Laboratory Technician

Siemens Healthineers

1d•$46,040 - $63,305•Onsite

About The Position

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. The Manufacturing Technician I - Standards position plays a key role for the Standards Manufacturing team at the Siemens East Walpole facility. This position will execute Laboratory Diagnostic Manufacturing in the Standards and Controls Manufacturing Work Center. Reporting to the Senior Supervisor of Manufacturing-Bulk Formulation, the primary functions of the Manufacturing Technician I position are to; Formulate, Tests, and Release, all Control System materials for Centaur and Atellica assays produced in Walpole Manufacturing Facility, maintain cGMP compliance and adherence to site SOP’s, track and maintain raw material inventory, testing supplies, and operating supplies within the Standards Manufacturing Laboratory. This position includes the handling of all types of materials, including hazardous and DEA (Drug Enforcement Agency) controlled materials. The successful candidate must pass a DEA background check. This is a role well suited to an ambitious professional, looking for the next step in their career. As a Manufacturing Technician I - Standards, you will be responsible for:

Requirements

BS/BA in related discipline, or an AS/AA with a focus on the sciences, or equivalent combination of education and experience
0-2 years’ experience working in a similar role in the medical diagnostic/ medical device industry
Excellent organization and time management skills
Excellent laboratory technique
High attention to detail and commitment to accuracy
Excellent communication skills both verbal and written
Ability to lift up to 50 pounds
Ability to work individually and in a team setting
Must pass a Drug Enforcement Agency (DEA) background check

Nice To Haves

Working knowledge of cGMP requirements
Prior experience manufacturing commercialized automated immunoassays and/or ELISA and chemiluminescent products
Proficiency with Microsoft Office applications
Prior knowledge and use of SAP or similar MRP/ERP system

Responsibilities

Manufacturing Siemens Control System materials using established Manufacturing protocols and procedures
Running and interpreting In-Process testing on Control System materials using established Quality Control protocols and procedures.
Demonstrating Proficiency running and maintaining Testing Equipment within the Standards Manufacturing Lab.
Generating manufacturing documentation including Manufacturing Batch Records, Bills of Materials, Routings, Process Documents and SOP’s
Identifying and initiating continuous improvement activities in line within the Healthineers Performance System (HPS) framework
Participating in Continuous Improvement activities
May be asked to temporarily assume higher level responsibilities on a limited basis with direct support from Senior Supervisor of Manufacturing