Quality Technician — Night Shift (Weeknights)

1098 BAXTER HEALTHCARE OF PUERTO RICO LLC; Aibonito (PR); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

401(k) with match

Employee stock purchase plan (ESPP)

Paid holidays

Paid time off

Parental leave

Job summary

Baxter in Puerto Rico is seeking a Quality Technician for the Week Night Shift (Shift C). You will ensure manufacturing processes and methods meet quality and compliance standards and support the Quality System Regulation.

You will review documentation, perform audits, and help maintain control charts. Ideal candidates have a science degree, 2+ years in the medical device industry, proficiency with Microsoft Office, and willingness to travel occasionally.

Qualifications

• Bachelor's degree in Science required.
• At least two years of related job experience in the Medical Device Industry preferred.
• Proficiency with Data Entry and Microsoft Office software is required.
• Experience with measurement instrumentation is preferred.
• Excellent interpersonal skills are essential.
• Willingness to travel occasionally.
• Bilingual English & Spanish is preferred.

Responsibilities

• Review and approve documentation related to areas of responsibility, including in-process charts, batch records, and control charts.
• Conduct routine audits of machine parameters and set-ups for compliance and product quality.
• Perform audits of sampling techniques, testing skills, and documentation performed by TIQ personnel.
• Notify Quality Management of potential quality issues.
• Provide training on documentation practices, SPC, and quality systems.

Skills

Data entry

Interpersonal skills

Bilingual English/Spanish

Willingness to travel

Education

Bachelor's degree in Science

Tools

Microsoft Office

Measurement instrumentation

Job description

Baxter in Puerto Rico is seeking a Quality Technician for the Week Night Shift (Shift C). You will ensure manufacturing processes and methods meet quality and compliance standards and support the Quality System Regulation.

You will review documentation, perform audits, and help maintain control charts. Ideal candidates have a science degree, 2+ years in the medical device industry, proficiency with Microsoft Office, and willingness to travel occasionally.