Intellectt Inc
Role: Microbiologist
Location: Plymouth, MN 55442
Duration: 1-year contract minimum; small chance of conversion to FTE.
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What You’ll Do: A Sterilization Microbiologist to support the transition of subassemblies and finished goods from internal manufacturing to third-party manufacturers. Must have strong ethylene oxide sterilization expertise, including validation and product adoption. Serve as the microbiology/sterilization lead on multiple project teams. Assess third-party manufacturing spaces for microbiological quality. Document sterilization adoption into validated ethylene oxide cycles. Perform and oversee sterilization validations. Provide technical writing for project deliverables. Minimal supervision once trained.
What we are looking for: Ethylene oxide sterilization expertise (validation and product adoption) Strong microbiology background in a manufacturing setting Technical writing skills Independent, self-directed work style 5+ years relevant experience (medical device or pharma acceptable) Experience contributing data for regulatory submissions Knowledge of manufacturing space assessments for microbiological quality Previous experience in product transfers to third-party manufacturers Bachelor’s or Master’s degree in a scientific discipline preferred (biology, microbiology, chemistry). Open to other degrees if candidate has strong relevant experience. 5+ years in microbiology and sterilization (ethylene oxide required). Experience may come from medical device or pharma. Technical writing experience required. Regulatory submission experience a plus, but not required. Top skills: Ethylene oxide sterilization & validation expertise. Microbiology in a manufacturing environment. Strong technical writing skills. Independent work style. Ability to travel occasionally (possible destinations include Costa Rica).
Scroll down to find an indepth overview of this job, and what is expected of candidates Make an application by clicking on the Apply button.
What You’ll Do: A Sterilization Microbiologist to support the transition of subassemblies and finished goods from internal manufacturing to third-party manufacturers. Must have strong ethylene oxide sterilization expertise, including validation and product adoption. Serve as the microbiology/sterilization lead on multiple project teams. Assess third-party manufacturing spaces for microbiological quality. Document sterilization adoption into validated ethylene oxide cycles. Perform and oversee sterilization validations. Provide technical writing for project deliverables. Minimal supervision once trained.
What we are looking for: Ethylene oxide sterilization expertise (validation and product adoption) Strong microbiology background in a manufacturing setting Technical writing skills Independent, self-directed work style 5+ years relevant experience (medical device or pharma acceptable) Experience contributing data for regulatory submissions Knowledge of manufacturing space assessments for microbiological quality Previous experience in product transfers to third-party manufacturers Bachelor’s or Master’s degree in a scientific discipline preferred (biology, microbiology, chemistry). Open to other degrees if candidate has strong relevant experience. 5+ years in microbiology and sterilization (ethylene oxide required). Experience may come from medical device or pharma. Technical writing experience required. Regulatory submission experience a plus, but not required. Top skills: Ethylene oxide sterilization & validation expertise. Microbiology in a manufacturing environment. Strong technical writing skills. Independent work style. Ability to travel occasionally (possible destinations include Costa Rica).