Embarking on a career in the mechanical trade in Thousand Oaks, CA, often begins with an apprenticeship, combining hands-on experience with classroom learning, allowing individuals to earn while they learn. Apprenticeships typically last three to four years, requiring extensive training under licensed professionals. According to the U.S. Bureau of Labor Statistics, the mechanical trade sector employs approximately 19,753 professionals in Thousand Oaks, with wages averaging around $1,798 per week. The trade offers strong earning potential, with experienced mechanical professionals often exceeding $89,000 annually. Trade schools, apprenticeship programs, and industry associations provide pathways to enter this growing field, offering a stable and lucrative career opportunity.
Job Description We are seeking an experienced Mechanical Engineering Professional to join our team at Savvy, Inc. in Thousand Oaks, CA. About the Role This position requires strong experimental, analytical, and statistical skills to support technical operations and ensure the success of the combination product portfolio. Key Responsibilities • Designing, developing, and testing mechanical components of drug delivery devices. • Analyzing test data and applying statistical methods to derive actionable insights and recommendations. • Leading testing efforts to assess and validate proposed modifications to existing devices. • Collaborating with cross-functional teams to develop and implement new product designs. • Maintaining accurate records of testing and validation activities. • Ensuring compliance with regulatory and quality requirements for combination products and medical devices. Requirements • A degree in Mechanical Engineering or a related field. • Experience in laboratory testing and experimentation. • Knowledge of statistical tools and methodologies. • The ability to work collaboratively in a fast-paced environment. • Strong communication and problem-solving skills.
See More Details >>Payrate: $40.00- $43.00 /hr Job Description: The Device Engineer will participate in the medical device/combination product design, development, and commercialization activities for drug delivery devices, focusing on prefilled syringes. Key responsibilities include: Leading test procedure development and functional test execution Leading material inventory management for prefilled syringe programs, including material forecasting and material custody across multiple sites and functional groups. Authoring technical plans and reports Performing advanced statistical data analysis Supporting Leading technical assessments and root cause investigations as well as planning and delegation of sub-tasks to other team members. Transfer of information to manufacturing sites, engagement with suppliers Maintenance of Design History File content consistent with Good Documentation Practices Training junior staff on physical test methods, sample preparation protocols and procedures, and effective report writing. Reviewing primary data collected from peers in support for various design controls activities, including characterization and design verification. Supporting design transfer activities by leading cross-functional coordination of sample procurement and testing. Supporting the setting of specification limits for platform devices through human factors studies benchtop testing. Essential Skills: Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments. Plans and conducts work requiring judgment in the independent evaluation, selection, and adaptation and modification of standard techniques/procedures/criteria, and devises new approaches to encountered challenges. Generates and maintains design specifications, protocol and report writing, prototyping, design of experiments/statistical process control product optimization, design verification & validation, FMEA, etc. System level root cause investigation; CAD/SolidWorks proficiency; tolerance analysis; capability analysis. Coordinate and implement design improvements with development partners. Collaborate with scientists and engineers internally and externally to assess and develop appropriate design and manufacturing specifications. Accountability of maintaining technical records within product design history files. Individual contributor with leadership attributes to effectively represent device engineering within a large network/matrix organization. Working proficiency and familiarity with governing standards and regulations, including Quality System Regulation (21CFR820) and Risk Management (ISO 14971). Preferred Qualifications: Degree in the field of Mechanical or Biomedical Engineering, or related field Medical device industry and/or regulated work environment experience Excellent written and verbal communication skill Understanding and experience in: Development/commercialization of medical devices and knowledge of manufacturing processes Initiating and bringing complex projects to conclusion Ability to work independently and dynamic cross functional teams Design controls Failure investigation Applied statistics Basic Qualifications Doctorate degree OR Master degree and 3 years of experience OR Bachelor degree and 5 years of experience OR Associate degree and 10 years of experience OR High school diploma / GED and 12 years of experience Top 3 Must Have Skill Sets: Pharma background. Physical testing experience Design controls experience Pay Transparency: The typical base pay for this role across the U.S. is: $40.00 - $43.00/hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance. For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy (https://www.aditiconsulting.com/privacy-policy). Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions. By applying to this position, you agree to Aditi’s use of AI technology including calls from an AI Voice Recruiter. #AditiConsulting Payrate: $40.00- $43.00 /hr Job Description: The Device Engineer will participate in the medical device/combination product design, development, and commercialization activities for drug delivery devices, focusing on prefilled syringes. Key responsibilities include: Leading test procedure development and functional test execution Leading material inventory management for prefilled syringe programs, including material forecasting and material custody across multiple sites and functional groups. Authoring technical plans and reports Performing advanced statistical data analysis Supporting Leading technical assessments and root cause investigations as well as planning and delegation of sub-tasks to other team members. Transfer of information to manufacturing sites, engagement with suppliers Maintenance of Design History File content consistent with Good Documentation Practices Training junior staff on physical test methods, sample preparation protocols and procedures, and effective report writing. Reviewing primary data collected from peers in support for various design controls activities, including characterization and design verification. Supporting design transfer activities by leading cross-functional coordination of sample procurement and testing. Supporting the setting of specification limits for platform devices through human factors studies benchtop testing. Essential Skills: Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments. Plans and conducts work requiring judgment in the independent evaluation, selection, and adaptation and modification of standard techniques/procedures/criteria, and