Deviation Management Jobs In Pendleton, Indiana - 50 Job Positions Available

Senior Quality Control Compliance Specialist Summary The Senior Quality Control Compliance Specialist plays a vital role on the QC team with analytical and microbiological testing experience. This role will support laboratory processing of finished product, incoming

The QC Microbiology Technician will work closely with QC Microbiologists and the QC Microbiology Manager to support development and readiness activities for the Quality Control Microbiology lab. The QC Microbiology Technician will perform routine sampling for

The Process Specialist is responsible for working directly with the operations team and providing support by identifying potential process improvements and procedural gaps. As well as performing processes improvements to address procedural gaps and champion process

Working closely with the QA Supervisor, the QA Associate will be instrumental in ensuring site compliance with Regulations, ISO Standards, organizations SOPs as well as support in championing and developing organization’s Quality Mindset, as well as

Working closely with the QA Supervisor, the QA Associate will be instrumental in ensuring site compliance with Regulations, ISO Standards, organizations SOPs as well as support in championing and developing organization’s Quality Mindset, as well as

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,

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Working closely with the QA Batch Manager, the Senior QA Batch Specialist will be instrumental in supporting major QA programs related to batch review, disposition and continuous improvement. They will also be key in championing and

Senior Manager of Reliability Summary INCOG BioPharma is seeking an experienced and results-oriented reliability leader to serve as the Senior Manager of Reliability. This role is responsible for building, leading, and managing the equipment reliability function

Working closely with the QA Supervisor, the QA Associate will be instrumental in ensuring site compliance with Regulations, ISO Standards, organizations SOPs as well as support in championing and developing organization’s Quality Mindset, as well as

We are looking for a Validation 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

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

GxP Training Facilitation Specialist Summary INCOG is seeking a highly skilled GxP Training Facilitation Specialist to deliver and execute comprehensive training programs across INCOG operations. This role is critical to ensuring that all personnel possess the

Summary INCOG is seeking a highly capable GxP Training Supervisor to lead and coordinate the day-to-day activities of the sites Manufacturing Training Specialists. This role is accountable for ensuring that training delivery, competency assessment, curriculum administration,

Working closely with the QA Supervisor, the QA Specialist – Batch Review will be instrumental in supporting major QA programs. They will also be key in championing and developing the organization’s Quality Mindset, and culture of