About Site Catalent’s Greendale, Indiana site is a key part of the company’s Wellness business, serving as one of North America’s primary gummy development and manufacturing centers. The site specializes in the formulation and production of
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Job Description JOB DESCRIPTION & SPECIFIC OBJECTIVES The Senior (Sr) Specialist, Change Control and Deviation Management role will be involved in implementation and maintenance of Change Control and Deviation Management procedures at our Companys Wilmington Biotech. The Sr
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Deviations Investigation Specialist partners with Operations, Quality, and cross-functional teams
We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves
About Site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility
QA Compliance Specialist Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification, initiation in EtQ and closure. Support external client review and resolution of
Deviations Specialist The Deviations Specialist supports the Badger Mission and Principles as a member of the Quality Unit. They are responsible day-to-day administration and coordination of the deviation management workflow within the QMS, under QA Supervisor direction. They also
Deviations and Investigations Technical Writer Scope: Writing documents for deviations and investigations; paper records 5+ years of technical writing experience required 10 week contract opportunity with possibility of extension Onsite location in Philadelphia, PA...
Indianapolis, INDescription Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Verista in Indianapolis is seeking a CQV Engineer to support change control and deviation management within a regulated cGMP environment. You will collaborate with cross-functional teams to ensure changes are properly assessed, documented, and executed, with hands-on
An established industry player is seeking a Quality Assurance Specialist to enhance cGMP quality operations at their Bothell facility. This role is pivotal in managing deviations, conducting investigations, and ensuring compliance with regulatory standards. The ideal candidate
CVS Health in the United States is seeking a Senior Manager to lead Medical & Pre-Payment Policy deviation management. You will oversee governance, interpretation of policies, and audit-ready documentation, collaborating with Product, Plan Sponsor, Provider Network, Clinical,
Amgen Inc. (IR) seeks a Senior Manager of Quality Assurance for the Major Deviations Lifecycle team to lead investigations, CAPAs, and risk assessments across manufacturing, packaging, and QA operations. The role ensures timely, compliant handling of significant
Verista is seeking an entry-level Deviation Investigator / CQV Engineer in the Pharma sector. Based in Indianapolis, IN, you will be trained on Deviation Investigation as part of a growing team focused on enabling life sciences clients to
Amgen seeks a Manager for Manufacturing Environmental & Contamination Control in West Greenwich. In this role, you will oversee deviation management and ensure compliance in manufacturing operations. Your responsibilities include managing deviation owners, leading investigations, and implementing continuous
Senior Manager Quality Assurance – Major Deviations Lifecycle TeamSkip to main content#Senior Manager Quality Assurance – Major Deviations Lifecycle Team page is loaded# Senior Manager Quality Assurance – Major Deviations Lifecycle TeamApplyremote type: On Sitelocations: US - Puerto Rico
We are seeking a CQV Engineer to support change control and deviation management activities. This role will play a critical part in maintaining compliance, supporting quality systems, and ensuring manufacturing changes are properly assessed, documented, and executed
Amgen is seeking an Engineer for F&E Environmental & Contamination Control. This vital role involves managing equipment deviations, conducting technical investigations, and ensuring compliance with regulatory standards. The successful candidate will collaborate across various functions, develop corrective