Parenteral Manufacturing Technician

Bristol Myers Squibb seeks a Parenteral Manufacturing Technician for rotating shift work at their Manati, Puerto Rico facility. The role involves executing parenteral manufacturing operations, maintaining compliance with cGMP standards, and supporting cross-functional quality and validation activities in a regulated pharmaceutical environment.

Responsibilities

• Set up, operate, and clean parenteral manufacturing equipment following approved standard operating procedures
• Execute formulation, sterilization, and filling processes including CIP/SIP operations and filter integrity testing
• Maintain accurate batch records and production documentation in real-time following Good Documentation Practices
• Perform environmental monitoring, quality investigations, and support validation and qualification activities
• Ensure housekeeping, safety compliance, and proper handling of hazardous materials in controlled environments

Requirements

• High school diploma or equivalent
• Minimum 2 years parenteral/aseptic manufacturing or 3 years pharmaceutical manufacturing experience
• Knowledge of formulation, preparation, and sterile filling operations
• Experience with automated or computer-controlled production equipment in regulated settings preferred
• Proficiency in Good Documentation Practices and data integrity principles
• Understanding of aseptic techniques and contamination control standards