Manufacturing Engineer
28 Oct 2025
Verified by Turrior
Content + Source + Freshness • 13 Dec 2025 • 95% confidence
80 / 100
Offer value
Solid value due to demand for manufacturing engineers in the medical device sector and emphasis on compliance and process optimization.
- Positioned in a high-demand medical device sector.
- Opportunity for career growth through process optimization.
- Requires expertise and attention to regulatory detail.
Pros
- Positions the engineer at the forefront of medical technology.
- Opportunities for continuous improvement through Lean and Six Sigma.
- Clear expectations enhancing role clarity and commitment.
Cons
- Fast-paced environment that can be stressful at times.
- Onsite requirement may limit candidate reach.
- Compliance-driven, necessitating meticulous attention to detail.
Who it's for
Senior • Onsite
Good fit
- Experienced engineers in the medical device field.
- Professionals looking to excel in manufacturing engineering.
- Individuals focused on quality and compliance.
Not recommended for
- Entry-level candidates.
- Individuals seeking flexibility or remote work.
- Candidates not ready for a fast-paced work environment.
Motivation fit
Desire to innovate within manufacturing processes.Interest in applying Lean and Six Sigma methodologies.Commitment to quality assurance and regulatory standards.
Key skills
Process optimization and validation expertise.Lean and Six Sigma methodologies.Cross-functional teamwork and collaboration.Strong problem-solving and analytical skills.
Score: 80/100 AI verified analysis
About the job
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Manufacturing Engineer
Apply Location: Sylmar, CA(100% Onsite)Duration: 6+months
We are seeking an experienced Manufacturing Engineer to join our team and contribute to the development and improvement of Class III medical device manufacturing processes.
Immediate interviews are in progress - apply now or send your resume to benarjia@kipitusa.com
Required:
- Minimum 5–6 years of experience supporting Manufacturing Engineering in Class III medical device manufacturing.
- Hands-on knowledge of Process Validation (IQ/OQ/PQ), Risk Assessment, and Process Controls.
- Strong experience in Lean, Six Sigma, and GMP methodologies for manufacturing process optimization.
- Proven ability to manage multiple projects, supplier changes, and cross-functional collaboration to meet project timelines.
- Skilled in identifying and resolving technical issues, driving process improvements, and implementing corrective actions.
- Proficiency in working with internal and external stakeholders to support manufacturing and quality goals.
- Ability to anticipate and identify key issues, recommend effective solutions, and apply creative or novel approaches when precedents don’t exist.
- Strong understanding of manufacturing operations, technical leadership, and business objectives in a regulated environment.
- Experience conducting peer reviews for validation and verification activities.
- Bachelor’s degree in Mechanical, Electrical, or Software Engineering (or equivalent technical discipline).
