- CBRE (Indianapolis, IN)
- Quality & Compliance Specialist ( FDA Regulated Industry) Job ID 244368 Posted 22-Oct-2025 Service line GWS Segment Role type Full-time Areas of Interest ... highly-regulated spaces within the industry. About the role As a CBRE Quality and Compliance Analyst, you will assist in the maintenance of services provided to… more
- Catalent Pharma Solutions (Greendale, IN)
- …Food Safety Plan (HACCP), Food Quality Plan (FQP) standards. Responsible for ensuring compliance to FDA and cGMP standards for Quality Control, including ... ** Quality Specialist I** **Position Summary** Catalent,...issues that need attention. + Document all areas of non- compliance and ensure corrective action to eliminate them. +… more
- Cardinal Health (Indianapolis, IN)
- …and procedures and ensures that all products and services are properly reviewed for quality and documented. **_What a Principal Specialist , Quality Assurance ... QA Principal Specialist is responsible for ensuring quality standards and procedures are followed and will oversee...Assists in the release of the final product in compliance with applicable regulations ( FDA , EU, etc.)… more
- Cardinal Health (Indianapolis, IN)
- …to making a difference for our customers and communities. **What a Senior Specialist , Quality Control (Chemistry) contributes to Cardinal Health** Quality ... set and/or development goals and business needs. + Champion Quality , cGMP compliance , and EHS/Radiation Safety practices....experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device) preferred. +… more
- Bristol Myers Squibb (Indianapolis, IN)
- …The Senior Specialist , QA Operations will help support operations through quality oversight in a Radiopharmaceutical facility in Indianapolis, IN. The Senior QA ... responsible for material and batch disposition activities. This position will utilize quality assurance knowledge in ensuring compliance in operations to support… more
- CBRE (Jeffersonville, IN)
- …those respective contract terms. **ESSENTIAL DUTIES AND RESPONSIBILITIES** Oversees the day-to-day Quality and Compliance Team operations at one account sites ... as defined in the master service agreement (MSA) or Quality Agreement. Executes the CBRE compliance program...preferred. Previous supervisory experience a plus. **CERTIFICATES and/or LICENSES** FDA , ISO, or similar quality assurance audit… more
- Bristol Myers Squibb (Indianapolis, IN)
- …RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Quality Assurance Incoming Material Disposition Senior Specialist is responsible ... and global current Good Manufacturing Practice (cGMP). The Senior Specialist provides Quality support and oversight for...is preferred + Minimum of 5 years' experience in quality assurance and/or compliance roles in the… more
- Stryker (Indianapolis, IN)
- Stryker is seeking a **Staff Specialist , Post Market Surveillance** for our Medical division. This is a remote role with preference for someone located in the ... Central Time Zone. As the **Staff Specialist , Post Market Surveillance** , you will play a...role in protecting patients and supporting innovation by driving compliance across global markets. **What You Will Do** +… more
- Stryker (Columbia City, IN)
- Stryker is hiring a **Staff Specialist , Regulatory Affairs** , ( **Hybrid** ) to join our Regulatory Affairs team in **Columbia City, Indiana** . This individual ... and extremities products. + Evaluate regulatory environments and advise on compliance throughout the product lifecycle. + Anticipate regulatory obstacles and develop… more
- Lilly (Indianapolis, IN)
- …activities of the medical team (and direct reports, if applicable) are in compliance with current local and international regulations, laws, guidance (for example, ... FDA , ICH, and CPMP etc.), Good Clinical Practices (GCPs),...Practices (GCPs), company standards, Lilly policies and procedures, global quality standards, the Principles of Medical Research and activities… more