Goddard is seeking a Manufacturing Engineer to join our team. This position is responsible for designing, implementing, and reviewing the procedures and equipment involved in the manufacturing process. Their duties include researching automation techniques, testing new systems for efficiency and planning factory layouts to optimize production. In addition, they will be responsible for providing manufacturing engineering support in new product introduction, and development of anything necessary to complete design transfer through commercialization of medical device products. The ideal candidate must have a strong track record in medical device or other quality systems within a manufacturing environment. Excellent interpersonal and communication skills, as well as the ability to manage across functions, and multidisciplinary projects are key attributes to be successful in this role.

About the Role:

• Evaluate quality control processes and make recommendations for improvements in quality control.
• Analyze production processes, schedules, methods, and other data and then provide management with reports containing the data and statistics to enable management to better understand future requirements needed for the manufacturing process.
• Ensure that the Company’s manufacturing processes follow all government laws and regulations.
• Review and calculate labor, material, and other production costs along with reviewing schedules and future production requirements to assist management in decision making.
• Analyze and plan workflow, equipment placement and space requirements to improve manufacturing efficiency.
• Coordinate equipment maintenance and repair services and make sure that manufacturer’s procedures and instructions are followed to keep production equipment operational.
• Facilitate the application of design controls through all phases of the product development process.
• Review design development, and design change documents to ensure that all documentation include the necessary justifications, validation and verification updates, risk assessments, etc.
• Provide quality engineering support for product development teams.
• Author, and review documents for content, accuracy, and completeness.

About You:

• Bachelor’s degree in science or engineering is preferred.
• 5 years minimum hands-on working knowledge of the FDA QSR and ISO 13485 is required. 
• Experience with test methods and standards for the design, verification, and validation of medical device products.
• Highly skilled in statistical methods, gage R&R, statistical process control, sampling plans, and design of experiments.
• Highly proficient using the Microsoft Office Suite including Excel, Word, and PowerPoint. Minitab or other statistical software a plus.
• Self-motivated, possess strong organizational skills, and outstanding written and verbal communication skills.
• A positive, team-player attitude.
• Ability to multi-task, meet tight deadlines, and prioritize changing demands in a fast-paced, entrepreneurial environment.
• Proven accuracy, thoroughness, and attention to detail in reviewing and completing quality records.

COVID-19 Consideration: We require all our employees to be fully vaccinated in order to safeguard the health and wellbeing of our employees, families, customers, and visitors. Please note: Presently, Goddard does not sponsor employment visas.

Please note: Presently, Goddard does not sponsor employment visas.

Goddard believes that everyone is entitled to fair opportunities and equal employment rights. We comply with all applicable laws prohibiting discrimination in hiring and the terms and conditions of employment including, but not limited to, compensation, promotion, discipline, or termination. Goddard is firm on its policy to provide equal employment opportunity for all employees and applicants on the basis of qualification and merit and will not discriminate on the basis of race, color, creed, religion, national origin, age, disability, genetic information, sex, sexual orientation, gender identity, marital status, veteran status, public assistance status, membership or activity in a local commission, or any other legally protected status in accordance with applicable local, state, and federal laws.