

Bachelor's degree in Science

Job description

This is whereyour work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Work shift: Shift C (Week Nights)
Your role at Baxter:

As a Quality Technician, you will play a pivotal role in ensuring that our manufacturing processes and methods meet the highest standards of quality and compliance. Your expertise will be essential in maintaining the integrity of our Quality System Regulation, ensuring that every product we produce is detailed and meets our outstanding standards.

Beneficios y Horario de Trabajo

• Horario: Disponibilidad completa para trabajar en el turno nocturno durante la semana. 10:00pm - 6:30am Lunes a Viernes
• Diferencial por turno
• Vacaciones y días feriados pagados
• Cobertura de seguro médico, dental, por incapacidad y de vida
• Seguro de visión y beneficios voluntarios (Desde el dia 1)
• Licencia Maternidad y Paternidad remunerada
• Plan de ahorro para el retiro 165e
• Programa de compra de acciones para empleados
• Plan de asistencia educativa

Your team:

Baxter prioritizes the development of high-quality products that address patient needs. Our team is dedicated to putting patients first and takes pride in the value we deliver. Joining our multinational organization offers the opportunity to collaborate with diverse individuals, explore different areas of our portfolio, and receive ongoing support from our leadership team for personal growth.

What you'll be doing:

• Revise and approve all documentation related to areas of responsibility, including In Process Checker Charts, Product Retention Records, Control Charts, Mold Approvals, Batch Records, and more.
• Conduct routine manufacturing audits of machine parameters and set-ups to ensure compliance, as well as audits of the manufactured product.
• Perform routine audits of sampling techniques, testing skills, and all documentation performed by the TIQ's.
• Immediately notify and raise awareness to Quality Management about potential quality situations.
• Assist and coordinate protocols to ensure detailed execution.
• Provide training on Good Documentation Practices, SPC, Total Coordinated Quality, and other relevant areas.
• Support mold approval and mold start-up evaluations, if applicable.
• Gather, analyze, audit, and interpret data using SPC methods to predict trends and recommend process improvements that positively impact product quality, scrap reduction, DPM reduction, complaints reduction, and price of non-conformance reduction.
• Maintain, revise, and audit control charts, computing control chart limits as needed.
• Ensure that all machinery, equipment, tools, and supervisory materials align with Corporate, GMP, and other regulatory requirements.
• Publish monthly Quality Indicators, including DPM's and Pareto Analysis, within your areas of responsibility.
• Submit improvements and modifications to specifications and Standard Operating Procedures.
• Maintain timely communication and awareness of DPM and complaints trends with internal and external customers/suppliers, if applicable.
• Assist in the development and certification of TIQ's.
• Perform special projects related to your areas of responsibility.
• Document required information manually (e.g., checker charts) and electronically (e.g., POMs) to align with applicable procedures and specifications.
• Conduct EHS inspections to identify and mitigate safety hazards and environmental aspects, analyze EHS incidents, and take corrective actions.
• Observe data privacy policies at all times.
• Provide support for software application audits.
• Assist in the generation and investigation of non-conformities.

What you'll bring:

• Bachelor's degree in Science.
• At least two years of related job experience in the Medical Device Industry.
• Proficiency in Data Entry and Microsoft Office Software, with basic computer knowledge required.
• Experience with measurement instrumentation.
• Excellent interpersonal skills.
• Willingness to travel occasionally.
• Bilingual (English & Spanish).

US Benefits at Baxter (except for Puerto Rico)

• We are health and well-being benefits include medical and dental coverage that start on day one.
• insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance.
• Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount.
• the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching.
• We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave.
• Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits.
• Join us and enjoy the competitive compensation and benefits we offer to our employees.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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PO Box 1389 Road 721 Km 3|Aibonito, PR 00786|United States of America