Facilities Maintenance

Open Positions

Maintenance Associate I – Indianapolis, IN

Associate I, Maintenance 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 the cGxP (Current Good Practices), Quality Assurance, and Company SOPs (Standard Operating Procedure) standards at our state-of-the-art facility.

Project Coordinator – Indianapolis, IN

The 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.

Coming Soon

Maintenance Associate I – Columbus, IN

The 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, IN

The 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, IN

The 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 Filled

Validation Associate I – Indianapolis, IN

The 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, IN

The 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.