Quality Technician I - Batch Records Auditor

J&J Family of Companies; Añasco (PR); On-site; USD 36,000 - 48,000; Full time

Job summary

Johnson & Johnson in Anasco, Puerto Rico, seeks a Quality Technician I to audit batch records for completeness and correctness, maintain lot history, and generate NCRs, certificates, and reports as needed.

This role requires a high school diploma (associate degree preferred) and 2 years in a medical devices or pharmaceutical quality environment, with proficiency in Excel and Word and willingness to work overtime across shifts.

Qualifications

• High School diploma required; Associate’s Degree preferred.
• 2 years of experience in Medical Devices or Pharmaceuticals environment required.
• Experience in Quality and documentation preferred.
• Proficiency in Microsoft Excel and Word required.
• Availability to work overtime and various shifts, including weekends/holidays.

Responsibilities

• Audits all Batch Records for completeness and correctness across Processing, Packaging and Inspections.
• Manage Batch Records Retention process.
• Use computer systems for Inventory Transactions.
• Recommend redesigns of batch records for ease of use.
• Generate Quality, Compliance, and Analysis certificates as applicable.
• Perform activities related to product release or hold.
• Support ISO 14001 initiatives and environmental objectives.
• Train new personnel on Batch Record auditing (OJT).
• Adhere to Environmental, Safety and Industrial Hygiene policies.

Skills

Quality control

Batch records auditing

Documentation

Excel

Word

Overtime availability

Attention to detail

Education

High School diploma

Associate's Degree preferred

Tools

Microsoft Excel

Microsoft Word

Job description

Johnson & Johnson in Anasco, Puerto Rico, seeks a Quality Technician I to audit batch records for completeness and correctness, maintain lot history, and generate NCRs, certificates, and reports as needed.

This role requires a high school diploma (associate degree preferred) and 2 years in a medical devices or pharmaceutical quality environment, with proficiency in Excel and Word and willingness to work overtime across shifts.