Job details Product Support Engineer role - On Site.
This 6-month contract position (with potential for extension) is essential to the expansion of our client's worldwide technical service centers. We are seeking a skilled and motivated engineer to industrialize the critical equipment used for product servicing, ensuring consistent quality and efficiency in global service operations within a regulated industry. ...
Responsibilities:
Job Description (Essential Functions)
Job Description (Essential Functions)
Lead the full lifecycle (development, prototyping, industrialization, documentation, and release) of custom tools and fixtures required to service advanced complex electronic and mechanical medical devices.
Partner with the dedicated Service Team to identify equipment needs, implement design improvements, and optimize service equipment workflows for efficient repair operations.
Develop all required engineering documentation for tool release, including comprehensive assembly instructions, mechanical drawings, Bills of Materials (BOMs), and formal validation reports.
Drive the formal release of service tools into the Document Control System, managing their industrialization to ensure readiness for successful global deployment across multiple technical centers.
Support the rigorous qualification, verification, and validation (IQ/OQ/PQ) of all service tools in strict accordance with medical device regulatory and quality system requirements (e.g., ISO 13485, FDA).

Working hours: 6:00 AM - 2:30 PM

Skills:
Preferred Skills & Knowledge
Familiarity with manufacturing process development, validation, and documentation in a tightly controlled quality system environment.
Experience in process improvement and cost reduction initiatives, contributing to overall global service readiness and efficiency.
Basic knowledge of Lean Manufacturing concepts such as Design for Manufacturing (DFM), Design of Experiments (DOE), and product/process Failure Mode and Effects Analysis (FMEA).
Excellent communication and cross-functional collaboration skills to effectively work with R&D, Production Engineering, Procurement, and external suppliers.
Experience collaborating with internal manufacturing resources and external vendors to ensure timely delivery and high-quality fabrication of specialized service equipment.

Education:
Bachelors

Experience:
1-4 years

Qualifications:
Required Skills & Experience
Bachelor?s degree in Mechanical Engineering or a closely related technical discipline.
3+ years of relevant experience in manufacturing engineering, product support, or tooling design?specifically within the medical device or other highly regulated industry.
Demonstrated expertise with CAD software (SolidWorks preferred) and foundational knowledge of mechanical design principles and Geometric Dimensioning and Tolerancing (GD&T).
Direct experience with electronics assembly, including computer interfaces, PC boards, enclosures, test software and mechanical devices.
Proven ability to manage multiple simultaneous projects under tight delivery timelines while maintaining robust documentation and quality standards.


If your validation and tooling design experience meets these specialized medical device requirements, click apply and submit your resume now for immediate consideration!

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.

Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Show lessShow more Product Support Engineer role - On Site.
This 6-month contract position (with potential for extension) is essential to the expansion of our client's worldwide technical service centers. We are seeking a skilled and motivated engineer to industrialize the critical equipment used for product servicing, ensuring consistent quality and efficiency in global service operations within a regulated industry.

Responsibilities:
Job Description (Essential Functions)
Job Description (Essential Functions)
Lead the full lifecycle (development, prototyping, industrialization, documentation, and release) of custom tools and fixtures required to service advanced complex electronic and mechanical medical devices.
Partner with the dedicated Service Team to identify equipment needs, implement design improvements, and optimize service equipment workflows for efficient repair operations.
Develop all required engineering documentation for tool release, including comprehensive assembly instructions, mechanical drawings, Bills of Materials (BOMs), and formal validation reports.
Drive the formal release of service tools into the Document Control System, managing their industrialization to ensure readiness for successful global deployment across multiple technical centers. ... Support the rigorous qualification, verification, and validation (IQ/OQ/PQ) of all service tools in strict accordance with medical device regulatory and quality system requirements (e.g., ISO 13485, FDA).

Working hours: 6:00 AM - 2:30 PM

Skills:
Preferred Skills & Knowledge
Familiarity with manufacturing process development, validation, and documentation in a tightly controlled quality system environment.
Experience in process improvement and cost reduction initiatives, contributing to overall global service readiness and efficiency.
Basic knowledge of Lean Manufacturing concepts such as Design for Manufacturing (DFM), Design of Experiments (DOE), and product/process Failure Mode and Effects Analysis (FMEA).
Excellent communication and cross-functional collaboration skills to effectively work with R&D, Production Engineering, Procurement, and external suppliers.
Experience collaborating with internal manufacturing resources and external vendors to ensure timely delivery and high-quality fabrication of specialized service equipment.

Education:
Bachelors

Experience:
1-4 years

Qualifications:
Required Skills & Experience
Bachelor?s degree in Mechanical Engineering or a closely related technical discipline.
3+ years of relevant experience in manufacturing engineering, product support, or tooling design?specifically within the medical device or other highly regulated industry.
Demonstrated expertise with CAD software (SolidWorks preferred) and foundational knowledge of mechanical design principles and Geometric Dimensioning and Tolerancing (GD&T).
Direct experience with electronics assembly, including computer interfaces, PC boards, enclosures, test software and mechanical devices.
Proven ability to manage multiple simultaneous projects under tight delivery timelines while maintaining robust documentation and quality standards.


If your validation and tooling design experience meets these specialized medical device requirements, click apply and submit your resume now for immediate consideration!

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.

Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Show lessShow morekey responsibilities

Job Description (Essential Functions)Job Description (Essential Functions)Lead the full lifecycle (development, prototyping, industrialization, documentation, and release) of custom tools and fixtures required to service advanced complex electronic and mechanical medical devices.Partner with the dedicated Service Team to identify equipment needs, implement design improvements, and optimize service equipment workflows for efficient repair operations.Develop all required engineering documentation for tool release, including comprehensive assembly instructions, mechanical drawings, Bills of Materials (BOMs), and formal validation reports.Drive the formal release of service tools into the Document Control System, managing their industrialization to ensure readiness for successful global deployment across multiple technical centers.Support the rigorous qualification, verification, and validation (IQ/OQ/PQ) of all service tools in strict accordance with medical device regulatory and quality system requirements (e.g., ISO 13485, FDA).

experience

1-4 years

skills

Preferred Skills & KnowledgeFamiliarity with manufacturing process development, validation, and documentation in a tightly controlled quality system environment.Experience in process improvement and cost reduction initiatives, contributing to overall global service readiness and efficiency.Basic knowledge of Lean Manufacturing concepts such as Design for Manufacturing (DFM), Design of Experiments (DOE), and product/process Failure Mode and Effects Analysis (FMEA).Excellent communication and cross-functional collaboration skills to effectively work with R&D, Production Engineering, Procurement, and external suppliers.Experience collaborating with internal manufacturing resources and external vendors to ensure timely delivery and high-quality fabrication of specialized service equipment.

qualifications

Required Skills & ExperienceBachelor?s degree in Mechanical Engineering or a closely related technical discipline.3+ years of relevant experience in manufacturing engineering, product support, or tooling design?specifically within the medical device or other highly regulated industry.Demonstrated expertise with CAD software (SolidWorks preferred) and foundational knowledge of mechanical design principles and Geometric Dimensioning and Tolerancing (GD&T).Direct experience with electronics assembly, including computer interfaces, PC boards, enclosures, test software and mechanical devices.Proven ability to manage multiple simultaneous projects under tight delivery timelines while maintaining robust documentation and quality standards.

education

Bachelors

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