2,094 capa jobs at 1,080 companies in United States
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CAPA Lead
El Paso, Texas, United States
OnsiteFull Time
BDNYSE: BDX: Manufactures medical devices, surgical instruments, and pharmacy automation systems.
5+ YOE2+ Mgmt5+ years quality/manufacturing experience in regulated industry, 2+ years CAPA/investigations leadership, bachelor’s in engineering/quality, FDA/GMP knowledge, bilingual English/Spanish.
StrykerNYSE: SYK: Manufactures medical devices and equipment for healthcare providers.
4+ YOE4+ years CAPA/quality systems experience in a regulated industry, QMS and CAPA expertise, project and stakeholder management, audit and regulatory interaction experience.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, eCAPA
Zimmer BiometNYSE: ZBH: Manufactures orthopedic implants and robotic surgical systems.
2+ YOE2+ years related experience (medical device preferred); CAPA management, QMS auditing, familiarity with 21 CFR 820 and ISO 13485; basic MS Office skills; strong problem-solving and collaboration skills.
ELYON International: IT consulting firm providing digital modernization and data solutions.
3+ YOEExperienced CAPA quality engineer with 3+ years (Master) or 5+ years (Bachelor) in CAPA, root cause analysis, project management; knowledge of 21 CFR Parts 803, 806, 820; ISO 13485/9001/14971; strong communication.
AbbottNYSE: ABT: Manufactures medical devices, diagnostics, and nutritional health products.
4+ YOEBachelor’s degree required; 4+ years QA in GMP; master’s preferred; knowledge of infant formula/regulatory requirements; strong communication and cross-functional collaboration.
GMP, CAPA, Root cause analysis, Investigations, Quality systems
Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
5+ YOE3+ MgmtBachelor's degree,5+ years pharma/biotech/medical device manufacturing experience,3+ years QA leadership,expertise in CAPA,investigations,root cause analysis and QRM,knowledge of FDA/EU/ICH requirements.
Corrective and Preventive Action (CAPA) Coordinator
Carrollton, Texas, United States
OnsiteFull Time
INW: Manufactures and formulates nutritional supplements for global brands.
2+ YOE2+ years QA/CAPA experience in regulated industries; administer CAPA system, perform root cause analysis (5 Whys, Fishbone, FTA, FMEA), use eQMS, support audits. Bachelor's degree preferred.
Electronic Quality Management Systems (eQMS), 5 Whys, Fishbone (Ishikawa) Diagrams, Fault Tree Analysis, FMEA
AbbottNYSE: ABT: Provides medical devices, diagnostics, and science-based nutritional products.
4+ YOEBachelor’s degree required in Business, Science, Engineering, Math/Statistics, or related field. 4+ years QA in GMP-regulated industry; knowledge of infant formula and medical nutrition regulatory requirements; strong communication; ability to manage multiple projects.
GMP, CAPA, root cause analysis, investigation, statistical applications
CooperSurgicalNasdaq: COO: Manufactures medical devices for fertility and women's health.
8+ YOE5+ Mgmt8+ years in quality within regulated industry; 3-5 years CAPA management; 5+ years QA leadership; strong regulatory and CAPA knowledge; English required, Spanish preferred.
PhilipsEuronext Amsterdam: PHIA: Manufactures medical imaging systems and personal care appliances.
5+ YOE5+ years driving process excellence in regulated environments, CAPA expertise, strong communication, MS Office and Planisware/Clarity/QlikView/Windchill/SAP experience, Bachelor's/Master's or equivalent experience.
Boston ScientificNYSE: BSX: Developing and manufacturing innovative medical devices for less-invasive treatments.
7+ YOEBachelor's degree and 7+ years supporting nonconforming events and CAPA in regulated environments; experience with FDA/ISO/MDR, strong communication, problem solving, and mentoring skills.
McKessonNew York Stock Exchange: MCK: Distributes pharmaceuticals and provides healthcare information technology solutions.
13+ YOE6+ MgmtBachelor's in life sciences/engineering or equivalent, 13+ years quality experience in regulated pharma/healthcare, 6+ years people management, deep knowledge of FDA/DEA/regulatory requirements, expertise in investigations/CAPA/recalls.
Siemens HealthineersFrankfurt Stock Exchange: SHL: Provides medical imaging and diagnostic solutions to healthcare providers.
2+ YOEManage CAPA program, perform root cause analysis, maintain CAPA/QMS documentation per ISO 13485/21 CFR Part 820, use quality tools and QMS software, and support audits (requires bachelor's and 2+ years quality experience).
Siemens HealthineersFrankfurt Stock Exchange: SHL: Manufactures medical imaging and laboratory diagnostic equipment.
2+ YOEBachelor's in engineering or related field, 2+ years quality engineering experience, CAPA program management, familiarity with ISO 13485/21 CFR Part 820, QMS software, root cause analysis and audit participation.
CATSweb, MasterControl, TrackWise, Electronic Quality Management System (QMS)
Boston ScientificNYSE: BSX: Manufacturer of interventional medical devices and technologies.
7+ YOEBachelor's degree and minimum 7 years supporting CAPA/nonconforming events in regulated industries; CAPA mentorship, problem-solving, communication, and attention to detail required.
Boston ScientificNYSE: BSX: Developer and manufacturer of innovative medical devices and therapies.
7+ YOE7+ years supporting nonconforming events and CAPA in regulated environments; bachelor\u0000s degree; CAPA mentorship, structured problem-solving, strong communication and attention to detail.
American RegentTokyo Stock Exchange: 4568: Manufactures injectable pharmaceutical products for human and veterinary use.
5+ YOEBachelor's in science/engineering,5+ years QA experience in regulated environment,knowledge of FDA regulations,CAPA writing and risk management,strong analytical and organizational skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
GetingeNasdaq Stockholm: GETI B: Manufactures medical equipment for acute care and life sciences.
5+ YOEBachelor's in engineering or science required, 5+ years managing CAPA processes, proficiency with TrackWise, Minitab and Microsoft Office, knowledge of ISO 13485 and FDA 21 CFR Part 820, strong root-cause analysis and auditing skills.
TrackWise, Minitab, Microsoft Word, Microsoft Excel, Microsoft PowerPoint