Energy Jobline ZR
Engineering Project Manager - Non IT in Skaneateles Falls
Energy Jobline ZR, Skaneateles Falls, New York, us, 13153
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.
Responsibilities
Independently 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 roadblocks.
Identify key project members and milestones required to the project (Project Scoping).
Work cross‑functionally with internal and external parties (R&D, Technical Communications, Suppliers, etc.).
Provide updates on project status on a weekly basis.
Execute projects to closure in a timely manner.
Ensure that output meets the project intent once closed.
Document all project key decisions and evidence of milestone completions, that the project documentation is auditable and compliant to all Medical Device Industry requirements.
Knowledge
Medical 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.
Skills
Project 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.
Abilities
Independent 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.
Qualifications
Bachelor’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.
PMP certification is preferred.
Regulated industry experience.
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
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Responsibilities
Independently 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 roadblocks.
Identify key project members and milestones required to the project (Project Scoping).
Work cross‑functionally with internal and external parties (R&D, Technical Communications, Suppliers, etc.).
Provide updates on project status on a weekly basis.
Execute projects to closure in a timely manner.
Ensure that output meets the project intent once closed.
Document all project key decisions and evidence of milestone completions, that the project documentation is auditable and compliant to all Medical Device Industry requirements.
Knowledge
Medical 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.
Skills
Project 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.
Abilities
Independent 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.
Qualifications
Bachelor’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.
PMP certification is preferred.
Regulated industry experience.
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
#J-18808-Ljbffr