devises new approaches to encountered challenges. Generates and maintains design specifications, protocol and report writing, prototyping, design of experiments/statistical process control product optimization, design verification & validation, FMEA, etc. System level root cause investigation; CAD/SolidWorks proficiency; tolerance analysis; capability analysis. Coordinate and implement design improvements with development partners. Collaborate with scientists and engineers internally and externally to assess and develop appropriate design and manufacturing specifications. Accountability of maintaining technical records within product design history files. Individual contributor with leadership attributes to effectively represent device engineering within a large network/matrix organization. Working proficiency and familiarity with governing standards and regulations, including Quality System Regulation (21CFR820) and Risk Management (ISO 14971). Preferred Qualifications: Degree in the field of Mechanical or Biomedical Engineering, or related field Medical device industry and/or regulated work environment experience Excellent written and verbal communication skill Understanding and experience in: Development/commercialization of medical devices and knowledge of manufacturing processes Initiating and bringing complex projects to conclusion Ability to work independently and dynamic cross functional teams Design controls Failure investigation Applied statistics Basic Qualifications Doctorate degree OR Master degree and 3 years of experience OR Bachelor degree and 5 years of experience OR Associate degree and 10 years of experience OR High school diploma / GED and 12 years of experience Top 3 Must Have Skill Sets: Pharma background. Physical testing experience Design controls experience Pay Transparency: The typical base pay for this role across the U.S. is: $40.00 - $43.00/hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance. For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy (https://www.aditiconsulting.com/privacy-policy). Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions. By applying to this position, you agree to Aditi’s use of AI technology including calls from an AI Voice Recruiter. #AditiConsulting
See More Details >>RKS has been at the forefront of Industrial Design in the United States for the last 40 years. We have crafted a reputation for our complete product design and development service; bringing innovation that enhances every-day lives across all market sectors, from sporting goods to dental devices, from wearables to household appliances. Our approach puts innovation, engineering, and user experience at the center of our process, creating ground-breaking products that consumers bond with and clients keep coming back for. We are seeking an experienced team member to join our engineering and product development team. Candidates are sought with at least five years' experience, (ten years a plus) in the field of engineering and developing consumer, commercial and medical products, working on all aspects of the product development life cycle, from development strategies, through fast-fail prototypes, engineering concept development, and ultimately designing complex assemblies in collaboration with electronics engineers and industrial designers to create complete engineering packages for manufacturing. RKS team members flourish under pressure and enjoy the opportunity to wear many different hats in a highly collaborative, creative studio that believes in creating the very best. Project Management and Execution • Lead Complex Projects: Oversee the technical aspects of complex engineering projects from conception to completion. • Resource Allocation: Efficiently allocate resources and manage timelines to ensure project milestones are met. • Quality Assurance: Ensure engineering solutions meet both client specifications and industry standards. • Risk Management: Identify and mitigate risks associated with project engineering. • Client Interaction: Act as a primary technical point of contact for clients, providing updates and addressing concerns. Technical Expertise and Innovation • Design and Development: Create and refine mechanical designs that are innovative, cost-effective, and technically sound. • Problem Solving: Tackle complex engineering challenges, applying advanced principles of mechanical engineering. • Research and Analysis: Conduct research to stay abreast of the latest technology trends and apply them to current projects. • Prototyping and Testing: Oversee the development of prototypes and conduct rigorous testing to validate designs. • Documentation: Maintain comprehensive documentation of design processes and engineering decisions. Team Leadership and Mentorship • Mentoring: Provide guidance and mentorship to junior engineers and other team members. • Team Collaboration: Foster a collaborative environment, encouraging input and feedback from various team members. • Skill Development: Identify training opportunities for team members to enhance their engineering skills. • Performance Reviews: Conduct regular performance evaluations and provide constructive feedback. • Conflict Resolution: Address and resolve any interpersonal or technical conflicts within the team. Process Improvement and Standards Compliance • Workflow Optimization: Streamline engineering processes for efficiency and effectiveness. • Standardization: Ensure compliance with industry standards and best practices in mechanical engineering. • Innovative Solutions: Implement innovative processes and tools to enhance engineering workflows. • Regulatory Compliance: Keep abreast of and ensure adherence to relevant laws, regulations, and guidelines. • Sustainability: Advocate for and incorporate sustainable and eco-friendly engineering practices. Communication and Reporting • Technical Reporting: Prepare and present detailed engineering reports to stakeholders. • Cross-Departmental Liaison: Coordinate with other departments (like UI/UX, research, and strategy) to align engineering solutions with overall project goals. • Presentation Skills: Effectively communicate complex technical information to non-technical audiences. • Feedback Integration: Incorporate feedback from clients and stakeholders into ongoing project work. • Documentation: Ensure thorough and accurate documentation of all engineering processes and decisions. Requirements MINIMUM QUALIFICATIONS • Five years' experience, (ten years a plus) in the field ofengineering and developing consumer and medical products • A minimum of a Bachelors degree in Mechanical Engineering orProduct Design Engineering is required for this position. • Candidates must demonstrate aptitude for rapid creation ofinnovative mechanical solutions (structures andmechanisms) • Familiar with all common prototyping and manufacturingmaterials and processes • Highly experienced with SolidWorks best practices in solidmodelling, surface modelling, assemblies, drawings and design for manufacture PREFERRED QUALIFICATIONS • Client-facing, project management experience ishighly preferred • Consulting / Agency experience is highlypreferred • Experience with medical product development aplus • Experience with electronics integration is preferred Benefits • Medical Insurance • Dental Insurance • Paid holidays • 401 K as defined in the employee handbook • Sick leave • Vacation
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