Description:
As a Manufacturing Engineer II, you will play a crucial role in the production of structural heart products. You will leverage your technical expertise, problem-solving abilities, and validation experience to ensure the efficiency and quality of our manufacturing processes. Your efforts will directly impact the improvement of our processes and the successful completion of our projects.
Key Responsibilities:
- Technical Expertise: Apply advanced engineering principles to support and improve manufacturing processes within the medical device sector.
- Problem Solving: Identify and resolve manufacturing issues to maintain product quality and production efficiency.
- Validation Experience: Conduct and document validation activities to ensure compliance with regulatory requirements and quality standards.
- Process Improvement: Continuously evaluate and enhance manufacturing processes to optimize productivity and reduce costs.
- Project Management: Lead and participate in project teams, ensuring timely completion of deliverables within budget.
- Teamwork: Collaborate effectively with cross-functional teams including R&D, Quality, and Operations to achieve common goals.
- Communication Skills: Clearly and effectively communicate technical information to team members, stakeholders, and management.
Qualifications:
- Minimum of 3 years of experience in a manufacturing engineering role, preferably within the medical device or related industry.
- Strong technical background with a proven track record in problem-solving and process improvement.
- Hands-on experience with validation processes and documentation.
- Excellent project management skills with the ability to manage multiple projects simultaneously.
- Effective teamwork and interpersonal skills.
- Strong verbal and written communication skills.