Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
New
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manager Medical Device Operations information
What is a manager medical device operations?
A Manager Medical Device Operations oversees the daily activities and processes involved in manufacturing, distributing, and maintaining medical devices. They ensure that operations comply with regulatory standards, manage teams, and work to optimize efficiency, quality, and safety. This role often involves coordinating with other departments, handling audits, and implementing process improvements to meet organizational goals. They play a critical role in ensuring that medical devices reach healthcare providers and patients safely and on time.
What are some common challenges faced by a manager medical device operations, and how can they be addressed?
Managers in Medical Device Operations often face challenges such as ensuring compliance with strict regulatory standards, coordinating cross-functional teams, and managing supply chain complexities. Staying proactive with regulatory updates, fostering open communication among departments, and implementing robust quality management systems can help address these issues. Additionally, investing in staff training and process improvement initiatives can streamline operations and minimize delays or compliance risks.
What are the key skills and qualifications needed to thrive as a manager medical device operations?
To excel as a Manager Medical Device Operations, you need expertise in supply chain management, regulatory compliance (such as FDA and ISO standards), and operational leadership, typically supported by a bachelor’s degree in engineering, life sciences, or business. Familiarity with ERP systems, quality management software, and relevant certifications like Six Sigma or PMP are commonly required. Strong communication, problem-solving, and team leadership skills help drive cross-functional collaboration and continuous improvement. These competencies are essential for ensuring product quality, regulatory adherence, and efficient operations in a highly regulated industry.
What are popular job titles related to Manager Medical Device Operations jobs in Ohio?
For Manager Medical Device Operations jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Manager Medical Device Operations jobs in Ohio look for?
The top searched job categories for Manager Medical Device Operations jobs in Ohio are:
- International Trade Coordinator
- Workplace Operations Manager
- Logistic Operations Manager
- Medical Device Logistics
- Quality Manager Medical Device
- Medical Device Territory Manager
- Clinical Operations Manager
- Logistics And Planning Manager
- Contract Senior Clinical Research Associate
- Logistics Operations Assistant
What cities in Ohio are hiring for Manager Medical Device Operations jobs?
Cities in Ohio with the most Manager Medical Device Operations job openings:
Full-time
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Job description
We are seeking a Medical Device Component Development Engineer to support component development, product lifecycle management, and engineering change activities for regulated medical devices. The ideal candidate will have expertise in design controls, verification & validation, supplier quality, process validation, and regulatory compliance.
Roles and Responsibilities- Lead component development and engineering change projects from concept to implementation.
- Manage project timelines, risks, and cross-functional coordination.
- Support Design Verification & Validation (V&V), test protocols, and technical documentation.
- Partner with suppliers on component qualification, DFM reviews, tooling, and process capability.
- Support manufacturing transfer, IQ/OQ/PQ, pilot builds, and production readiness.
- Apply Design Controls, PLM, ECO/ECN/ECR, Risk Management, and Quality System requirements.
- Review engineering drawings, GD&T, specifications, and acceptance criteria.
- Drive root cause analysis using CAPA, 8D, 5 Whys, and Fishbone methodologies.
- Communicate project status, risks, and technical recommendations to stakeholders.
- Experience in Medical Device Component Development or Product Development.
- Strong knowledge of:
- Product Lifecycle Management (PLM)
- Design Controls & Engineering Change Management (ECO/ECN/ECR)
- Design Verification & Validation (V&V)
- ISO 14971, DFMEA, PFMEA
- ISO 13485 & FDA 21 CFR Part 820/QMSR
- Supplier Quality Engineering & Design for Manufacturability (DFM)
- Process Validation (IQ/OQ/PQ)
- GD&T and engineering drawings
- Strong project management, communication, and problem-solving skills.
- Experience working with cross-functional teams in a regulated medical device environment.
- Medical Device Product Development
- Supplier Quality & Component Qualification
- Risk Management & Regulatory Compliance
- Manufacturing Transfer & Validation
- Root Cause Analysis (CAPA, 8D)
- Stakeholder & Project Management