Cosmetics Bulk Process Engineer – Scale-Up & DOE

Intercos America; Congers (NY); On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Health Insurance

401(k) Plan with company matching

Life Insurance

Paid Time Off

Paid holidays

Professional Development

Team-building events

Employee Assistance Programs

Job summary

Intercos Group in Congers, NY is seeking a Bulk Engineer to drive the scale-up of cosmetic formulations from concept to manufacturing. The role requires translating development work into production-ready processes and leading DOE studies to solve processing challenges.

Success requires strong communication across R&D, Manufacturing, and Quality, with a proactive approach to investigate out-of-spec outcomes and implement CAPAs in a cGMP environment.

Qualifications

• B.S. in Chemistry, Chemical/Industrial Engineering, or related degree.
• Minimum four (4) years in a science-related industry, preferably cosmetic & personal care in a cGMP manufacturing environment.
• Strong understanding of chemical processing concepts including heat transfer, mass flow, and instrumental & statistical analysis.
• Exceptional communication skills with an ability to convey data and timelines with cross-functional teams.

Responsibilities

• Scale-up development, planning and execution of industrial-scale formulations and filling trials for smooth transition to manufacturing.
• Create and apply DOE to solve processing challenges.
• Operate in a cGMP environment with knowledge of relevant regulations and standards.
• Investigate manufacturing non-conformances and implement corrective/preventive actions.

Education

B.S. in Chemistry, Chemical/Industrial Engineering, or related degree

Tools

MS Office

Job description

Intercos Group in Congers, NY is seeking a Bulk Engineer to drive the scale-up of cosmetic formulations from concept to manufacturing. The role requires translating development work into production-ready processes and leading DOE studies to solve processing challenges.

Success requires strong communication across R&D, Manufacturing, and Quality, with a proactive approach to investigate out-of-spec outcomes and implement CAPAs in a cGMP environment.