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    Manufacturing and Automation Mechanical Engineer - Fort Lauderdale, FL, United States - Jobot

    Jobot
    Jobot Fort Lauderdale, FL, United States

    3 weeks ago

    Jobot background
    Description
    Amazing Pharmaceutical R&D and Product Development Opportunity
    This Jobot Job is hosted by: We represent a US-based, development-stage biopharmaceutical company headquartered in Weston, Florida.

    The mission of the company is to harness the power of inhaled drug delivery to improve patient access to important therapies and develop treatments for serious diseases where therapeutic options are significantly lacking.

    Dental insurance
    Responsible for device engineering activities in the context of pharmaceutical research and development (R&D).

    The device engineer will be responsible for commercial manufacturing processes including semi-automated to automated and large-scale manufacturing and assembly operations.

    The device engineer will utilize industry standard and novel equipment, processes, and methodologies to transform raw materials, components, and parts into finished goods to the required standards of safety, quality, cost and delivery across supply chain channels.

    The device engineer will be responsible for developing, maintaining, and optimizing the supply chain with a keen eye for cost of goods (COGS) as applicable to raw material, manufacturing processes and overall supply chain.

    The device engineer will interface with early device design teams and be responsible for independently providing direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals.

    Lead and execute manufacturing activities of devices with a focus on orally inhaled and nasal drug products (OINDPs).
    ~Responsible for developing and implementing best practices for manufacturing commercial products.
    ~Develop, propose, and implement vision, strategy, policies, processes, and procedures to aid and improve business performance.
    ~Lead and execute technical analyses including statistical analysis and tolerance analysis.
    ~Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
    ~Interface and lead activities with third party contract research, development, and manufacturing organizations.
    ~Ensure that manufacturing strategies and processes are in place to meet business objectives and operational needs in terms of price, quality, and delivery targets and that enable the organization to function and compete effectively in the market.
    ~Proactively evaluate the challenges faced by the business and take actions to mitigate risks and develop opportunities.
    ~Document standard operating procedures (SOPs) for design controls and manufacturing in the context of pharmaceutical drug-device combination products.
    ~Provide project updates/reporting through program governance.
    ~and phase appropriate guidelines and policies.
    ~Execute project strategy, priorities, and milestones ensuring visibility and accountability.
    ~Proactively lead with integrity and engage cross functional project teams and stakeholders.
    ~Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

    S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 6 to 9 years, B.S. with 12 to 16 years device development experience in pharmaceutical or related field.
    ~Experience with device development and manufacturing in the context of pharmaceutical R&D and product development is a must to have.
    ~Must possess expert knowledge and experience with commercial scale device manufacturing and assembly processes including manual, semi-automated and/or commercial scale automated processes.
    ~Must possess expert knowledge of manufacturing processes including injection molding and metal machining processes.
    ~Must possess expert knowledge of mechanical design with preference for SolidWorks.
    ~Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
    ~Strong English language skills including writing ability and oral communication.
    ~
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