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Helpdesk Technician II Summary We are seeking a Helpdesk Technician II who is customer-focused, collaborative, and technically strong. This role provides hands-on support for end users across the organization, resolves hardware, software, and access issues, and follows established procedures in a Gx

Manufacturing Specialist – Filling (2nd shift) SummaryINCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Manufacturing Specialist is a key technical role within

We are seeking a Senior Project Manager who has extensive experience managing projects in aseptic manufacturing, technology transfers, and/or new product launches of commercial products or large budget projects. Are you skilled in managing projects so that they are routinely delivered on time and wi

Are you an IT professional looking for an exciting opportunity with an organization where you can have an impact on global health and wellness? We are looking for a Senior ERP Systems Analyst who will help with our growing IT department. Do you naturally create new ways to deliver exceptional result

TSMS – Technical Transfer Engineer The Technical Services and Manufacturing Sciences (TSMS) Technical Transfer Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufactur

Join our dynamic Quality Assurance team as a QA Senior Specialist - Supplier Quality, where you'll play a critical role in maintaining the integrity of our supply chain and protecting product quality. This position offers the opportunity to work cross-functionally with Purchasing, Quality Operations

Process Specialist The Process Specialist is responsible for working directly with the operations team and is to work closely with the quality systems team to provide information and/or feedback for manufacturing deviation investigations and CAPA implementation. Additionally, the Process Specialist

The Senior Manager of Validation Engineering is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing and packaging facility. The ideal candidate has practical experience in qualification and validation as well as leadership experience. The Se

We are looking for an Engineering Technical Writer who is a detail-oriented documentation professional with a strong technical background and a thorough understanding of GMP documentation standards in a regulated pharmaceutical manufacturing environment. Embedded within INCOG BioPharma's Engineering

Job Description INCOG BioPharma Services is seeking an experienced and highly motivated Packaging Supervisor to lead second shift operations within the packaging department. This role is responsible for overseeing bulk and automated packaging activities for sterile drug products, ensuring safe, comp

Manager of Inspection Summary INCOG BioPharma is seeking a seasoned leader with extensive subject matter expertise in the inspection and packaging of sterile drug products. The primary purpose of this role is to provide strategic leadership, operational management, and technical excellence across ou

The Warehouse Associate is responsible for ensuring the accurate and efficient handling, storage, and distribution of GMP products within the warehouse. This role involves receiving, storing, picking, and packing GMP products while adhering to strict safety and regulatory standards. The warehouse as

Description INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation of inspection and packaging equipment. The Equipment Specialist has a key technical role within INCOG

Position Summary INCOG BioPharma Services, Inc. is seeking a dedicated and experienced Human Resources Manager to join our team as the primary off-shift HR partner at our Fishers, Indiana facility. This role will support a dynamic, Good Manufacturing Practices (“GMP”) regulated Contract Development

INCOG BioPharma is seeking a highly motivated Principal Validation Engineer with commissioning and qualification of sterile manufacturing systems, combination packaging, or automation, computer system, and software assurance expertise to join our team. The Principal Validation Engineer is a key indi

The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics and GMP manufacturing. The Manufacturing Specialist will be expected to work hands-on, be actively involved in continuous process impro

INCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding a

The Manufacturing Supervisor is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor support and review of MBR’s, providing coaching and feedback to operations team. Stra

We are looking for a QA Manager - Batch & Deviation Execution, who thrives on driving batch-impacting deviations to timely, high-quality closure. Are you the person who brings order, urgency, and technical rigor to complex cross-functional investigations? Does the idea of building a deviation manage

The Associate Director of Enterprise Systems serves as the enterprise system and process owner for a portfolio of mission‑critical Enterprise Systems within a GxP‑regulated Contract Development and Manufacturing Organization (CDMO). This role has end‑to‑end accountability for the strategy, governanc