Senior Parenteral Manufacturing Technician
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Shift D (5pm to 530am)
PRINCIPAL OBJECTIVE OF POSITION
Responsible for different parenteral manufacturing operations in addition to the mechanical, electronic diagnosis and troubleshooting involving highly sensitive pharmaceutical/biologics products equipment.
This will include traditional aseptic process and/or Isolator Technology process.
This position must comply with all Security Guidelines, Environmental Health and Safety regulations, SOP’S and the current Good Manufacturing Practices.
MAJOR DUTIES AND RESPONSIBILITIES
* Perform mechanical evaluation and troubleshooting
* Performs initial evaluation and minor troubleshooting diagnosis of manufacturing equipment failures
* Supports maintenance personnel in major troubleshooting diagnosis activities.
* Performs complex and highly technical manufacturing operations of aseptic processing and/or isolator technology such as Diafiltration and Concentration of Proteins, Formulation of Proteins, Filling of Proteins in syringes and Vials within Isolators / Barrier Systems or in aseptic area process, Lyophilization process with Automatic Loading within Isolators / Barrier Systems or loading Lyophilizers on aseptic environment, Clean in Place (CIP) and Steam in Place (SIP) process in different systems, Decontamination of Isolator/ Barrier System with Vapor Hydrogen Peroxide (VHP), Sterilization cycles with Steam Autoclaves and Dry Heat Ovens and Tunnels, Isolators and gloves leak test.
* Operates in an efficient manner of the manufacturing processes to maximize product yield of products.
* Monitors critical process parameters and proactively takes necessary action to prevent process deviation and/or product losses.
* Maintains housekeeping within controls and aseptic environments, according to procedures.
* Handle Hazardous and Non-hazardous waste according to EHS procedures.
* Receives, verifies and maintains all production records and transaction documents error free and in compliance with established procedures including computer generate transactions.
* Receives, handle, verifies and weights excipients, drug substances, and/or active ingredients.
* Performs systems integrity test such as isolators, ultra filtration skid, distribution systems, filters and gloves as required.
* Verify calibration status of critical instruments before process operation.
* Complete production documen...
- Rate: Not Specified
- Location: Manati, US-PR
- Type: Permanent
- Industry: Engineering
- Recruiter: BMS
- Contact: Not Specified
- Email: to view click here
- Reference: R1605022
- Posted: 2026-10-07 09:05:26 -
- View all Jobs from BMS
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