LifeSprout
Manufacturing Technician Job at LifeSprout in Baltimore
LifeSprout, Baltimore, MD, US
Job Description
Job Description
Position: Manufacturing Technician
Position Overview:
The Manufacturing Technician will be responsible for following established manufacturing
protocols to produce in-process material, components, and finished medical devices. They will also
be responsible for following Good Manufacturing Practices (GMP) as it relates to stringent
documentation of procedures performed.
Responsibilities:
Eligibility to work in the U.S. is required.
Position Overview:
The Manufacturing Technician will be responsible for following established manufacturing
protocols to produce in-process material, components, and finished medical devices. They will also
be responsible for following Good Manufacturing Practices (GMP) as it relates to stringent
documentation of procedures performed.
Responsibilities:
- Produce composite materials using electrospinning, cryomilling, plasma treatment, and chemical processes.
- Assist in collaborative research projects with other team members.
- Create and refine work instructions and inspection procedures.
- Design and conduct manufacturing investigations and trend analysis for trouble-shooting manufacturing concerns.
- Conduct process validation investigations that confirm reproducibility, scale-up potential, and ongoing quality assurance with manufacturing procedures.
- Undergraduate degree in chemistry, chemical engineering, materials science, biomedical engineering, or a related discipline with 0-2 years of experience in industry or academia or 2+ years in a medical device or pharmaceutical industry manufacturing environment.
- Experience in materials processing and machine operation; beneficial if previous experience includes electrospinning, hydrogel synthesis, and/or surface modification.
- Demonstrated ability to execute on deliverables and manage milestones.
- Previous experience working with work instructions and inspection procedures/processes, specifically within a cleanroom setting.
- Previous experience in handling investigations, trend analysis, and/or CAPA analysis.
- Working knowledge of GMP manufacturing processes, FDA and regulatory bodies, and quality systems.
- Specific work or academic project experience in the soft tissue aesthetic and/or reconstructive arenas
Eligibility to work in the U.S. is required.
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