Veranex
Veranex’s mission as an Innovation CRO is to improve patient outcomes by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on MedTech, we take clients’ Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role Manufacturing Engineer 1 or 2
performs and coordinates broad manufacturing engineering activities in the development and supply of capital and disposable medical devices and instruments.
What You Will Do
Perform manufacturing engineering functional lead duties including engineering and production builds, assembly line/cell layout, process flow development, process development, manufacturing fixture design, operator manufacturing/assembly training, etc.
Provide technical project management through continuous communication with internal design, engineering, quality, and manufacturing personnel, OEM factories, suppliers, and clients regarding manufacturing engineering progress and details of multiple projects.
Work with Quality Engineering to execute GMP and testing procedures to ensure compliance with design output specifications and lifecycle requirements.
Maintain manufacturing files and databases per internal design control procedures.
Define and generate all required documentation in support of manufacturing products and processes.
Design and determine manufacturing text fixtures with minimal guidance from senior staff.
Provide support to improve, maintain, or fix manufacturing processes.
Execute training operators for manufacturing/assembly with minimal guidance from senior staff.
Troubleshoot project related manufacturing issues with minimal guidance from senior staff.
Support the organization in meeting production schedules through resolving technical, equipment, or operational issues.
Support initiatives to improve safety and compliance to applicable regulations. Participate in build and release plans.
Qualifications Manufacturing Engineer 1
Bachelor’s degree in manufacturing or mechanical engineering and 1–3 years of relevant work experience.
Good knowledge of overall medical device industry.
Good knowledge of computer-aided design (CAD) packages.
Good knowledge of process development.
Good written and oral communication skills.
Attention to detail.
Ability to multi‑task and perform a wide range of activities.
Ability to work under a timeline.
Ability to solve basic to moderate technical problems.
Manufacturing Engineer 2
Bachelor’s degree in manufacturing or mechanical engineering and 2–4 years of relevant work experience, or Master’s degree and 1–3 years of relevant work experience.
Experience working with minimal guidance on day‑to‑day work.
Strong knowledge of overall medical device industry.
Strong knowledge of computer-aided design (CAD) packages.
Strong knowledge of process development and process validation.
Strong written and oral communication skills.
Excellent attention to detail.
Ability to multi‑task and perform a wide range of activities.
Ability to work under a timeline.
Ability to solve moderate to complex technical problems.
Preferred
Experience with medical device manufacturing industry.
UDI labeling experience.
Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.
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About This Role Manufacturing Engineer 1 or 2
performs and coordinates broad manufacturing engineering activities in the development and supply of capital and disposable medical devices and instruments.
What You Will Do
Perform manufacturing engineering functional lead duties including engineering and production builds, assembly line/cell layout, process flow development, process development, manufacturing fixture design, operator manufacturing/assembly training, etc.
Provide technical project management through continuous communication with internal design, engineering, quality, and manufacturing personnel, OEM factories, suppliers, and clients regarding manufacturing engineering progress and details of multiple projects.
Work with Quality Engineering to execute GMP and testing procedures to ensure compliance with design output specifications and lifecycle requirements.
Maintain manufacturing files and databases per internal design control procedures.
Define and generate all required documentation in support of manufacturing products and processes.
Design and determine manufacturing text fixtures with minimal guidance from senior staff.
Provide support to improve, maintain, or fix manufacturing processes.
Execute training operators for manufacturing/assembly with minimal guidance from senior staff.
Troubleshoot project related manufacturing issues with minimal guidance from senior staff.
Support the organization in meeting production schedules through resolving technical, equipment, or operational issues.
Support initiatives to improve safety and compliance to applicable regulations. Participate in build and release plans.
Qualifications Manufacturing Engineer 1
Bachelor’s degree in manufacturing or mechanical engineering and 1–3 years of relevant work experience.
Good knowledge of overall medical device industry.
Good knowledge of computer-aided design (CAD) packages.
Good knowledge of process development.
Good written and oral communication skills.
Attention to detail.
Ability to multi‑task and perform a wide range of activities.
Ability to work under a timeline.
Ability to solve basic to moderate technical problems.
Manufacturing Engineer 2
Bachelor’s degree in manufacturing or mechanical engineering and 2–4 years of relevant work experience, or Master’s degree and 1–3 years of relevant work experience.
Experience working with minimal guidance on day‑to‑day work.
Strong knowledge of overall medical device industry.
Strong knowledge of computer-aided design (CAD) packages.
Strong knowledge of process development and process validation.
Strong written and oral communication skills.
Excellent attention to detail.
Ability to multi‑task and perform a wide range of activities.
Ability to work under a timeline.
Ability to solve moderate to complex technical problems.
Preferred
Experience with medical device manufacturing industry.
UDI labeling experience.
Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.
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