Biochemist II

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The Biochemist II serves a key role within the Standards Manufacturing team at the Siemens Healthineers East Walpole facility. This position involves technical leadership and hands‑on participation in the production of laboratory diagnostic standards and controls within a cGMP‑compliant environment. The primary functions include ensuring adherence to regulatory requirements, providing technical guidance to manufacturing technicians, and acting as a Subject Matter Expert (SME) in cross‑functional projects.

The role reports directly to the Senior Manager of Manufacturing‑Formulation.

• Audit manufacturing documentation, including Manufacturing Batch Records, Bills of Materials, Routings, Process Documents, and Standard Operating Procedures (SOPs), to ensure strict cGMP compliance.
• Provide technical guidance and training to manufacturing technicians, ensuring they are qualified for all manufacturing activities.
• Coordinate and monitor the day‑to‑day work centre assignments in collaboration with the Standards Manufacturing Senior Supervisor.
• Represent the Standards Manufacturing department in cross‑functional team meetings, including design element teams, planning and scheduling, and product troubleshooting projects.
• Identify and initiate continuous improvement activities consistent with the Healthineers Performance System (HPS) framework.
• Provide direct support on the manufacturing floor as needed to ensure production schedules and work centre demands are met.
• May temporarily assume a supervisory role on a limited basis with direct support from the Senior Manufacturing Manager.

• Education:
  
  Bachelor’s degree (BS) in Medical Technology, Biology, Chemistry, Biochemistry, or a related scientific discipline.
• Experience:
  
  Minimum of five (5) years of experience in a similar role within the medical diagnostic or medical device industry.
• Regulatory Knowledge:
  Solid working knowledge of cGMP (Current Good Manufacturing Practices) requirements.
• Skills:
  
  Excellent organizational and time management abilities, high attention to detail, commitment to accuracy, and established critical thinking and problem‑solving skills.

• Prior experience manufacturing commercialised automated immunoassays, ELISA, and/or chemiluminescent products.
• Proficiency with Microsoft Office suite applications.
• Prior knowledge and use of SAP or a similar Material Requirements Planning/Enterprise Resource Planning (MRP/ERP) system.

Base Pay Range For This Position Is
Min $95,770 - Max $143,650

Benefits:
Medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long‑term and short‑term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.

Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and affirmative action employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, colour, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, 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, .

Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that…