Process Engineer
24 hours ago
Wharton, New Jersey, United States
DMI Solutions Wharton
Full-time
$73,000 - $76,000 Contract
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Purpose of Position:
This position is primarily responsible for the development of pilot and full-scale manufacturing processes for skincare, personal care, and color cosmetic products.
Essential Functions:
• Develops and revises Master Batch Record documentation related to internal and external formula transfers in collaboration with R&D and customers
• Develops and maintains a liaison with R&D, Quality Control, Manufacturing and other departments to successfully manufacture pilots, production batches, troubleshoot in-process batches, and implement process improvements
• Records observations and provides processing recommendations on new product scale-up activities, pilots, and first production batches in Manufacturing
• Independently conduct benchwork for the troubleshooting of cosmetic formulations (including hot pours) and provide processing recommendations
• Assist Validation Specialist in conducting validation swab testing as required
• Evaluates and recommends new processing equipment & systems for bulk manufacturing to ensure continued sophistication and improvement in the manufacturing department
• Adheres to GMP guidelines in the maintenance of documents, manufacturing and change control procedures Qualifications
• Bachelor’s degree in a scientific discipline (Engineering, Biology, Chemistry, etc.)
• 3+ year experience in process engineering with personal care products (preferred)
• Proficient in Microsoft Excel and Word
• Ability to monitor critical/urgent manufacturing activities on-site beyond typical shift hours as needed with team support
• Must be able to think critically and analytically (“Think outside the box”) to resolve issues and make improvements
• Bilingual in English/Spanish and Color-matching experience an asset. Applicants must be legally authorized to work in the United States. At this time, we are unable to provide employment-based visa sponsorship or assume sponsorship from another employer. Compensation details: 73000-76000 Yearly Salary
• Develops and revises Master Batch Record documentation related to internal and external formula transfers in collaboration with R&D and customers
• Develops and maintains a liaison with R&D, Quality Control, Manufacturing and other departments to successfully manufacture pilots, production batches, troubleshoot in-process batches, and implement process improvements
• Records observations and provides processing recommendations on new product scale-up activities, pilots, and first production batches in Manufacturing
• Independently conduct benchwork for the troubleshooting of cosmetic formulations (including hot pours) and provide processing recommendations
• Assist Validation Specialist in conducting validation swab testing as required
• Evaluates and recommends new processing equipment & systems for bulk manufacturing to ensure continued sophistication and improvement in the manufacturing department
• Adheres to GMP guidelines in the maintenance of documents, manufacturing and change control procedures Qualifications
• Bachelor’s degree in a scientific discipline (Engineering, Biology, Chemistry, etc.)
• 3+ year experience in process engineering with personal care products (preferred)
• Proficient in Microsoft Excel and Word
• Ability to monitor critical/urgent manufacturing activities on-site beyond typical shift hours as needed with team support
• Must be able to think critically and analytically (“Think outside the box”) to resolve issues and make improvements
• Bilingual in English/Spanish and Color-matching experience an asset. Applicants must be legally authorized to work in the United States. At this time, we are unable to provide employment-based visa sponsorship or assume sponsorship from another employer. Compensation details: 73000-76000 Yearly Salary