When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,
Specialist I - Quality Assurance Systems, Deviations/CAPAs Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities.
CAPA Manager Bloomington, Indiana, United States Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US
Systems Manager II- CAPA The position is responsible for administrative oversight of the university-wide course approval process system (CAPA) and the Public CV and Syllabus System, including providing guidance and responding to inquiries and technical help requests from
Manager, Global CapA System CooperSurgical is a leading fertility and womens healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. As a division
CAPA Process Analyst II Our client, a leading organization in the healthcare and medical device industry, is seeking a passionate and detail-oriented CAPA Process Analyst II to join their team. As a CAPA Process Analyst II, you will be
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
Plant CapA Investigation Leader Fairfield, CA EXP 2-5 yrs DEG Bach RELO BONUS Job Description. The primary responsibilities of the CAPA Coordinator are multifunctional and include management of the plant Exception Report and Corrective action/Preventative Action (CAPA) program, Customer
Process Change & CAPA Lead At Elanco it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals
Capa General Manager Four Seasons is powered by our people. We are a collective of individuals who crave to become better, to push ourselves to new heights and to treat each other as we wish to be
FDA Audit Readiness Lead Lead FDA audit and inspection readiness activities across the business. Own and present CAPA effectiveness, investigation quality, risk assessments, and HHE processes during FDA interactions. Act as the primary presenter/interface for FDA inspections,
Manager Of The Arden Hills Based Cardiac Rhythm Management And Diagnostics (CRMDx) Field CAPA Team At Boston Scientific, well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing
Sr. Specialist Ready to transform complex manufacturing anomalies into flawless, inspection-ready narratives? As a Sr. Specialist, youll dive into the heart of GMP operations-spearheading high-impact deviation investigations, mastering root cause analysis, and orchestrating cross-functional compliance excellence.
CAPA Specialist At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patients mobility is enhanced by a Zimmer Biomet
CAPA Manager The CAPA Manager plays a pivotal role in ensuring that organizational CAPA initiatives are executed with the highest standards of quality and efficiency within the sterile pharmaceutical manufacturing environment. This position is responsible for developing, implementing, and
CAPA Specialist The CAPA Specialist is responsible for driving the effective closure of Corrective and Preventive Actions (CAPAs) associated with deviations, investigations, and non-conformances within pharmaceutical packaging and aseptic filling operations. This role ensures that all activities comply with
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Job Description The Engineer III, Manufacturing Engineering, at Thermo Fisher Scientific will
JOB QUALIFICATIONS: Bachelor’s Degree within Engineering A minimum of 4 years progressive experience in a related field Experience supporting a QMS in accordance with the latest ISO 9001 standard. Experience in process design using in-process controls
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes