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

• Innovation
• Cost estimation
• Prototyping
• Product Assurance
• Project management
• Customer Interaction
• Customer communication
• Research and Development
• Risk Management
• Design analysis

YOU MUST HAVE

• Bachelor'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 VALUE

• Experience in a fast-paced environment

• 2+ years of experience with common chemical process unit operations is preferred

Additional Information

• JOB ID: req459119
• Category: Engineering
• Relocation Tier:
• Security Clearance:
• Aviation Authority (FAA for US):
• Band: 03
• Referral Bonus: 1500
• Requisition Type: Pre-sourcing Requisition
• US Citizenship: Due to US export control laws, must be a US citizen, permanent resident or have protected status.
• FLSA Statement:
• FLSA CODE: Exempt

Honeywell 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.