Scientist II

Job description

Position Overview:

Are you the right scientist to work in a fast-paced manufacturing environment with cross-functional focus?  Would you enjoy working on a team developing one culture based on trust, accountability, ownership, and world class performance? We are looking for a candidate to join our Quality Control team who will be involved in supporting a newly established reagent manufacturing system as well as future integration projects within an Immunoassay product line. Come join our team and embrace the Siemens belief of “Know now, live better…”

 

Major Job Responsibilities

·  Performs routine and moderate to complex tests and analyses according to established procedures
·  Performs complex tests or investigations pertaining to the development of new designs, methods, materials, or processes and investigates possible application of results.
·  Performs release activities and inputs associated data into SAP.
·  Troubleshoots and resolves complex problems.
·  Completes a wide variety of complex technical assignments.
·  Obtains, correlates, and analyzes technical information needed to accomplish semi-complex tasks.
·  Completes the preparation of reports, charts, graphs, and other documents and advises senior staff.
·  Reviews and approves related inputs such as complex drawings and specifications prepared by technical support personnel.
·  Coordinates with engineering support to arrange for the production of complex experimental runs or for the construction of experimental models and special test equipment.

 

Required Knowledge/Skills, Education, and Experience

·  B.A. or B.S. Degree in biology, chemistry or another science related field.
·  3 years of successful experience in quality processes and quality technical support of quality related processes and systems.
·  Experience working with analytical instrumentation, reagent systems, including testing repetitively.
·  Experience performing data analysis as well as formal report writing.
·  Experience creating and modifying testing protocols and supporting documents.
·  Familiar with statistical analysis tools.
·  Strong scientific, communication and organizational skills are a must.
·  Should be comfortable with handling bio-hazardous materials.
·  Thorough understanding of 21 CFR Part 820 regulations and ISO 13485 standard requirements, and all other MDSAP country regulations for medical device or pharmaceutical operations.

 

 

Preferred but not Required

·  Experience with immunoassay-based technologies, specifically involving cardiac based assays.
·  Familiar with working in SAP.

 

Organization: Siemens Healthineers

Company: Siemens Healthcare Diagnostics Inc.

Experience Level: Experienced Professional

Job Type: Full-time

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