- PCI Pharma Services (Philadelphia, PA)
- …network to pioneer and shape the future of PCI. **Summary of Objective:** Validation / Sterilization Manager is responsible for qualification, validation , ... for protocol execution. + Collaborates with the site commercial Validation Manager for any validation ...process experience.. + 5 years of experience in terminal sterilization validation and sterility assurance… more
- Integra LifeSciences (Mansfield, MA)
- …changes. + Provides guidance and input on the resolution of sterility related non-conformances + Supports sterilization validations, cleaning validations, ... DUTIES AND RESPONSIBILITIES + Serves as a Subject Matter Expert for Sterilization across the company. + Maintains and revises procedures and methodologies to… more
- Pfizer (Rochester, MI)
- …for managing a team of Compliance, QA Documentation, Supplier Management, Validation , Sterility Assurance, Combination Product Quality, and Data Integrity ... of quality responsibilities including; Compliance, QA Documentation, Supplier Management, Validation , Sterility Assurance, Combination Product Quality, and Data… more
- Integra LifeSciences (Plainsboro, NJ)
- …monitoring * Bioburden test method validation and monitoring * Radiation sterilization validation and dose audit management * Ethylene oxide sterilization ... validation and requalification * Reprocessible device cleaning and sterilization validation **ESSENTIAL DUTIES AND RESPONSIBILITIES** To perform this job… more
- Integra LifeSciences (Anasco, PR)
- …method validation and monitoring * Reusable Medical Devices * Radiation sterilization validation and dose audit management * Ethylene oxide sterilization ... validation and requalification * Reprocessible device cleaning and sterilization validation **ESSENTIAL DUTIES AND RESPONSIBILITIES** To perform this job… more
- Integra LifeSciences (Cordova, TN)
- …* Bioburden test method validation and monitoring * Radiation sterilization validation and dose audit management **SUPERVISION RECEIVED** Under direct ... endotoxin test method validation and monitoring, Bioburden test method validation and monitoring, and radiation sterilization and dose audit management… more
- Integra LifeSciences (Columbia, MD)
- …+ Bioburden test method validation and monitoring + Radiation sterilization validation and dose audit management **SUPERVISION RECEIVED** Under direct ... endotoxin test method validation and monitoring, Bioburden test method validation and monitoring, and radiation sterilization and dose audit management… more
- ATS Automation (Indianapolis, IN)
- …synthesis and dispensing modules for vials and syringes, LAF shielded isolators, sterility testing isolators, VPHP generators for sterilization , solid target ... 46250 Date: Feb 27, 2025 Site Leader - Project Manager The Site Leader - Project Manager ...for managing project commitments for installation, commissioning, SAT, and validation of larger Comecer projects in North America. This… more
- Saint-Gobain (Beaverton, MI)
- …+ Ensure adequate training program is in place. + Oversight of applicable Validation Master Plan including equipment, process, product, sterilization , and test ... **Plant Quality Manager - Manufacturing, Life Sciences; Beaverton, MI** If...and Supply Chain. + Oversight and Maintenance of Site Sterility Program + Customer Management including facilitating/hosting customer audits,… more
- BD (Becton, Dickinson and Company) (Sumter, SC)
- …changes. + Sterilization - proper expertise is available to manage sterilization activities and product meets sterility claims. + Environmental Monitoring - ... comply with currently approved procedures and with FDA/GMP/ISO guidelines. + Validation - new processes and process changes, including process, molding, software,… more
- ADM (Kennesaw, GA)
- …SCOPE** The Fermentation Technician will work, under minimal supervision of the Production Manager , on the production of microorganisms. They will work in a hands-on ... from start-up to shutdown, including media and buffer preparation, equipment sterilization , microbial growth, recovery, filtration, and drying. + Ensure work is… more
- Contract Pharmacal Corp (Hauppauge, NY)
- …use, cGMP, GDP, data integrity, DEA requirements, etc. + Media preparation, sterilization , storage, growth promotion and sterility tests. + Use scientific ... of commercial materials (raw materials, finished product release, stability, validation , investigation), and environmental samples, as assigned, and documenting… more