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
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
Deviation Investigation Writer - Viral Vector Location: This is an on-site position located in Houston, TX. Available shift: Monday through Friday, standard office hours (approximately 8:00 a.m. to 5:00 p.m.) The Deviation Investigator III – Viral Vector is
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...
Amgen is seeking an Engineer in F&E Environmental & Contamination Control to lead deviation investigations and ensure quality system compliance. You will report to Facilities & Engineering and own end-to-end documentation, investigations, RCA, and CAPA activities. You
Madrigal, located in Conshohocken, is a biopharmaceutical company seeking a Quality Assurance professional to focus on deviation management for metabolic dysfunction treatments. The role involves leading investigations, ensuring compliance, and maintaining inspection readiness. The ideal candidate will
Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980,
Amgen Thousand Oaks is seeking a Specialist Manufacturing to investigate deviations across manufacturing, QA, and supply chain, determining scope, root cause, and effective CAPAs. You will collaborate with cross‑functional teams to ensure regulatory alignment and robust documentation.
An established industry player is seeking a Deviation Investigator to join their Manufacturing Sciences and Technology team. This role is pivotal in ensuring quality compliance by investigating deviations and managing corrective actions. The ideal candidate will leverage their
Deviation Supervisor Work Schedule: Standard (Mon-Fri) Environmental Conditions: Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description:
Amgen is seeking an Engineer for F&E Environmental & Contamination Control in West Greenwich, RI. The role involves managing technical deviations, ensuring compliance through rigorous documentation, and collaborating with multiple departments to enhance operational excellence. The ideal
Amgen seeks a Sr Mgr Quality Assurance to lead the Major Deviations Lifecycle Team across manufacturing, packaging, lab and support operations. You will drive investigations, CAPAs, and regulatory readiness, partnering with QA, QC, Manufacturing, Regulatory Affairs and
Madrigalpharma is seeking a Senior Manager for Deviation Management within Quality Assurance in Conshohocken, PA. This role will be pivotal in managing deviation governance, ensuring compliance, and leading investigations related to quality assurance. Candidates should have a strong
Amgen is seeking a Senior Manager of Quality Assurance to lead the Major Deviations Lifecycle Team, ensuring timely, compliant investigations and CAPAs across manufacturing, packaging, laboratory, and support operations. The role partners with QA, QC, Manufacturing, Engineering,
Johnson Service Group, Inc. is recruiting Deviation Specialists in the United States. You will support deviation management by assessing product impacts, identifying root causes, and implementing corrective actions. You will author and update GMP documentation and collaborate with