Manufacturing Engineer
$35 - $40 per hourCollabera
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Days Left: 27 days, 3 hours left Apply To Discuss more about this job opportunity, please reach out to Anwesha Mohapatra (LinkedIn URL - Anwesha Mohapatra - Collabera | LinkedIn ) , email your updated resume at Email - View email address on click.appcast.io . Thank you! Pay Range: $35/hr to 40/hr Job Title: Manufacturing Engineer II Location: Minnetonka, MN 55343 Work Type: Onsite Contract Duration: 03 to 06 months with possible extension Job Summary:
- The Manufacturing Engineer II will provide technical leadership and engineering support within a regulated medical device manufacturing environment.
- The role will focus on manufacturing process development, process validation, risk assessment, process controls, and continuous improvement initiatives.
- The engineer will take ownership of complex technical assignments and develop effective solutions where established precedents may not exist.
- The position requires strong collaboration with internal teams, external stakeholders, suppliers, and engineering partners.
- The successful candidate will manage multiple projects while ensuring technical activities, timelines, and deliverables remain aligned with business objectives and quality requirements.
- Lead complex manufacturing engineering activities and provide technical direction for assigned projects.
- Support manufacturing processes through process validation, process controls, risk assessment, and continuous improvement activities.
- Develop and implement effective engineering solutions for manufacturing challenges while considering impacts across related systems and processes.
- Plan and manage project timelines, deliverables, technical activities, and cross functional dependencies.
- Collaborate with internal stakeholders, external partners, suppliers, quality teams, and engineering groups to resolve technical and operational issues.
- Support supplier changes and assess their impact on manufacturing processes, validation activities, and product quality.
- Participate in peer reviews and provide technical input for verification and validation activities.
- Identify potential manufacturing risks and recommend appropriate corrective and preventive actions.
- Bachelor of Science or Bachelor of Engineering degree in Mechanical Engineering, Electrical Engineering, Software Engineering, or a related engineering discipline.
- Minimum 5 to 6 years of Manufacturing Engineering experience within a Class III medical device environment.
- Strong experience with process validation including IQ, OQ, and PQ.
- Experience with manufacturing risk assessment and process controls.
- Demonstrated experience working with internal and external stakeholders.
- Experience managing project timelines and supporting multiple projects simultaneously.
- Experience working with cross functional teams and managing supplier changes.
- Experience supporting complex medical device manufacturing operations.
- Experience implementing new manufacturing methods and approaches.
- Experience with verification and validation activities within a regulated manufacturing environment.
- Experience driving continuous improvement initiatives.
- Manufacturing Engineering
- Class III Medical Devices
- Process Validation
- IQ OQ PQ
- Risk Assessment
- Process Controls
- Cross Functional Project Management
- Recruiter
- Phone
- Anwesha Mohapatra
- View email address on click.appcast.io
Vacancy posted 4 days ago
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