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    Engineer, Device Development and Commercialization - Oklahoma City, United States - Kymanox

    Kymanox
    Kymanox Oklahoma City, United States

    4 weeks ago

    Default job background
    Description
    Engineer, Device Development and Commercialization

    You want to make a difference and have an impact...
    You enjoy having an influence in your day to day work...

    You are motivated by working alongside a team filled with subject matter experts that will help you learn and grow...

    You wake up every day and do what you do
    If this sounds like you, you've come to the right place.

    Job Description:
    Kymanox is hiring for an

    Engineer, Device Development and Commercialization

    for our Device Development and Combination Products projects.

    This is a mid-level role, seeking candidates with strong device development background in combination products and experience leading projects and complex project teams.

    This role will be based in Boston, MA.

    The position will be engaged in leading key aspects of Kymanox's engineering service offerings and supporting clients with a deep knowledge in combination products.

    Experience to include prefilled syringes, auto injectors, nasal devices, inhalers, and/or similar products.

    The role may serve as key interface for clients as subject matter expert (SME) and technical lead for various programs.

    Projects may include any of the following focus areas:
    Combination Product Development and Commercialization (all aspects)
    Design Controls (e.g., expert DHF support)
    Design Verification and Validation (V&V)
    Process Improvement and Troubleshooting
    Technology Transfer and Scale-Up
    Validation (e.g., Shipping, Process)
    Data Analysis, Including Statistical Analysis
    Regulatory Submission Authorship and Review
    Project Management Leadership and/or Support
    Technical Report Authorship, Review, and Formatting
    Manufacturing and Complaint Investigations
    Quality Management Systems (QMS) Support
    Process and Product Development (including design)

    Additional responsibilities can include:
    Serve as a Single Point-of-Contact (SPOC) on multiple projects as the technical lead representative.
    Review and approval of technically complex documentation to ensure technical competence to relevant local and federal regulations.
    Completion of gap assessments against industry regulations or standards
    Participation in regulatory body inspections or remediation efforts
    Authoring of response letters to regulatory bodies
    Development of policies or standard operating procedures
    Supply chain and vendor management strategy and compliance
    Training (internal and external)
    Technical Project management and meeting facilitation

    Desired Aptitude and Skill Set:
    Strong knowledge of ISO13485, ISO14971, CFR 820.30, and EU MDR
    Resourceful
    Extremely detail oriented
    Ability to work effectively with remote team members and/or direct reports
    Highly organized
    Self-directing, self-pacing
    Excellent written and oral English communication skills
    Understanding of own limitations
    Ability to solicit and utilize subject matter expert input
    Fast learner
    Pleasant and positive communication style
    Ability to motivate self, team members, and direct reports
    High energy level
    Excellent problem-solving skills
    Seasoned soft skills (i.e., high EQ)
    Team player
    Thrive in a fast-paced, growing, and dynamic work environment
    Technology savvy

    Required Educational Background:
    Bachelor's degree in Biomedical, Mechanical, or Chemical engineering, or other technical discipline from an accredited institution or equivalent.
    Continuing education or certificates in project management, six-sigma, statistics, engineering, quality, or regulatory affairs is desirable but not required.
    Consideration also given to advanced degrees (e.g., MEng, MS, PhD) where there is demonstrated utilization of advanced schooling.

    Experience:

    5+ years of experience in development and manufacturing in the pharmaceutical, biotechnology, and combination product sectors is required.

    A demonstrated level of medical device and biologic and/or drug experience is required; overall talent and ability to learn from Kymanox experts is ultimately more important than current experience for long-term success at the firm.

    .
    Experience with pre-filled syringes, auto pen injectors, co-packaged kits, and/or other combination product platforms is required
    Familiarity with risk management tools and applications
    Familiarity with data analysis tools and applications
    ____________________


    About Kymanox:
    Kymanox ('ki-mah-noks'), meaning Ideal Knowledge Transfer, advances life science innovation through insightful solutions and collaboration.

    We do this by accelerating the design and commercialization of modern medicines for our customers using integrated engineering, scientific, compliance, and project management solutions that are insightful, collaborative, and comprehensive.

    By building and supporting the development of modern medicines, Kymanox has proven, end-to-end solutions that are helping bring better Life Science Products to the market- and keep it there.

    We do all of this with heart and pride... because patients deserve better.
    Kymanox, founded in 2004, serves clients from Fortune 100 companies to virtual start-up companies all across the globe.

    Headquartered in Research Triangle Park, NC, we have US offices in Boston and Philadelphia, and since 2022 have expanded to Germany, Switzerland, and Israel.

    __________________


    Travel:
    Up to 10% travel domestically (primarily) and internationally may be necessary to support client work.
    The position may evolve over time and responsibilities will be added.

    Since Kymanox is a growing company, there will be ample opportunities for advancement – both within the currently defined role, with other groups, and roles to be defined in the future.

    Medical healthcare including dental and vision, short- and long-term disability, life insurance, matching 401(k) retirement plan, student loan payment assistance, and other benefits.

    Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.

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