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Job Title: Senior Systems Engineer, Medical Device Technical Lead (JP11791)
Location: Thousand Oaks, CA.
Business Unit: Final Product Technical Leads
Employment Type: Contract
Duration: 18 Months with possible extensions or conversion to FTE
Rate: $46 - $51/hour W2
Posting Date: 09/19/2023
Notes: Qualified candidates with either a strong Electrical Engineering, Mechanical Engineering, OR Systems/Software Engineering background need apply and will be considered. Candidates must elaborate on their experience in Excel macros and product development on their resume.
3 Key Consulting is recruiting a Senior Systems Engineer, Medical Device Technical Lead for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
Top Must Have Skill Sets:
Day to Day Responsibilities:
Basic Qualifications:
Preferred Qualifications:
Why is the Position Open?
Planned Project.
Red Flags:
Interview Process:
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA.
Business Unit: Final Product Technical Leads
Employment Type: Contract
Duration: 18 Months with possible extensions or conversion to FTE
Rate: $46 - $51/hour W2
Posting Date: 09/19/2023
Notes: Qualified candidates with either a strong Electrical Engineering, Mechanical Engineering, OR Systems/Software Engineering background need apply and will be considered. Candidates must elaborate on their experience in Excel macros and product development on their resume.
3 Key Consulting is recruiting a Senior Systems Engineer, Medical Device Technical Lead for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
- Candidates must have experience in the biotechnology, pharmaceutical, or medical device industry.
- Candidates must have at least 5 years’ experience in systems engineering.
- Candidates must have great communication skills and can lead meetings and work teams.
- Candidates must have strong background in documenting requirements and providing traceability documentation for FDA approval
- DOORS
- Requisite Pro, or other similar requirements management software.
- Practical experience in configuration management and change control process/requirements, CCB (change control board), CIT (change implementation team) concepts experience is preferred.
- The Systems Engineer (SE) works as part of cross-functional program teams to deliver technical content, performance, intellectual property and quality deliverables of a combination product development program.
- The Systems Engineer understands and captures the user needs into system requirements and participates in the functional decomposition and allocation to subsystems.
- The Systems Engineer ensures that the quality targets are satisfied, identifies technical risks and assists risk retirement activities on the program.
- The Systems Engineer maintains close interaction with customers to understand and enhance the ability to deliver on customer satisfaction through high product quality.
Top Must Have Skill Sets:
- Systems Engineering past work experience.
- Ability to communicate effectively and lead large teams in development of technical deliverables required for design control deliverables.
- Past experience in writing SOPs, Guidance & technical documents is preferred but not required
- Proficient in Microsoft Excel especially in writing macros in excel.
Day to Day Responsibilities:
- Work cross-functionally with individuals and project teams in Marketing, Operations, and Development
- Create and assess product requirements to determine technical coverage and proper integration different subsystems.
- Create and execute to project plans and schedules
- Develop, execute, and review requirements documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects.
- Responsible for writing technical and guidance documents that provides guidance to team members in following design control and business processes within client.
- Develop Toolsets using Microsoft excel to enable easier on boarding of other engineers onto client processes
- Work and Lead cross functional teams in development of common practices and write technical guidance documents to enable consistency across various combination product teams.
Basic Qualifications:
- BS in Engineering and previous experience in a medical device industry.
- 10 years current experience with engineering processes and procedures.
Preferred Qualifications:
- 6+ years of progressive experience as an engineer or scientist within the appropriate field of study (Systems Engineering)
- Creative problem solver and solution developer when presented with conflicting requirements, business demands and technical risks/issues.
- Experience in combination product development.
Why is the Position Open?
Planned Project.
Red Flags:
- No degree
- No systems engineering experience
Interview Process:
- Video Conference with Hiring Manager.
- Selected candidates would then have a panel 1:1 video conference with additional team members.
- Candidate must be comfortable with video (webcam) online interview process.
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.