Sr. Design Transfer Engineer

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Full-Time Professional Eden Prairie, MN, US 4 days ago Requisition ID: 2506 Salary Range: $110,000.00 To $130,000.00 Annually Annual CIP bonus opportunity of up to $13,000.00 Responsibilities Serves as a lead core team member of a cross functional project team whose responsibilities include conducting studies directed toward the development of processes Performs standard scientific assignments to evaluate results for validity and conformance to acceptable scientific methods. Independently determines requirements and acceptance criterion associated with testing performed. Applies deep knowledge of six sigma methodologies (process capability, SPC, etc.) to assess product design and translate them into process specifications Participates and consults with the internal and external scientific community to maintain a state-of-the-art knowledge for application to achieving successful experimental outcomes Deploys deep knowledge of manufacturing to suggest and implement creative solutions in process development and test method creation innovating manual hand driven processes to semi-automated equipment driven processes. Coordinates or performs validations and documents risk management activities to support regulatory submissions or product launches Leverages expertise across projects and specialties to effectively accomplish assignments and identify and mitigate risks within a project. Leverages clinical and technical expertise to evaluate design and process risks and implement effective mitigation measures Exhibits functional autonomy through creating project direction assigning design transfer deliverables required to support both new product development projects and design change projects Reviews and edits internal documentation for team members and assists in the preparation and presentation of materials for internal or external technical reviews May serve as a team lead and have direct reports Supports Quality process improvement initiatives Education Bachelor’s degree in relevant area Experience 6+ years of relevant medical device, pharmaceutical, or other regulated industry experience Certification N/A Skills Strong attention to detail and documentation practices Ability to work independently in a small-company environment Effective communication and cross-functional collaboration Problem-solving and investigative mindsetStrong knowledge of microbiological techniques and aseptic processing Travel N/A Physical Requirement Move or lift objects up to 25 pounds Frequent (>75%) stationary position (standing or sitting) while utilizing digital displays Frequent (>75%) fine manipulation using hands and fingers (typing, opening, writing, clicking, paper sorting, etc.) Onsite: Office environment with assigned workstation Remote positions only: Home office environment with minimum distractions #J-18808-Ljbffr Evergen