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High Point, NC
Source: Verista, Inc. careers · View original posting
From Verista, Inc.'s posting. “We” and “our” refer to the employer.
Description
Verista’s
500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
We constantly acquire new skills and learn from our experiences to enhance our collective expertise
Serve as a technical SME for API micronization and particle-size reduction processes.
Develop, optimize, and troubleshoot micronization and milling processes using equipment such as jet mills, Fitz Mills, and cryogenic milling systems.
Lead or support process development, characterization, scale-up, and technology transfer activities for R&D-stage API programs.
Evaluate and characterize Particle Size Distribution (PSD) and establish appropriate particle-size targets, ranges, and control strategies.
Assess the relationship between milling parameters, particle characteristics, material properties, and overall product/process performance.
Identify and define Critical Process Parameters (CPPs) and relevant Critical Quality Attributes (CQAs) associated with micronization.
Design and execute studies to improve process understanding, robustness, reproducibility, and scalability.
Support development of processes suitable for future GMP manufacturing, process validation, PPQ, and commercialization.
Partner cross-functionally with R&D, Process Development, Manufacturing, Quality, Analytical, Validation, and other technical teams.
Author and review technical documentation, development reports, protocols, risk assessments, and technology-transfer documentation.
Troubleshoot milling and particle-size issues and provide technically sound recommendations for process improvement.
Ensure development activities appropriately consider future regulatory, GMP, validation, and commercial manufacturing requirements.
For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
National (US) Range
$95,865 — $181,634 USD
*Verista is an equal opportunity employer.
LAYIQ is an independent job-discovery service. This listing does not imply a partnership with or endorsement by the employer. Review the original posting for current details and availability.
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