Night Shift Quality Technician - Mon–Fri

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

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