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- ...of relevant experience. Nice to Have Project Management Certification (PMP) preferred. Risk management and data-driven Quality management... ...insulin delivery devices. Regulatory compliance knowledge ISO Regulation and Medical Devices Regulations. Strong project...SuggestedTemporary workStart working todayLive inWork at officeLocal areaWorldwideFlexible hours
- ...The Lab Transformation Specialist supports compliance with GLP, ISO 17025, and other applicable standards, drives standardization... ...Master's Degree in Project Management or similar field, and/or PMP certification. Technical skills Lean or Six Sigma certification (Green...SuggestedWork experience placementLocal areaRelocation
- ...Business continuity/cyber resilience Familiarity with NIST, ISO 27001, CIS Controls, COBIT, or equivalent frameworks.... ...Risk, Compliance, Audit, Legal, and executive stakeholders. Certifications such as CISSP, CISM, CISA, CRISC, CCSP are advantageous. #J-...Suggested
- ...manufacturing processes. Ensure compliance with safety policies, GMP, ISO standards, and applicable regulations. Participate in... ..., Electrical Engineering, Science, or a related field. Certifications in Quality Assurance, Lean Manufacturing, or Six Sigma are...SuggestedWork at office
$58.1k
...maintain compliance with regulatory requirements, support the ISO 14001 EMS, and fulfill Corporate reporting and information needs... ...broader EHS management systems is preferred. Professional certifications related to Environmental Compliance, EHS, Sustainability, OSHA...SuggestedHourly payLocal areaShift work- ...with recognized security frameworks and standards such as NIST, ISO 27001, CIS Controls, COBIT, or equivalent. Strong... ...skills. Relevant bachelor's degree; Master's degree and certifications such as CISSP, CISM, CRISC, CISA, CCSP or equivalent are advantageous...Suggested
- ...Engineering, or related field preferred. Experience in FDA/ISO-regulated manufacturing environments, including GMP compliance,... ...continuous improvement, and critical-thinking skills; Lean Six Sigma certification and automation/programming experience are preferred....SuggestedLocal areaShift workDay shiftAfternoon shift
$11 per hour
...Operador también participa en la evaluación y solución de problemas del equipo según sea necesario, cumpliendo con las regulaciones de QSR, ISO, seguridad y medio ambiente. Responsabilidades # Seguir los procedimientos aprobados para poner en marcha el equipo y monitorear...SuggestedShift work- ...location and stakeholder base. Preferred Experience ~ Familiarity with regulated environments and quality frameworks (e.g., cGMP, ISO). Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at...SuggestedFull timeInternshipH1bLocal area
Johnson & Johnson
Puerto Rico2 days ago - ...relevant quality experience Advanced knowledge of GMP, FDA, ISO 13485, and Quality System Regulations Experience leading complex... ...and trend analysis Lean Six Sigma Green Belt or Black Belt certification Knowledge of manufacturing process controls and process...Suggested
- ...PhD) Lean Manufacturing and Six Sigma Green Belt or Black Belt certification Advanced statistical analysis expertise (DOE, SPC, MSA,... ...validation leadership (IQ/OQ/PQ) Regulatory knowledge of FDA QSR, ISO 13485, and GMP requirements Experience with automation,...Suggested
- ...on facility-related initiatives. Ensuring compliance with environmental, health, safety, and occupational regulations, including ISO 14001 and applicable company policies. Performing additional duties and special projects as assigned. Qualifications / Requirements...SuggestedFull timeInternshipH1bWork at officeLocal area
Johnson & Johnson
Puerto Rico19 hours ago - ...enterprise security, privacy, and regulatory requirements (NIST AI RMF, ISO/IEC 42001, SOC 2, PCI, and applicable retail/data-privacy... ...a plus. Preferred Qualifications CSPO/CSM or equivalent Agile certification. Security certifications (CISSP, CISM, or Security+) or AI...SuggestedContract workRemote work
$166.75k - $228.85k
...procedures across manufacturing sites Represent microbiology in internal and external audits including FDA inspections and ISO certifications Create long-term strategies and provide leadership direction to ensure quality, compliance, and business objectives...Suggested$58.1k
