Job Description. We are seeking an experienced Validation Specialist to support validation activities for Syringe Assembly Machines (SAM) in a GMP-compliant pharmaceutical environment. The ideal candidate will possess a strong understanding of the validation lifecycle and documentation required to ensure compliance with industry standards and regulations. Key Responsibilities. Perform validation activities for Syringe Assembly Machines, including...
Job Description. We are seeking an experienced Validation Specialist to support validation activities for Syringe Assembly Machines (SAM) in a GMP-compliant pharmaceutical environment. The ideal candidate will possess a strong understanding of the validation lifecycle and documentation required to ensure compliance with industry standards and regulations. Key Responsibilities. Perform validation activities for Syringe Assembly Machines, including...
Company Description. Assure Infusions is addressing the critical IV fluid supply chain challenges by building a cutting-edge automated facility in Central Florida. Our mission is to support the healthcare system by providing consistent access to essential medical products and a reliable. supply of IV fluids to hospitals and healthcare facilities. Assure Infusions is dedicated to innovation and operational excellence in the medical manufacturing f...
What You Will Do. GFT. is seeking a. Validation Specialis. t to join our Building and Places Group. This position can be based in. Eastern Pennsylvannia or Central New Jersey. This position requires a minimum of 3 days per week in-office or on-location, except during protocol execution periods which require 100% on-location effort. GFT office assignment location is negotiable. Client and OEM vendor sites vary per project, and the majority of work...
What You Will Do. GFT. is seeking a. Validation Specialis. t to join our Building and Places Group. This position can be based in. Eastern Pennsylvannia or Central New Jersey. This position requires a minimum of 3 days per week in-office or on-location, except during protocol execution periods which require 100% on-location effort. GFT office assignment location is negotiable. Client and OEM vendor sites vary per project, and the majority of work...
What You Will Do. GFT. is seeking a. Validation Specialis. t to join our Building and Places Group. This position can be based in. Eastern Pennsylvannia or Central New Jersey. This position requires a minimum of 3 days per week in-office or on-location, except during protocol execution periods which require 100% on-location effort. GFT office assignment location is negotiable. Client and OEM vendor sites vary per project, and the majority of work...
What You Will Do. GFT. is seeking a. Validation Specialis. t to join our Building and Places Group. This position can be based in. Eastern Pennsylvannia or Central New Jersey. This position requires a minimum of 3 days per week in-office or on-location, except during protocol execution periods which require 100% on-location effort. GFT office assignment location is negotiable. Client and OEM vendor sites vary per project, and the majority of work...
Job Details. Do you want to work with a company that tackles fascinating problems and find solutions to complex challenges. Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With an advanced manufacturing facility and expertise in influenza science we are one of the world leaders in the production of the influenza vaccine. We operate as one integrated global company, drawing together expert staff from different ...
Job Description. This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, FDA requirements and company policy. Development and execution of equipment and facilities validation protocols is the primary responsibility of this position. Inherent is the responsibility to ensure the accuracy and completeness of each validation study and that each study is ac...
Job Description. This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, FDA requirements and company policy. Development and execution of equipment and facilities validation protocols is the primary responsibility of this position. Inherent is the responsibility to ensure the accuracy and completeness of each validation study and that each study is ac...
Do you want to work with a company that tackles fascinating problems and find solutions to complex challenges. Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With an advanced manufacturing facility and expertise in influenza science we are one of the world leaders in the production of the influenza vaccine. We operate as one integrated global company, drawing together expert staff from different countries to ...
