Senior Tech Support & Process Lead, Vaccine Manufacturing

Jobs2Web

Athens (GA)

On-site

USD 120,000 - 150,000

Full time

46 hours ago
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Job summary

Boehringer Ingelheim is seeking a Principal Specialist to provide technical support and ongoing process monitoring for vaccine manufacturing. You will interact with operations teams, maintain technical data, and lead troubleshooting efforts within a heavily regulated setting to ensure product quality and compliance.

Ideal candidates have a strong background in biology with extensive experience in regulated biopharmaceutical processes, data analysis, and cross-functional collaboration between IO,

Qualifications

  • Bachelor of Science in Biology or related field is required.
  • 5+ years of industry experience in a regulated environment is required.
  • Advanced degree (MS/PhD) preferred with 10+ years of industry experience.
  • Experience with DM AIC, root cause analysis, and process monitoring is required.

Responsibilities

  • Escalate production flow disturbances and participate in root cause identification.
  • Maintain technical data and support documentation.
  • Lead technical team for process monitoring.
  • Develop troubleshooting protocols for production outlines.
  • Collaborate with QA, RA for Change Control Requests and Product Quality Reviews.

Skills

Root cause analysis
DMAIC methodology
Statistical analysis
Process monitoring
Technical writing
Regulatory interface
Cross-functional collaboration
Communication with operations

Education

Bachelor of Science in Biology or related field
Master of Science in Biology or related field
Doctorate in Biology or related field

Job description

Boehringer Ingelheim is seeking a Principal Specialist to provide technical support and ongoing process monitoring for vaccine manufacturing. You will interact with operations teams, maintain technical data, and lead troubleshooting efforts within a heavily regulated setting to ensure product quality and compliance.

Ideal candidates have a strong background in biology with extensive experience in regulated biopharmaceutical processes, data analysis, and cross-functional collaboration between IO,

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