HybridDescription:Job Summary:Lead cross-functional teams in complex engineering assignments, ensuring compliance with medical device regulations and effective project execution. This role requires a strong focus on project management, collaboration, and problem-solving across traditional product lines.Primary ResponsibilitiesIndependently plan, execute, and direct cross-functional engineering projects, adapting standard engineering principles to develop innovative solutions.Manage projects consisting of cross-functional teams (including but not limited to regulatory, risk management, quality, technical communications, and supplier quality)Oversee all financial aspects of product development, including capital expenditures and cross-functional expenses.Identify and resolve complex problems, developing new solutions as needed for project roadblocksKnowledgeMedical Device Regulations: In-depth understanding of FDA regulations, ISO standards, and other relevant guidelines governing medical device labeling and compliance.Project Management Methodologies: Familiarity with project management frameworks (e.g., Agile, Waterfall) and tools (e.g., Gantt charts, project management software).Engineering Principles: Strong foundation in engineering principles relevant to medical device design and development.Quality Management Systems (QMS): Knowledge of QMS practices and documentation requirements.Cross-Functional Team Dynamics: Understanding of the roles and responsibilities of various departments involved in medical device development.SkillsProject Management Skills: Proven ability to manage multiple projects simultaneously, ensuring timely delivery within budget.Analytical Skills: Strong analytical and problem-solving skills to identify issues and develop effective solutions.Communication Skills: Excellent verbal and written communication skills for diverse audiences.Leadership Skills: Ability to lead and motivate cross-functional teams.Attention to Detail: Meticulous attention to detail in reviewing labeling documentation.AbilitiesIndependent Judgment: Ability to make informed decisions in evaluating engineering techniques.Adaptability: Flexibility to adapt to changing project requirements and industry trends.Time Management: Strong organizational skills with effective prioritization.Interpersonal Skills: Ability to build and maintain positive working relationships.Continuous Learning: Commitment to staying current with industry developments.QualificationsBachelor’s degree in Engineering or a related field.8-10 years of relevant experience in project management, with a focus on medical devices.2-5 years of experience in matrix management.Thorough, up-to-date knowledge of multiple engineering disciplines.Notes:Hybrid9:00am-5:00pmVIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status
Description:Job Summary:Lead cross-functional teams in complex engineering assignments, ensuring compliance with medical device regulations and effective project execution. This role requires a strong focus on project management, collaboration, and problem-solving across traditional product lines.Primary ResponsibilitiesIndependently plan, execute, and direct cross-functional engineering projects, adapting standard engineering principles to develop innovative solutions.Manage projects consisting of cross-functional teams (including but not limited to regulatory, risk management, quality, technical communications, and supplier quality)Oversee all financial aspects of product development, including capital expenditures and cross-functional expenses.Identify and resolve complex problems, developing new solutions as needed for project roadblocksKnowledgeMedical Device Regulations: In-depth understanding of FDA regulations, ISO standards, and other relevant guidelines governing medical device labeling and compliance.Project Management Methodologies: Familiarity with project management frameworks (e.g., Agile, Waterfall) and tools (e.g., Gantt charts, project management software).Engineering Principles: Strong foundation in engineering principles relevant to medical device design and development.Quality Management Systems (QMS): Knowledge of QMS practices and documentation requirements.Cross-Functional Team Dynamics: Understanding of the roles and responsibilities of various departments involved in medical device development.SkillsProject Management Skills: Proven ability to manage multiple projects simultaneously, ensuring timely delivery within budget.Analytical Skills: Strong analytical and problem-solving skills to identify issues and develop effective solutions.Communication Skills: Excellent verbal and written communication skills for diverse audiences.Leadership Skills: Ability to lead and motivate cross-functional teams.Attention to Detail: Meticulous attention to detail in reviewing labeling documentation.AbilitiesIndependent Judgment: Ability to make informed decisions in evaluating engineering techniques.Adaptability: Flexibility to adapt to changing project requirements and industry trends.Time Management: Strong organizational skills with effective prioritization.Interpersonal Skills: Ability to build and maintain positive working relationships.Continuous Learning: Commitment to staying current with industry developments.QualificationsBachelor’s degree in Engineering or a related field.8-10 years of relevant experience in project management, with a focus on medical devices.2-5 years of experience in matrix management.Thorough, up-to-date knowledge of multiple engineering disciplines.Notes:Hybrid9:00am-5:00pm
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