Continuous Improvement Specialist III

at  Thermo Fisher Scientific

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. And you’ll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.
Fisher Clinical Services, part of Thermo Fisher Scientific, is a leading provider of global clinical supply chain. With unwavering commitment to service, science and process engineering, Fisher Clinical Services is powered by people with an exceptional commitment to quality, deeply instilled ethics of personal responsibility and unrivaled expertise. We are exclusively focused on serving the packaging and distribution requirements of clients across the world. Whether planning, packaging, labeling, storing, or distributing important supplies, Fisher Clinical Services has been committed to delivering the highest possible value while ensuring adherence to the highest level of quality, performance, reliability and sustainability standards. http://www.fisherclinicalservices.com/

KNOWLEDGE, SKILLS, ABILITIES

• BA/BS degree from an accredited college or university and 2+ years of Continuous Improvement related work experience
• Proficient knowledge and experience of Microsoft applications and supporting programs including (Outlook, Word, Excel, PowerPoint).
• Proficient knowledge and experience with GPM - the Fisher Global Project Management system and TrackWise (deviations, CAPAs, observations and change controls).
• Must have the ability to handle multiple projects and assignments and the ability to manage work schedules, project and task priorities.
• Must be results oriented, comfortable training and coaching others, and have the ability to communicate effectively up and down the organization.
• Preference given to employees with experience and/or certifications in Lean Manufacturing, Six Sigma and/or PPI (Practical Process Improvements)
• Mastery of skills required to read, understand, and adhere to the SOPs and policies of a GMP environment.

PHYSICAL REQUIREMENTS

• Must be able to physically perform duties of position which include: Exert up to 20 lbs. of force occasionally, and/or up to 10 lbs. of force frequently, and/or a negligible amount of force constantly to lift, carry, push, pull or otherwise move objects. Position usually requires walking or standing to a significant degree. May need to stoop, reach, or bend.

The individual will create/update SOPs as required for evolving processes, for audit observations, corrective and preventative actions, and to maintain compliance with periodic reviews.They assist in problem solving for the operations team related to resolving second level rooms on hold and/or GPM issues. Complete protocol requests, deviation investigations, change controls and corrective/preventative actions in the specific time frame. Establishes a solid focus on long-term continuous improvement activities through interaction with the entire Packaging Team staff.