Manufacturing Engineer III

This position will be responsible for coordinating product improvements according to customer specifications, addressing product manufacturing issues, and managing the product lifecycle. It requires utilizing a collaborative approach between customers, operations, production, supply chain, and research and development. It will also require working within a team environment, helping to improve manufacturing methods, systems, and processes to produce a high-quality product at an optimal cost.

DUTIES AND RESPONSIBILITIES:

• Coordination of product enhancements with customers and internal project teams
• Review high level design requirements to evaluate whether they are within Nextern core competency and vision; review design and determine required Bill of Materials
• Work with supply chain to obtain BOM pricing (from internal and external vendors)
• Responsible for Manufacturing issues as it relates to product quality and cost
• Support customer calls and presentations to compile product sustaining activities
• Help to generate all required documentation in support of the development and manufacturing products and processes, including timelines, responsibilities, engineering protocols, IQ, OQ, PQ reports, bill of materials, assembling instructions, manufacturing instructions and procedures.
• Help to conduct component and device testing protocols.
• Help to develop plans to evaluate process repeatability and stability through equipment qualification and process validation.
• Work with quality, supply chain and PD to ensure compliance with QSR and internal protocols.
• Works with internal manufacturing as well as outsourced partners to develop metrics such as labor time, yields, statistical analysis, qualification and validation of process, tooling and equipment.
• Transfer as required engineering project from engineering into manufacturing.

Requirements:
• Bachelor's degree in Electromechanical or Electrical Engineering or another

field related to Medical Devices and more than 5 or more years of related

experience and/or training, or an equivalent combination of education and

experience

• Advanced level of English

• Visa for USA and availability to travel for periods of 2-3 months

• Excellent oral and written communication skills

• Strong organizational, problem-solving, and analytical skills

• Ability to manage priorities and workflow

• Versatility, flexibility, and willingness to work within changing priorities with

enthusiasm

• Attention to detail

• Change control knowledge

• Proven ability to handle multiple projects and meet deadlines

• Good judgment with the ability to make sound and timely decisions

• Process Validation knowledge is required

• Proven work experience managing several production lines and multiple

resources of no less than 5 years, preferably in highly regulated industries such

as medical devices, pharmaceutical or the like.

• People-oriented and results-oriented.

• High sense of urgency and leadership, demonstrated ability to coach

operational and technical levels

• Exceptional interpersonal relationships across all levels

Benefits:
Competitive compensation package