Coming SoonMaintenance Associate I – Columbus, INThe Maintenance Associate I is a crucial member of the Sentry BioPharma Services team, responsible for ensuring the facility and grounds are maintained to the highest standards of cleanliness, safety, and efficiency. This role is essential in maintaining cGxP (Current Good Practices), Quality Assurance, and Company SOPs (Standard Operating Procedure) standards at our state-of-the-art facility. |
Maintenance Associate II – Indianapolis, INThe Maintenance Associate II is a crucial member of the Sentry BioPharma Services team, responsible for ensuring the facility and grounds are maintained to the highest standards of cleanliness, safety, and efficiency. This role is essential in maintaining cGxP (Current Good Practices), Quality Assurance, and Company SOPs (Standard Operating Procedure) standards at our state-of-the-art facility. |
Validation Associate I – Columbus, INThe Validation Associate I will execute approved validation protocols, such as Installation Qualifications (IQ), Operational Qualifications (OQ) and Performance Qualifications (PQ) and participate in generation of validation/qualification reports. The position will also provide support and troubleshooting for all validated/qualified equipment as well as identify process improvements. Projects and duties will be completed in compliance with applicable cGMP, FDA, and all other applicable regulatory requirements. |
Recently FilledValidation Associate I – Indianapolis, INThe Validation Associate I will execute approved validation protocols, such as Installation Qualifications (IQ), Operational Qualifications (OQ) and Performance Qualifications (PQ) and participate in generation of validation/qualification reports. The position will also provide support and troubleshooting for all validated/qualified equipment as well as identify process improvements. Projects and duties will be completed in compliance with applicable cGMP, FDA, and all other applicable regulatory requirements. |
Validation Coordinator – Indianapolis, INThe Validation Coordinator will be responsible for overseeing all aspects of validation activities within Sentry’s state-of-the-art GMP facility, ensuring compliance with regulatory requirements and internal procedures. Responsibilities may include creating, reviewing, and executing validation protocols, such as Installation Qualifications (IQ), Operational Qualifications (OQ) and Performance Qualifications (PQ) and generation of validation/qualification reports. The position will also provide support and troubleshooting for all validated/qualified equipment as well as identify process improvements. Projects and duties will be completed in compliance with applicable cGMP, FDA, and all other applicable regulatory requirements. |
Project Coordinator – Indianapolis, INThe Project Coordinator, Facilities will be responsible for supporting stakeholders with the planning, execution, and successful completion of various projects at Sentry’s state-of-the-art GMP facility, ensuring compliance with regulatory requirements and internal procedures. Responsibilities may include organizing and providing support for various parts of a project to ensure its success. This includes assigning and monitoring daily tasks and communication, as well as creating reports and updates for the Associate Director, Facilities, and other members of the project team. Projects and duties will be completed in compliance with applicable cGMP, FDA, and all other applicable regulatory requirements. |
Validation and Calibration Supervisor – Indianapolis, INThe Supervisor, Validation and Calibration will be responsible for overseeing and implementing validation activities to ensure compliance with current regulatory requirements and industry standards. This position leads, directs, and coordinates validation activities in accordance with the Company’s procedures, policies, goals, and objectives. As the company expands, the Supervisor will establish and guide a team of validation professionals to address the current and future requirements of the Company and its Clients. Projects and duties will be completed in compliance with applicable cGMP, FDA, and all other applicable regulatory requirements. |
Maintenance Associate I – Indianapolis, INThe Maintenance Associate I is a crucial member of the Sentry BioPharma Services team, responsible for ensuring the facility and grounds are maintained to the highest standards of cleanliness, safety, and efficiency. This role is essential in maintaining cGxP (Current Good Practices), Quality Assurance, and Company SOPs (Standard Operating Procedure) standards at our state-of-the-art facility. |