Jobs via Dice
Manufacturing Engineer (Medical Device)
Jobs via Dice, Los Angeles, California, United States, 90079
Overview
Dynamic Enterprise Solutions Inc is seeking a Manufacturing Engineer, Special Projects in Los Angeles, CA. Apply via Dice. Responsibilities
Support Manufacturing Engineering in a class 3 medical device environment. Apply manufacturing methodologies (e.g., lean, Six Sigma, GMP) as appropriate. Knowledge of Process validation (IQ/OQ/PQ); risk assessment; and process controls. Work with internal and external stakeholders across projects. Manage project timelines and coordinate across cross-functional teams. Support supplier changes and multiple concurrent projects. Qualifications
Minimum 5–6 years of experience in supporting Manufacturing Engineering in a class 3 medical device context. Experience with process validation (IQ/OQ/PQ), risk assessment, and process controls. Experience collaborating with internal and external stakeholders. Experience managing project timelines, cross-functional teams, and supplier changes. Class 3 medical device experience is required. Location
Los Angeles, CA (locations in listings include Los Angeles and Hawthorne, CA) Note
Other boilerplate, referral prompts, and non-essential postings have been removed for clarity. This description preserves the original role information without adding new facts.
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Dynamic Enterprise Solutions Inc is seeking a Manufacturing Engineer, Special Projects in Los Angeles, CA. Apply via Dice. Responsibilities
Support Manufacturing Engineering in a class 3 medical device environment. Apply manufacturing methodologies (e.g., lean, Six Sigma, GMP) as appropriate. Knowledge of Process validation (IQ/OQ/PQ); risk assessment; and process controls. Work with internal and external stakeholders across projects. Manage project timelines and coordinate across cross-functional teams. Support supplier changes and multiple concurrent projects. Qualifications
Minimum 5–6 years of experience in supporting Manufacturing Engineering in a class 3 medical device context. Experience with process validation (IQ/OQ/PQ), risk assessment, and process controls. Experience collaborating with internal and external stakeholders. Experience managing project timelines, cross-functional teams, and supplier changes. Class 3 medical device experience is required. Location
Los Angeles, CA (locations in listings include Los Angeles and Hawthorne, CA) Note
Other boilerplate, referral prompts, and non-essential postings have been removed for clarity. This description preserves the original role information without adding new facts.
#J-18808-Ljbffr