Vacancy caducado!
Help us improve access to life-changing therapies that can transform human healthWe are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.We are looking for a Design Transfer Specialist to work with our expert Design Transfer team of 3 employees across the world. Do you have a passion for Design Control? Then we would love to hear from you. What you’ll doCoordinate and expedite the flow of product registrations. Plan and prioritize execution of registration activities. Ability to trouble shoot. Fully proficient professional, contributes to projects and initiatives, influences at the site level and determines and executes to operational standards and processes, and requires understanding of a concepts, methods and procedures. Work within all levels of the organization.The Registration Specialist will interface with all levels of the of the organization to execute registrations. The candidate must have the ability to manage and complete all work requirements with little to no management or intervention. New part registrations for Westborough site. Coordinate and follow-up on open tasks Oracle set up (Manufacturing database) Magic set up (Engineering database) Bill Of Material Structuring set up Trouble shooting Understanding of Supply Chain wing to wing process (Material lifecycle) Partner closely with sourcing Support MBL and EBL updates Purchase order set up Tools: Excel, Word,Qliksense, Sales Force Dot Com,Filesanywhere, Skilled Computer background Support all lean activities, initiatives, and action workouts Work on streamlining registrations (Simplification/Lean) Create Procedures Submit enhancement requests in Magic and Oracle to assist in automating registrations Work with Distribution sites to find ways to improve material flowWho you are
Associate degree from an accredited university or college (or a high school diploma / GED with at least 4 years of experience in Manufacturing)
Computer proficiency
Working knowledge of MRP (Material Requirement Planning)
Excellent Interpersonal Skills
Strong problem solving skills
Magic experience
Oracle knowledge and experience
Strong oral and written communication skills.
Strong interpersonal and leadership skills.
Ability to work independently.
Who we areWhatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Vacancy caducado!