We at Siemens Healthineers? are committed to helping healthcare providers globally to succeed in today’s dynamic environment. We are inspired to transform the way things are done – because we want what is best for our people, our customers and ultimately the health of mankind. While we are invested in engineering excellence – leading-edge medical technologies and services, we don’t stop there. We’re also deeply invested in our 46.000 people with the hearts of pioneers and minds of engineers, highly committed and connected in this industry. And as we strive to shape the future of healthcare, our overall success will depend on our ability to continuously reinvent ourselves.

If you are ambitious and change makes you thrive, help transform Siemens Healthineers into a learning organization.

This supervisor position will be responsible for the day to day operations for the filling and packaging for the Immune Assay product line, as a part of the Production department for the new China manufacturing facility.
Key deliverables are to meet product demand requirements, and to drive improvement in production processes and ensure effective training is provided to further reduce the potential for process error. The attributes necessary for success include the capability to lead, communication skills, interpersonal skills, attention to detail, time management, and drive.
?Engage in team buiding up, including hiring, training, supervision and qualification of Pack/Fill personnel to meet position requirements.
?Direct supervision and management of the Pack/Fill group personnel.
?Detailed written documentation of work, creation, update and maintain SOPs, DMRs (“device master record”) and other technical and production documentation, timely review batch records and related forms to ensure compliant with GDP.
?Provides technical and validation support with regard to equipment IQ/OQ/PQ and process validation activities as need.
?Effective communication and collaboration within department and external interfaces with Facility and Engineering, Technical Operations, Warehouse and Quality etc..
?Timely investigate and report product quality issues and provide technical support as need.
?Maintains safe and healthy work environment by establishing and enforcing organization standards.
?Ability to work well with others.
?Ability to work with cross-site production and development teams.
?Ability to travel domestically and internationally.

This position may suit you best, if building learning organizations is your expertise and you have extensive experience with Top Management Learning and Leadership Development.

?Experience:
-Typically 3-5 years of successful experience in a directly related field (GMP and CFDA regulated environment, IVD experience a plus) and successful demonstration of Key Responsibilities and Knowledge as presented above, project management experience is a plus.
-Knowledge and experience in Quality Management (CAPA, IR, Quality Notifications).
-Knowledge and experience in Staffing, Delegation, Performance Management, Foster Teamwork, Self-Development, Giving Feedback.
-Microsoft Office experience required

?Education:
-BS degree above in Pharmaceutical, Chemistry, Biochemistry, or related field.