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Location
In office (Maple Plain)
Seniority
Senior · 7+ years exp
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H-1B filings in 12 months: 2
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Contractor

Confirmed on the employer's own hiring board on Nov 10, 2026. First seen by Alion on Oct 30, 2026. Planet Pharma scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Planet Pharma is a life sciences recruitment and staffing firm headquartered in Deerfield, Illinois, that places contract and permanent professionals with pharmaceutical, biotechnology, medical device and contract research organizations. Founded in 2012, it offers contract and direct hire staffing, strategic resourcing, executive search, functional service provider models and global workforce solutions, with offices in Deerfield, Chicago and Raleigh and placements in the United States, Europe and Asia. Planet Pharma recruits for clients research scientists and associates, clinical trial managers, quality engineers, compliance specialists, medical writers and production supervisors.

Pay Range: 27-37/hr

*depending on exp

Description:

This is an exciting opportunity for a well-rounded engineer to join a small team supporting a recently acquired medical device startup. As a Manufacturing Engineer, you will support the development, validation, and scale-up of manufacturing processes for our innovative surgical device - directly contributing to product quality, efficiency, and patient outcomes. In all actions, the Manufacturing Engineer will demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented processes and procedures

Manage special projects and initiatives as assigned, driving them from planning through implementation and final completion

Lead development and optimization of manufacturing processes for soft-tissue repair device systems

Drive design for manufacturability (DFM) and transfer of robust processes into high-volume production

Develop and validate equipment, fixtures, and tooling for assembly and inspection

Partner cross-functionally with R&D, Quality, and Supply Chain to resolve technical issues and improve output

Execute structured root-cause analysis and corrective actions for production challenges

Support process validations, change controls, and documentation in compliance with ISO 13485/FDA QSR

Skills:

7-10+ years engineering experience in manufacturing or process engineering, understand manufacturing metrics and continuous improvement tools (e.g., lean, DMAIC)

Have hands-on experience scaling products from prototype to production is a benefit, skilled in fixture/tooling design and implementation

Strong CAD and problem-solving skills

Familiarity with regulated medical device environments

Strong problem-solving skills, attention to detail, self-starter with proven ability to successfully work with minimal supervision, good teamwork and interpersonal skills, good written and verbal communication, ability to multitask, prioritize, and meet project deadlines with high attention to detail

SolidWorks proficiency desired

familiarity with 5s and DMADV

Physical Demands:

Ability to lift up to 30 pounds

Must be able to wear clean room clothing and work in a cleanroom environment as needed

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