Job Role : MCAD Administrator - Medical Device (Arden Hills, MN) Contract Mid-level (Hybrid)
Overview :
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues.
We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology.
Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at and follow us on LinkedIn :
Our Fortune 500 Medical Device client has a n exciting opportunity for MCAD Administrator.
Job Summary :
We have an exciting opportunity for an MCAD Administrator with a strong background in SolidWorks and SolidWorks PDM Professional software(s) and associated data management processes.
This role will be responsible for managing migration of acquired MCAD data and harmonizing engineering applications into client systems.
Technical expertise and creative problem-solving skills will play a crucial role in successfully onboarding acquisitions.
Responsibilities :
- Assess acquired MCAD Data for quality level and provide resource / remediation estimates.
- Attend and contribute to Kaizen Sessions for holistic Migration / Integration process and schedule.
- Develop and Document MCAD Migration Strategies with Cross Functional Groups (R&D, Quality, Supplier Engineering, Process Engineering, etc.
including Acquired Stakeholders.
- Train Acquired Design teams on newly developed processes for MCAD and data management.
- Host cross functional meetings (weekly) with Integration CAD resources.
- Collaborate with IT during Laptop Rollout for acquired resources.
- Resolve issues / strategy / timeline changes as they arise.
- Identify Lessons Learned in Migration / Integration process allowing for efficiency gains in future acquisitions.
- Provide technical support and troubleshooting for CAD-related issues.
- Develop and maintain CAD standards, procedures, and best practices.
- Train and support users on CAD software and tools, ensuring proper usage.
- Collaborate with design teams to optimize CAD workflows and processes.
- Assist in the development and implementation of CAD training programs.
- Coordinate with IT to ensure CAD systems are integrated with other technologies.
- Maintain documentation for CAD standards, libraries, and user guides.
- Domestic and International travel is required (0-30%).
Minimum requirements :
Bachelor’s degree in mechanical engineering , Aerospace, or a related field, including :
5-7 years’ experience in 3D MCAD (e.g., SolidWorks, Creo, Catia, Inventor, SolidEdge , OnShape experience.)
- Proven experience as a MCAD Administrator or in a similar role.
- Strong technical proficiency in MCAD Data management, with a deep understanding of quality MCAD Data practices.
- Advanced problem-solving skills and the ability to develop solutions for complex MCAD data remediation challenges.
- Excellent communication and collaboration skills with the ability to adapt to the target audience.
- Demonstrated ability to thrive in a fast-paced, agile environment.
Preferred Qualifications
- Certified SolidWorks Professional (CSWP) or Certified SolidWorks Expert (CSWE)
- Mechanical CAD PDM System Experience (SolidWorks PDM or similar systems)
Other Details :
Schedule : Either 7-4 : 30pm CT, or 8-5pm - some flex.
Contract Length : 7 months
Hybrid (onsite 3 days)
Travel : 30% over a year duration, including domestic & International travel.
Possible temp to hire for right individual.
EEO Employer :
Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law.
Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law.
If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact .
Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients.
When you join Pharmavise, you become part of a team that values Excellence Through Quality.
E-Verify Participation :
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