Honeywell International Inc.
Senior QA Scientist
Honeywell International Inc., Buffalo, New York, United States, 14266
Innovate high-purity, high-performance chemicals and materials
Be part of a team that applies its expertise and knowledge to technical projects, finding innovative, cost-effective means to improve research, techniques, procedures, and products and technologies. You will facilitate design, development, and testing to meet project objectives faster and more efficiently and you develop and commercialize products & technologies.Key Responsibilities
InnovationCost estimationPrototypingProduct AssuranceProject managementCustomer InteractionCustomer communicationResearch and DevelopmentRisk ManagementDesign analysisYOU MUST HAVEBachelor’s degree in Chemistry, Chemical Engineering, or Quality Assurance management; advanced degree is preferred.5+ years of experience managing cGMP Quality Assurance related to cGMP production of drugs or drug excipients.2+ years experience of conducting and managing root cause analysis, risk assessment, CAPA, batch review and document control.2+ years of experience with practical application of FDA 21 CFR Part 211 and 21 CFR Part 11 in a chemical manufacturing plant.2+ years of experience in conducting and hosting cGMP compliance audits.WE VALUEExperience in a fast-paced environment.2+ years of experience with common chemical process unit operations is preferred.Additional Information
JOB ID:
req459119Category:
EngineeringRelocation Tier:Security Clearance:Aviation Authority (FAA for US):Band:
03Referral Bonus:
1500Requisition Type:
Pre-sourcing RequisitionUS Citizenship:
Due to US export control laws, must be a US citizen, permanent resident or have protected status.FLSA CODE:
ExemptHoneywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.
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Be part of a team that applies its expertise and knowledge to technical projects, finding innovative, cost-effective means to improve research, techniques, procedures, and products and technologies. You will facilitate design, development, and testing to meet project objectives faster and more efficiently and you develop and commercialize products & technologies.Key Responsibilities
InnovationCost estimationPrototypingProduct AssuranceProject managementCustomer InteractionCustomer communicationResearch and DevelopmentRisk ManagementDesign analysisYOU MUST HAVEBachelor’s degree in Chemistry, Chemical Engineering, or Quality Assurance management; advanced degree is preferred.5+ years of experience managing cGMP Quality Assurance related to cGMP production of drugs or drug excipients.2+ years experience of conducting and managing root cause analysis, risk assessment, CAPA, batch review and document control.2+ years of experience with practical application of FDA 21 CFR Part 211 and 21 CFR Part 11 in a chemical manufacturing plant.2+ years of experience in conducting and hosting cGMP compliance audits.WE VALUEExperience in a fast-paced environment.2+ years of experience with common chemical process unit operations is preferred.Additional Information
JOB ID:
req459119Category:
EngineeringRelocation Tier:Security Clearance:Aviation Authority (FAA for US):Band:
03Referral Bonus:
1500Requisition Type:
Pre-sourcing RequisitionUS Citizenship:
Due to US export control laws, must be a US citizen, permanent resident or have protected status.FLSA CODE:
ExemptHoneywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.
#J-18808-Ljbffr