Siemens Biochemist 1 in East Walpole, Massachusetts
Locations:East Walpole, Massachusetts
Job Family: Research & Development
Division: Siemens Healthineers
Business Unit: Laboratory Diagnostics
Requisition Number: 210993
Primary Location: United States-Massachusetts-East Walpole
Assignment Category: Full-time regular
Experience Level: Mid level
Education Required Level: Bachelor's Degree
Travel Required: 20%
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
This Biochemist 1 position will be responsible for applying scientific principles to accomplish a wide variety of technical assignments for the Immunoassay (IA) Quality Control (QC) group, relating to the China Manufacturing Project. This includes assisting the QC Senior Supervisor and team with the development and implementation of the Immunoassay QC department for the China Manufacturing Facility, which includes Incoming Inspection, Microbiology & Environmental Monitoring, and In-Process & Final QC Release. This position is based in Walpole, MA and report to the QC Senior Supervisor, also based in Walpole.
Collaborate with cross-functional groups (domestic and international) to support project needs
Participate in the training of China-based personnel during visits to both the Walpole site as well as potentially the China manufacturing facility
Contribute to the review, creation, and revision of Quality Control documentation (Material Specifications, Certificate of Analysis’, etc… to support project needs
Initiate and support discussions and actions with internal and external key work groups in support of transferring processes, SOPs, etc… to the China Manufacturing facility
Perform QC testing and accurately assess testing data to ensure product specifications are met and DHR is compiled in a compliant manner, according to current c-GMP and site SOP’s
Problem solving – has a working knowledge of available tools related to job function; incorporate the different databases, applications, personal knowledge, and individual experiences to efficiently support project needs
Help to reach department goals and objectives through collaboration and influence
Initiate and drive process, and/or environment, and/or employee improvements
Ability to travel domestically and internationally
May be required to stay late and/or work off-shift hours on any given day
Required Knowledge/Skills, Education, and Experience
Bachelor’s Degree (or equivalent degree) with a discipline in Biology, Chemistry, Biochemistry, Biotechnology; Microbiology, Molecular Biology or Medical Technology is required
At least 3 years’ experience working in a similar role in the medical diagnostic/medical device, FDA-regulated industry
Excellent verbal and written communication skills
Excellent organization and time management skills
High attention to detail and commitment to accuracy
Preferred Knowledge/Skills, Education, and Experience
Verbal/written proficiency in Mandarin is a plus
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
Must be able to work collaboratively with other project team members
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.
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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 .