Reliability Engineer improves reliability, maintainability, safety, and lifecycle performance of manufacturing, utility, facility, and process systems.
Compensation
The salary range for this position is: $100,500.00 - $145,166.66
Responsibilities
Analyze CMMS/EAM data, downtime, deviations, work orders, maintenance costs, condition-monitoring results, spare-parts usage, and equipment history.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Salary Range 107,545.40USD -145,502.60 USD
Responsibilities
Own, manage, and close quality records (Supplier Event Notifications and Investigations (EN/SICAR), Change Controls, Deviations, Corrective and Preventive Actions (CAPAs), and CAPA-Effectiveness Verifications) under the company's quality management system procedures and ensure compliance with regulatory agency requirements.
Facilitation of cross-functional teams (internal and external to the site) with the goal of achieving robust and detailed investigation performance or timely implementation of supplier/raw material related changes.
Partner cross-functionally across the network to ensure maturity and execution of robust quality record process.
Lead investigation teams to identify meaningful root causes and robust corrective and preventative actions by effectively utilizing advanced root cause analysis tools (Causal Factor Analysis, Fault Tree Analysis, Kepner-Tregoe, etc.).
Manages closure of multiple quality records simultaneously and in a timely matter (Deviations, Change Controls, ENs, SICARs, CAPA, CAPA-EV).
Supervisor, Quality Control (Chemistry) overseeing method transfer and quality processes at Cardinal Health.
Compensation
Anticipated salary range: $82,100.00-$117,200.00
Responsibilities
Coordinates and supervises the daily activities of Chemists or business support staff in the performance of technology transfer, method validation/verification and method optimization
Serves as the liaison between Cardinal Health Quality Control and Client Quality Control in the performance of technology transfer, method validation/verification/development/optimization
Is a quality lead for the QC Chemistry team
Identifies quality events and works with QA/QC management to ensure each event is handled in accordance with site procedures and regulatory requirements
Oversees chemists and contractors who operate analytical equipment, perform analytical tests, interpret results and documents findings in accordance with SOPs and regulatory requirements
Requirements
Bachelor’s degree in chemistry or related science field
The role manages capital projects and serves as system owner for assigned clean utility systems and equipment, sustaining facilities and equipment through troubleshooting and service-ordination.
Compensation
The base compensation range for this role is $95,000-$125,000.
Responsibilities
Manage capital projects for facility, laboratory, utility, infrastructure, and process-support equipment from initial assessment through closeout.
Develop project scopes, option assessments, cost estimates, capital requests, budgets, schedules, risk assessments, and execution plans for new equipment and facility improvements.
Coordinate user requirements, engineering specifications, design reviews, RFPs, bid evaluations, procurement recommendations, and project documentation.
Manage A/E firms, construction contractors, OEMs, service providers, RFIs, submittals, change orders, field coordination, startup, FAT/SAT, commissioning, and turnover activities.
Monitor project scope, cost, commitments, forecast, schedule, risks, and changes; communicate status, decisions, constraints and mitigation plans to stakeholders and leadership.
Requirements
Bachelor’s of Science degree in engineering or related technical discipline
Quality Assurance Specialist (m/f/d) in Berlin, responsible for maintaining and improving the Quality Management System, managing quality events, supporting audits, and driving continuous improvement initiatives.
Responsibilities
Help maintain and continuously improve our Quality Management System (QMS) in line with ISO 9001 and internal quality requirements.
Take ownership of quality events including deviations, non-conformances, CAPAs and change controls, assessing actions, tracking effectiveness and helping ensure timely closure.
Keep our documentation robust and inspection-ready through effective document control and eQMS administration.
Support internal and external audits, from preparation and documentation through to follow-up actions.
Help ensure training requirements and quality records remain accurate, compliant and up to date.
Requirements
A degree in Science, Quality, Engineering, Biotechnology, Chemistry, Life Sciences or a related field.
Responsible for ensuring uninterrupted manufacturing operations, and escalating issues when appropriate.
Support manufacturing activities associated with system integration and test.
Work directly with Manufacturing Associates and cross-functional engineering partners to identify and resolve technical issues affecting safety, quality, delivery, or production continuity.
Investigate manufacturing test failures using structured troubleshooting and problem-solving methods.
Troubleshoot test hardware, software, and system interfaces.
The Experienced Operations Process Engineer supports manufacturing execution for the OTTAVA Capital System production line, providing technical support, process ownership, and continuous improvement on the shop floor.
Compensation
The anticipated base pay range for this Bay Area position is:
$94,000.00 - $150,650.00
Responsibilities
Serve as the process owner for assigned system integration, assembly, and test processes
Provide timely technical support for manufacturing interruptions
Ensure manufacturing work instructions, specifications, process records, and traceability controls are accurate
Define tooling, fixture, equipment, and metrology requirements
Lead structured investigations of complex mechanical, electromechanical, software, and system-level manufacturing and test failures
Requirements
Bachelor's degree in Mechanical, Manufacturing, Industrial, Systems, Biomedical, Mechatronics, Electrical, or a related engineering discipline
Nice to have: Experience manufacturing surgical robotics
Nice to have: Medical capital equipment
Nice to have: Robotic systems
Nice to have: Safety-critical electromechanical products
Responsible for manufacturing and device quality for commercial devices and manufacturing transfers, owning sustaining activities for investigational and commercial device manufacturing.
Compensation
Salary range: $130,000 to $170,000 based on skills and experience
Responsibilities
Process risk assessment (PFMEA)
Master Validation Plan(s) and Report(s)
Failure/Scrap code identification and maintenance
Manufacturing, process monitoring, and product acceptance plans
Draft, collaborate, and approve project deliverables and engineering work orders
Engineer (Facilities & Engineering and Capital Projects)NewCelgard · Fremont, US