Sr Manufacturing Engineer
Job in
Lafayette, Boulder County, Colorado, 80026, USA
Listed on 2026-06-26
Listing for:
Planet Pharma
Full Time
position Listed on 2026-06-26
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering, Process Engineer, Validation Engineer -
Manufacturing / Production
Manufacturing Engineer, Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Pay 55-65/h depending on experience
Top 3 technical skills that you are required for the role- Technical Project Management
- Manufacturing Equipment Development
- Process Engineering
Bachelor’s degree in a technical field
Years of Experience RequiredMinimum 4 years
Job DetailsContractor will work 40 hours per week, onsite 5 days a week. Interviews scheduled 1 week after posting. Product line:
Electrosurgical Hardware.
This position is for an Advanced Manufacturing Engineer (Technical Equipment Lead). This role will support a Project Manager during implementation of a production line for a new medical device (electronic hardware).
Responsibilities- Management of Manufacturing Equipment Development Strategy
- Leading and organizing a project team for manufacturing equipment development.
- Creating and allocating tasks to team members. Monitor progress on all deliverables.
- Maintain schedule for manufacturing deliverables and working with Project Manager to integrate deliverables into overarching program schedule.
- Work with cross-functional team to create requirements flow down to connect product specifications to manufacturing test processes.
- Support qualification of new production line:
- Development and validation for new production processes.
- Manage product BOM configurations in PLM system.
- Integrate new components with manufacturing ERP/MRP systems.
- Develop and execute plans, including statistical analysis, to evaluate process repeatability through equipment qualification and process validation (IQ/OQ/PQ).
- Perform Test Method Validation and Software Validation for hardware test systems.
- Define and generate all required documentation in support of manufacturing protocols, reports, changes, and manufacturing instructions. These include Engineering protocols, reports, process risk documents (PFMEA), manufacturing instructions, change orders and statistical analysis.
- Generate documents and BOM structures to support service depots.
- Provide engineering support to manufacturing operations and address quality issues arising on the production floor.
- Bachelor’s Degree in a technical discipline
- Minimum 4 years of experience required.
- Master’s Degree in a technical discipline
- Medical Device and/or Manufacturing Experience
- Experience in an electronics manufacturing environment
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