R&D Project Manager
Aptyx - Charlotte, North Carolina, United States, 28245
Work at Aptyx
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R&D Manager
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Southwest Mold, Inc dba Seitz, Aptyx
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R&D Manager
role at
Southwest Mold, Inc dba Seitz, Aptyx
Job Description: R&D Engineering Manager Position:
R&D Engineering Manager
Location:
Charlotte, NC
Department:
Development
Reports to:
Director of Development
Company Overview At Aptyx, a new name backed by 70 years of expertise, we bring together the aptitude and excellence of more than a dozen companies with decades of experience helping customers in the life sciences and other demanding industries solve complex manufacturing problems with confidence so they can create more good things in the world. We are committed to delivering high-quality products and services to our customers worldwide. We are seeking a talented and experienced R&D Engineering Manager to join our dynamic team and contribute to our mission of excellence and innovation.
Job Summary The R&D Engineering Manager performs as a design engineer and group manager for product development work on medical devices in the Development department. The primary goal is to lead and coordinate project engineers, technicians, and assemblers to conduct development projects on time and within budget, meeting customer objectives and project success criteria. The manager will coordinate activities, provide guidance, and may serve as project manager in some cases.
Key Responsibilities
Customer Satisfaction:
Support product development teams to ensure customer satisfaction, communicate with customers, resolve issues, and report project status.
Resource Management:
Assign team members to projects, balance workloads, and coordinate with other departments for resource availability.
Training and Development:
Mentor staff, oversee collaboration with vendors, and manage hands-on development of catheter, implant, and other disposable products.
Financial Management:
Support department financial goals, manage costs, revenues, and review invoices.
Technical Support:
Provide technical troubleshooting, supervise documentation for quality systems.
Quality Assurance:
Ensure design practices comply with QMS and regulatory requirements.
Sales Support:
Participate in project quotations, budgets, and timelines.
Data Analysis:
Use analytics to support KPIs, prepare reports for management.
Continuous Improvement:
Recommend and support process and practice improvements.
Additional Responsibilities:
Other duties to support the department and company.
Qualifications
BS or MS in Engineering (Biomedical or Mechanical preferred).
Minimum 8 years in medical device development, 10+ preferred; supervisory experience is a plus.
Experience with regulatory requirements, quality systems, and medical device applications.
Technical skills in device design, materials, prototyping, and project management.
Excellent problem-solving, communication, and interpersonal skills.
Willingness to travel domestically and internationally.
Benefits
Competitive salary and bonuses
Health, dental, vision insurance
Retirement plan with company match
Paid time off and holidays
Professional development opportunities
Relocation assistance if applicable
Additional Details
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Research, Analyst, and IT
Industry: Plastics Manufacturing
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