QC Manufacturing Supervisor

QC Manufacturing Supervisor
Locations:East Walpole, Massachusetts
Job Family: Manufacturing
English (US)
Job Description
Division: Siemens Healthineers
Business Unit: Laboratory Diagnostics
Requisition Number: 218224
Primary Location: United States-Massachusetts-East Walpole
Assignment Category: Full-time regular
Experience Level: Mid level
Education Required Level: Bachelor's Degree
Travel Required: No
Division Description:
Siemens is a global technology powerhouse that has stood for engineering excellence, innovation, quality, reliability and internationality for more than 165 years. As a global technology company, Siemens is rigorously leveraging the advantages that this setup provides. To tap business opportunities in both new and established markets, the Company is organized in nine Divisions: Power and Gas, Wind Power and Renewables, Energy Management, Building Technologies, Mobility, Digital Factory, Process Industries and Drives, Healthineers and Financial Services.
With 45,000 employees Siemens Healthineers is one of the world?s largest suppliers of technology to the healthcare industry and a leader in medical imaging, laboratory diagnostics and healthcare IT. All supported by a comprehensive portfolio of clinical consulting, training, and services available across the globe and tailored to customers? needs. So that more people can have a life that is longer, richer, and more filled with happiness.
For more information, please visit: http://www.usa.siemens.com/healthineers
Job Description:
Supervisor, Immunoassay Quality Control
This position is responsible for supporting all aspects of the Immunoassay Quality Control Lab Testing Group. This includes scheduling and prioritizing commercial production testing as well as Design Change QC (DCQC) testing.
Responsibilities include:
- Provide guidance and technical support to personnel
- Direct supervision and management of personnel
- Managing and providing oversight of the QC Testing Lab
- Collaborating with QC Witness, QC Approval and DCQC Group
- Creation of job requisitions, interviewing, and hiring
- Quality Notification input/review
- Provide recommendations for document redlines
- Initiate and drive complex and impactful process, environment and/or employee improvements
- Ensure testing execution and testing data is compliant
Bachelor's degree - Life Science discipline
- Excellent verbal and written communication skills
- Excellent organizational and time management skills
- Ability to work individually and in a team setting
-BS with 1-3 years
- Previous supervisory experience required.
- Experience working in a cGMP biotechnology environment a plus
Equal Employment Opportunity Statement
Siemens is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, protected veteran or military status, and other categories protected by federal, state or local law.
EEO is the Law
Applicants and employees are protected under Federal law from discrimination. To learn more, Click here at https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm .
Pay Transparency Non-Discrimination Provision
Siemens follows Executive Order 11246, including the Pay Transparency Nondiscrimination Provision. To learn more, Click here at https://www.dol.gov/ofccp/pdf/pay-transp_formattedESQA508c.pdf .

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