Manufacturing Controls Engineer II
4 weeks ago
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Our 114,000 colleagues serve people in more than 160 countries. Abbott Rapid Diagnostics is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.
We are currently seeking a Manufacturing Controls Engineer II to join our team in Scarborough, Maine. In this role, you will be responsible for supporting product development from concept through sustained manufacturing of FDA-regulated products. This includes completion of process development, equipment acquisition and leadership of supporting development partners.
Key Responsibilities- Process development, equipment specification, acquisition and implementation.
- Evaluation of machine logic and controls to troubleshoot equipment and identify process improvement opportunities.
- Integration of controls hardware and software into new and existing manufacturing equipment.
- Design of experiments, validation, completion of testing and analysis of data.
- Suggests and supports new methods or materials for continual improvement of quality and efficiency.
- Analyzes current equipment for process suitability and provides detailed plans for improvement.
- Bachelor's degree (BS) in engineering or equivalent combination of education and experience.
- Minimum 3 years engineering experience in a manufacturing environment.
- Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
- Ability to write reports, business correspondence, and procedure manuals.
- Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.
- Experience working in a GMP, FDA, ISO and USDA regulated environment.
- Familiarity with cGMP and ISO 13485 regulations and practices is desired.
- Familiarity with a variety of material testing and measuring methods.
Abbott is an equal opportunity employer and welcomes diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call or email.
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