Job Description
We are a leading world supplier of integrated processing solutions for customers in the area of pharmaceuticals, food processing, feeds and fine chemicals. Our products and services stand for reliability and quality worldwide. About 3,000 employees work for Glatt at more than 15 companies and offices all over the world. For our site in Ramsey, NJ (USA) we have an immediate opening for a
Scientist II (Drug Product Manufacturing)
Job responsibilities:
Assess and compare emerging formulation and process technologies including Glatt fluid-bed granulation, drying, and Wurster coating platforms to determine how these capabilities can address current client challenges and support future CDMO project opportunities. Provide scientific input to link laboratory and pilot-scale Glatt processing data with client needs, market trends, and areas where our capabilities can offer differentiated technical value. Design and conduct feasibility studies and pilot-scale evaluations for client programs involving advanced drug delivery systems, multiparticulates, or continuous processing concepts using Glatt equipment. This includes optimizing atomization conditions, spray rates, inlet temperatures, and product temperatures to meet project-specific CQAs. Work closely with development team to confirm the technical viability of client-requested processes and collaborate with project teams to translate these findings into development plans tailored to client timelines and regulatory expectations. Perform API solubility studies, forced degradation and physical evaluations of finished dosage forms to directly link laboratory and pilot-scale Glatt processing data to client needs and market expectations. Prepare detailed analytical and scientific reports to clearly communicate experimental outcomes, trends, deviations and next steps, and present both technical and non-technical audiences Glatt’s processing results, scale-up implications, and development recommendations are understood by internal teams, Business Development, and client technical group.
Qualifications and Experience:
Must have Master’s degree in Pharmaceutical Science or Chemical Engineering.
Must have two years of experience working in a pharmaceutical industry with experience in solid oral products and dosage formulation, controlled release products and understanding of fluid bed technology.
Strong experience with cGMP, DEA and regulatory requirements.
Must have proof of legal authority to work in the United States. 40 hours per week, M-F, 9am – 5pm. Salary: $103,085.00 -$120,000.00 per year. Job Requisition #2023XXXXXX.
You have the opportunity to perform an interesting and responsible job in a successful, renowned company.
If this interesting position appeals to you, we look forward to receiving your online application.
Applications that do not reach us personally via the online portal can unfortunately not be considered.
Glatt Air Techniques Inc., Human Resources, 20 Spear Road, Ramsey, NJ 07446, USA www.glatt.com
Scientist II (Drug Product Manufacturing)
Job responsibilities:
Assess and compare emerging formulation and process technologies including Glatt fluid-bed granulation, drying, and Wurster coating platforms to determine how these capabilities can address current client challenges and support future CDMO project opportunities. Provide scientific input to link laboratory and pilot-scale Glatt processing data with client needs, market trends, and areas where our capabilities can offer differentiated technical value. Design and conduct feasibility studies and pilot-scale evaluations for client programs involving advanced drug delivery systems, multiparticulates, or continuous processing concepts using Glatt equipment. This includes optimizing atomization conditions, spray rates, inlet temperatures, and product temperatures to meet project-specific CQAs. Work closely with development team to confirm the technical viability of client-requested processes and collaborate with project teams to translate these findings into development plans tailored to client timelines and regulatory expectations. Perform API solubility studies, forced degradation and physical evaluations of finished dosage forms to directly link laboratory and pilot-scale Glatt processing data to client needs and market expectations. Prepare detailed analytical and scientific reports to clearly communicate experimental outcomes, trends, deviations and next steps, and present both technical and non-technical audiences Glatt’s processing results, scale-up implications, and development recommendations are understood by internal teams, Business Development, and client technical group.
Qualifications and Experience:
Must have Master’s degree in Pharmaceutical Science or Chemical Engineering.
Must have two years of experience working in a pharmaceutical industry with experience in solid oral products and dosage formulation, controlled release products and understanding of fluid bed technology.
Strong experience with cGMP, DEA and regulatory requirements.
Must have proof of legal authority to work in the United States. 40 hours per week, M-F, 9am – 5pm. Salary: $103,085.00 -$120,000.00 per year. Job Requisition #2023XXXXXX.
You have the opportunity to perform an interesting and responsible job in a successful, renowned company.
If this interesting position appeals to you, we look forward to receiving your online application.
Applications that do not reach us personally via the online portal can unfortunately not be considered.
Glatt Air Techniques Inc., Human Resources, 20 Spear Road, Ramsey, NJ 07446, USA www.glatt.com
💡 Quick Summary
Seeking a career-building opportunity? The Scientist II (Drug Product Manufacturing) position is now open for candidates interested in the Health Jobs sector. This role in New York City offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Health Jobs is a plus.