...maintain compliance with regulatory requirements, support the ISO 14001 EMS, and fulfill Corporate reporting and information needs... ...and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC...SuggestedHourly payLocal areaShift work- ...project execution, quality improvements, data analysis, and implementation of engineering solutions while ensuring compliance with GMP, ISO, safety, and regulatory requirements. You Will Be Responsible For Supporting and executing engineering projects of low to...Full timeInternshipH1bLocal area
Johnson & Johnson
Puerto Rico3 days ago - ...s platform architecture and cloud infrastructure (GCP). Ensure high availability, reliability, and audit‑ready compliance (SOC 2, ISO 27001). Partner with Product, Operations, and Compliance leaders to align technical solutions with client impact. Report directly...Full timeWork at officeLocal area
- ...Maintenance Management Systems) Ability to read and interpret technical documents, schematics and equipment manuals. Knowledge of ISO 9001, OSHA, IPC-A-610 or other regulatory standards. Administrative Skills: Document Control: Strong skills in Microsoft Office...Work at office
- ...soporte necesario para mantener y/o mejorar el rendimiento, la fiabilidad y la seguridad del servidor y la red en línea con BS 7799 / ISO 27001 y las mejores prácticas. Proporciona soporte para probar planes de DR y ayuda en los procedimientos de recuperación cuando...Work at office
Genera PR LLC
Puerto Rico10 days ago - ...with tool and machine design ~ Fluent in English and Spanish with strong written and oral communication ~ Knowledge of cGMP, OSHA, ISO 9000, and continuous improvement techniques ~ Expertise in packaging methods: heat sealing, thermoforming, thermoplastic ~ Strong...
- ...background in field corrective actions, CAPA, or product quality management. ~ Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, EU MDR, and other relevant medical device regulations. Proven experience leading FCA and CAPA processes, ideally within a...Work at officeLocal areaShift workDay shift
$16.83 - $23.56 per hour
...instrumentation techniques Ability to work with different hand tools and power tools. Demonstrated knowledge of FDA, OSHA, EPA and ISO regulations and standards. Ability to communicate and read in English and Spanish. Ability to self-taught in the use of...Hourly payTemporary workWork at officeShift workNight shiftWeekend workDay shift$17 per hour
...produccin conforme a las especificaciones de las Buenas Prcticas de Manufactura (cGMP). Ajusta la maquinaria de todos los equipos siguiente las especificaciones y regulaciones de la compaa. Cumple con las normas QSR, ISO, de seguridad y medioambientales. Advance ServicesShift work- ...environmental monitoring trending and interpretation of microbiological and particulate data. Knowledge of relevant standards, such as ISO 14644, ISO 11137, ISO 11737 and EN 17141, and experience with quality systems including corrective and preventive action, change...
- ...design reviews, and oversee new equipment installations. --Ensure compliance with industry standards such as OSHA, API, ASME, and ISO. --Lead and mentor a multidisciplinary team focused on maintenance and reliability best practices. --Facilitate Process Hazard Analyses...
- ...process engineering projects, continuous improvement initiatives, and manufacturing operations while maintaining compliance with GMP and ISO standards. Responsibilities Support engineering projects and programs of low to medium complexity Assist with process...Full timeWork at officeVisa sponsorship
- ...extra hours ~ Preferable: Prior experience with supplier quality programs in medical device industry ~ Preferable: Familiarity with ISO 13485 and supplier quality metrics At Validation & Engineering Group, people always come first. We believe that when you're...Full time
- ...cleanrooms. • Establish routine and non-routine cleaning schedules, procedures, and workflows for classified manufacturing areas (e.g., ISO 5–8). • Perform hands-on cleaning activities within cleanroom environments in accordance with cGMPs, SOPs, and aseptic practices....Local area
- ...role involves investigations, nonconformance management, process validation, and cross-functional collaboration to maintain FDA and ISO compliance while driving continuous improvement. Responsibilities Develop, modify, and maintain quality standards and protocols...
- ...process validation activities and collaborate with cross-functional teams Analyze manufacturing data and ensure compliance with GMP, ISO, and safety standards Requirements Completion of undergraduate freshman year at accredited university Pursuing Bachelor's...Full timeVisa sponsorship
