What are the responsibilities and job description for the GMP Manufacturing Technician III position at Orano USA?
Orano Med Theranostics
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.
Orano Med Theranostics
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off., Orano Med Theranostics
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off., Orano Med Theranostics
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.
Orano Med Theranostics
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off., Orano Med Theranostics
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off., Orano Med Theranostics
Orano Med is seeking a detail-oriented GMP Manufacturing Technician III
We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite.
Key Responsibilities
Follow written procedures for non-clinical manufacturing
Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines
Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product
Follow and adhere to production schedules and timelines
Execute room and equipment preparation for manufacturing operations
Perform room sanitization activities as needed to maintain controlled environment conditions
Participate in isolator and room monitoring
Participate in room and isolator preparation for manufacturing
Stocking materials in the GMP labs
Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team
Identify process errors and report to supervisor
Participate in deviation investigations and follow management guidance for corrective and preventive actions
Clean, sanitize and sterilize equipment and components to support production operations
Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs.
Demonstrate ability to perform tasks with minimal guidance once trained
Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing
Complete on the job training for cleaning, gowning, GMP suite access, and equipment
Primary operator for release testing of cold vials/syringes and solutions
Monitoring of materials stock, requesting orders, obtaining relevant documents and submitting for release
Assist in troubleshooting process errors
Suggest corrective actions in support of deviation investigations
Assist in editing non-clinical process & equipment documents
Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.
