Materials QA Technician

Mykelly; Caguas (PR); On-site; USD 17,000 - 24,000; Full time

Benefits offered by this job

Weekly pay

Health Insurance

Paid vacations & holidays

Christmas bonus

Job summary

Kelly Life Science is seeking a Materials QA Technician to join a leading medical device company in Puerto Rico East. This role focuses on QA sampling, material handling, and documentation within a regulated manufacturing setting.

The position offers a 2nd shift, $15 per hour, benefits, and weekly pay. Travel between Caguas, Gurabo, San Lorenzo, Vega Alta, and Manatí is required with mileage reimbursement; bilingual English/Spanish communication is essential.

Qualifications

• Associate degree required in natural sciences or related discipline.
• Minimum 1 year in QA, QC, materials management, or related role in a regulated industry; medical device experience preferred.
• Knowledge of quality systems, regulatory requirements, and inventory systems.

Responsibilities

• Coordinate, transport, inspect, and document QA samples and non-conforming materials in a regulated manufacturing environment.
• Support quality operations, HOLD cage inventory, sterilization prep, and segregate non-conforming batches.
• Perform relabeling, verify inventory, investigate discrepancies, and maintain batch records.
• Conduct compliance audits, support process improvements, and participate in projects.
• Ensure adherence to safety, quality, and regulatory standards.

Skills

Quality Assurance

Quality Control

Materials Management

Regulated industry

Documentation control

Bilingual English/Spanish

Attention to detail

Cross-functional teamwork

Problem-solving

Education

Associate degree in Natural Sciences

Tools

MES

Job description

Put your career in motion with a great, new opportunity.

Join Kelly®Life Science team as Materials QA Technician to work at a leading medical device company in east area.

This opportunity could be the one you’ve been looking for.

Why should you apply to be Materials QA Technician:

Salary : $15per hour plus benefits

Shift : 2nd Shift

Location: Puerto Rico east area (needs to be onshore),travel regularly between Caguas, Gurabo, San Lorenzo, Vega Alta, and Manatí. Mileage and toll reimbursement will be provided according to company policy.

• Competitive pay rate and comprehensive fringe benefits
• Work in a regulated environment with a respected industry leader
• Opportunity to gain valuable experience in Medical Device Manufacturing
• Mileage and toll reimbursement provided for authorized business travel
• Supportive team culture focused on safety, quality, and continuous improvement
• Weekly pay by W-2
• Health Insurance
• Vacations, Sick & Holidays paid*
• Christmas bonus*
  • *Must comply with minimum established requirements to qualify.

Requirements:

• Associate degree in Natural Sciences or a related scientific discipline required.
• Minimum one (1) year of experience in Quality Assurance, Quality Control, Materials Management, Warehouse Operations, or a related role within a regulated industry; Medical Device industry experience strongly preferred.
• Working knowledge of quality systems, regulatory compliance requirements, and inventory management systems (MES experience preferred).
• Strong attention to detail with experience in documentation control, inventory accuracy, and discrepancy investigations.
• Excellent organizational, analytical, communication (Spanish and English proficient), and problem-solving skills, with the ability to work independently in a cross-functional environment.
• Valid driver's license and a reliable personal vehicle in good operating condition (larger vehicles such as SUVs, crossovers, or spacious sedans preferred)

Responsibilities:

• Coordinating, transporting, handling, inspecting, and documenting QA samples and non-conforming materials within a regulated manufacturing environment.
• Supporting quality operations, including managing HOLD cage inventory, preparing pallets for sterilization, and removing or segregating non-conforming batches.
• Performing re-labeling activities, verifying inventory, investigating discrepancies, and maintaining accurate batch records.
• Conducting compliance audits, supporting process improvements, and participating in departmental projects.
• Ensuring adherence to all company safety, quality, and regulatory standards.

Helping you discover what’s next in your career is what we’re all about, so let’s get to work.

Lilly Abouomar 9395454792 #SETTPuertoRico #MedicalDevices#PR#QA #Quality#Kelly80