Solid Dose Process Engineer

Location: Phoenix, Arizona Experience Level: Entry-Level to Mid-Level Industry: Solid Dose Agglomeration/Granulation Manufacturing | Dietary Supplements | GMP Manufacturing About Us Marlyn Nutraceuticals is a leading manufacturer of premium dietary supplements, combining scientific innovation with sustainable manufacturing practices. Our FDA-registered, GMP-certified Arizona facility features state-of-the-art technology for solid dose manufacturing. We provide an ideal environment for engineers to transform their technical knowledge into practical expertise while working with advanced manufacturing systems including: Continuous dry granulation and roller compaction systems High-shear mixing and agglomeration technology Advanced fluid bed processing equipment Solid dose direct compression process methods The Opportunity Join our Product Development team as a Process Engineer and help drive innovation in pharmaceutical/nutraceutical solid dose manufacturing processes. This role offers exceptional growth potential for engineers passionate about advancing solid dose manufacturing technology. You'll collaborate with our expert team while: Optimizing powder characteristics through advanced solid dose material processing techniques Developing innovative solvent-free manufacturing methods Implementing continuous manufacturing processes Managing scale-up from R&D to commercial production Applying Quality by Design (QbD) principles Core Responsibilities Lead particle engineering projects focused on improving powder flow and compression characteristics Design and optimize dry granulation and direct compression processes Develop and validate analytical methods for material characterization Conduct DoE (Design of Experiments) studies for process optimization Maintain compliance with cGMP requirements and FDA regulations Support technology transfer activities from R&D to trial & commercial manufacturing Participate in process validation and qualification activities Required Qualifications - BS/MS in Chemical Engineering, Materials Processing, Solid Dose chemistry, or Material science - Understanding of: Powder technology and solid dose material/particle Solid-state characterization methods Process engineering fundamentals Basic statistical analysis - Strong analytical and problem-solving skills - Excellent documentation and communication abilities - Ability to work in a GMP-regulated environment Preferred Qualifications - Experience with analytical techniques: Particle size analysis Powder rheology testing Thermal analysis (DSC/TGA) Surface area analysis - Knowledge of: Design of Experiments (DoE) Statistical process control GMP requirements - Previous internship or laboratory experience - Familiarity with solid dose RD bench processing and physical testing techniques Benefits & Growth Opportunities - Comprehensive training program including: GMP training Solid dose manufacturing courses RD process and testing Equipment operation training - Career advancement pathway - Competitive compensation package: Competitive salary Annual performance bonus - Full benefits including: Medical, dental, and vision coverage 401(k) with 25% company match Paid time off Life and disability insurance Location & Work Environment Modern, climate-controlled GMP manufacturing facility State-of-the-art R&D laboratory Collaborative team environment To apply, please submit your resume and cover letter detailing your interest in solid dosage manufacturing and process engineering. ***************** Marlyn Nutraceuticals is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.​​ #Process Engineer, #Pharmaceutical Manufacturing, #GMP Manufacturing, #Chemical Engineer, #Material Science Engineer, #Solid Dose Manufacturing, #Powder Technology, #Partical Engineering, #Process Development, #Granulation Technology, #Roller Compaction, #Direct Compression, #Direct Compression, #cGMP, #FDA Regulated, #Quality by Design, #Process Validation, #Technology Transfer, #DoE, #Process Optimization, #Material Characterization, #Phoenix, Arizona, #Greater Phoenix Area, #Southwest Manufacturing, #Arizona Manufacturing