• 18 Apr 2018 6:30 PM | Anonymous

    To apply send resumes to eric@d2dtech.net

    Data2Design Technologies is an acclaimed Technology Services company. We specialize in delivering Custom Healthcare Application Development Services rapidly and cost effective.


    The mid-level sensei facilitates and supports the direct transfer of Lean skills through facilitation and implementation of Rapid Process Improvement  Events/Workshops/Projects, and Value Stream Analysis. Primary goal is to enhance the knowledge, understanding and application of Lean principles and tools to front line staff, mid-level managers, and improvement staff.

    The mid-level sensei supports pre-work assessment required of all Value Stream and Lean RPIW/improvement events, reviews data/materials/documents for relevance, applicability, and appropriateness providing corrective guidance on how to conduct process and value stream maps. Provide facilitation and support of SIM deployment within each site.

    Required Skills and Experience:

    • Bachelor’s Degree OR equivalent work experience 

    • AND:

    • 5 or more years of providing consulting services to large-complex healthcare organizations.
    • Black Belt level certification (preferably from an American Society for Quality accredited institution).
    • Experience and ability to successfully teach Lean course materials to all levels of student knowledge and experience (beginning, intermediate, and advanced) to achieve course objectives.
    • Ability to plan, multi-task, and deliver services on schedule; ability to provide on-site support for work.

    Equal Opportunity Employer (EOE). Qualified applicants are considered for employment without regard to age, race, color, religion, sex, national origin, sexual orientation, disability, or veteran status.

  • 12 Apr 2018 11:30 AM | Anonymous

    When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

    How will you make an impact?

    Our commitment to quality is at the heart of our brand and is vital to our growth and success. This key role is responsible for working with the Leadership team to build a Quality vision that’s aligned with the business strategy of our fast growing and evolving Genetics Sciences Division (GSD).

    In Genetic Sciences we are moving from a life sciences tools provider to a genetic solutions leader with best-in-class systems and expanded content and applications that meet the diverse needs of our global customer base. The stories we tell in GSD are some of the most compelling and inspirational as any in our company and as we continue to push further into the clinic and make our plaforms accessible to more and more customers they will not only be the stories we tell but what the world is talking about. ​

    What will you do?
    • Build and drive a Quality vision and strategic objectives that aligns with our Genetic Sciences Division and Life Sciences Group operations.
    • Lead and inspire a strong global quality team by hiring and developing strong quality leaders, establishing and actively managing performance expectations, and providing development and training opportunities.
    • Coach and motivate a global Quality Assurance team with a mix of RUO (ISO 9001), HID, CE-IVD (13485), and GMP (21CFR820).
    • Drive operational excellence by effectively using continuous improvement skills and tools to prioritize and drive projects and improvements/standardization across the network to improve Quality service levels, reduce costs, and align with strategic objectives.
    • Establish network wide QA/QC priorities and key objectives to reduce turnaround time, the cost of poor quality and improve the compliance to regulations and the site Quality Management System.
    • Ensure global training is effective and that the plants operate within the required regulatory guidelines.
    • Influence and build strong working relationships across organizations and geographies and engage with business partners to define existing gaps and future requirements for Quality Management Systems.
    • Ensure effective management of the network / site Quality Management System including assuring effective management reviews, complaint handling, CAPA system, change control, calibration maintenance, process validation, internal auditing, R&D transfers, and manufacturing area support.
    • Drive the continuous improvement of Quality Management Systems at sites around the world, including assuring effective management reviews, complaint handling, CAPA system, change control, calibration maintenance, internal auditing, R&D transfers, validation, and manufacturing area support.
    • Support the commercialization of New Product Introductions by working with Design Compliance team members.
    • Collaborate with the Global Regulatory organization to ensure compliance to applicable regulations.
    • Lead executive quality management reviews.
    How will you get there?

    • Bachelor’s degree in Science or Engineering Disciplines.
    • A minimum of 10 years of Quality experience within the Medical Device, Pharmaceutical Industry or Clinical Testing industry.
    • Decisive leader who’s successfully managed larger teams in a highly matrixed organization.
    • Demonstrated experience working with external customers and commercial teams creating strategies that address customer needs and product specification.
    • Previous experience working global teams and applying global business acumen.
    • Proven experience with Project Management and Lean Six Sigma methodology.
    • Previous experience supporting Medical Device or Pharmaceutical New Product Introductions preferred.
    Knowledge, Skills, Abilities
    • Customer focus – Puts the customer at the front of every decision, including work prioritization, resource investment, and process improvement
    • Quality systems – Ability to practically implement strong quality systems that provide only the necessary controls as defined by marketplace and our customers
    • Transformation – Understand the levers necessary to elegantly transform a traditionally research based business to a mixed research and clinically focused business
    • Building a team – Builds a strong team and has a strong capability marry strategy, organizational structure, and talented leaders
    • Operational execution – Clear view of the mechanisms necessary to manage a global quality organization efficiently and effectively
    • Ability to travel up to 50%

    This position has been approved for relocation assistance.

    To Apply Online: http://jobs.thermofisher.com/ShowJob/Id/78434/Senior-Director-of-Quality/

    About Thermo Fisher Scientific
    Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of more than $20 billion and approximately 65,000 employees globally. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory productivity. Through our premier brands – Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services – we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive services.
Powered by Wild Apricot Membership Software