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Catalent Pharma Solutions jobs

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

Catalent Pharma Solutions  22 days ago
Verista jobs

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  21 days ago
MSD jobs

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

MSD  14 days ago
Kindeva Drug Delivery jobs

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

Kindeva Drug Delivery  14 days ago
CVS Health jobs

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

CVS Health  13 days ago
Catalent Pharma Solutions jobs

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

Catalent Pharma Solutions  4 days ago
KBI Biopharma jobs

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

KBI Biopharma  18 days ago

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

W.S. Badger Company, Inc.  5 days ago
ProPharma jobs

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...

ProPharma  4 days ago

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

Verista, Inc.  12 hours ago

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

Socket.dev  10 hours ago

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

Verista  10 hours ago

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

TechDigital Group  10 hours ago
CVS Health jobs

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,

CVS Health  10 hours ago
Amgen Inc. (IR) jobs

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

Amgen Inc. (IR)  10 hours ago

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

Veristainc  10 hours ago
Amgen jobs

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

Amgen  10 hours ago
Amgen Inc. (IR) jobs

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

Amgen Inc. (IR)  11 hours ago

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

Veristainc  11 hours ago
Amgen jobs

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

Amgen  11 hours ago

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