Argon Medical Devices is Hiring a Project Manager, CPS Near Plano, TX
Company Overview::
Argon Medical is a global manufacturer of specialty medical products, headquartered in Plano, Texas. Argon offers a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology and Oncology. Argon’s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. Our values describe what we believe in and how we operate. These values are our moral compass which guide our decisions and define the deeply held beliefs and principles of our organizational culture. Argon Medical is a family of individuals united by a mission and culture which continue to grow stronger every day.
Position Overview::
This position will manage projects related to the development, implementation and sustaining of CPS products and services for Argon Medical Devices. The selected candidate will interact with CPS customers, effectively manage and communicate project progress to management.
What you will do::
Responsible for the development and execution of semi-complex project/program plans.
Performs project/program management activities such as defining, scheduling, budgeting, risk management, change management, opportunity, and resource management.
Performs technical review of product/process design and documentation.
Assists with quoting new products/projects.
Performs active role in maintaining excellent customer relationship.
Provides engineering support for the development and manufacturing of new products. Evaluates proposed designs for manufacturability.
Creates drawings or models for new and existing products or fixtures.
Lead/supports process validation activities such as IQ/OQ/PQ.
Provides technical information concerning manufacturing or processing techniques, materials, properties, and process advantages and limitations to internal or external stakeholders for review or planning.
Compares product or equipment specifications with new product design and performance requirements to determine if new products can be produced by existing manufacturing methods.
Confers with planning and design staff concerning product design and tooling to ensure efficient production methods.
Confers with vendors to determine product specifications and arranges for purchase of equipment, materials or parts and evaluates products according to specifications and quality standards.
Develops, implements, trains and monitors effectiveness of engineering systems and procedures to ensure compliance to FDA, cGMP and all other applicable agency regulations.
Lead functional and cross-functional teams to achieve project goals.
Define problems, collect data, establish facts, and draw valid conclusions.
Skills for Success::
Bachelor’s degree or higher in Biomedical, Mechanical, Industrial, or other engineering.
Preferred: Master’s degree in biomedical, mechanical, industrial, or other engineering.
5 years related project management experience in an FDA/GMP regulated industry.
Familiar with AutoCAD, SolidWorks, Minitab, Word, excel and Project.
Working knowledge of manufacturing methods, procedures, and cost reduction/yield improvement techniques.
Experience with design, review, execution, and approval of installation, Operation and Process Qualification protocols and reports (IQ/OQ/PO).
Excellent verbal and written communication skills. Effective multi-channel communicator.
Proven record of delivering multi-disciplinary projects on time and on budget.
Ability to prioritize for maximum results (multi-task management)
Ability to perform successfully in a high paced,results oriented environment.