Our client is currently the leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. They’re looking to hire a Process Improvement Data Specialist to join their team!

JOB DESCRIPTION:

• Responsible for the collection, statistical analysis, and visualization of production data to enhance manufacturing processes, efficiency, and robustness.
• Analyze data from both ongoing and historical manufacturing activities, providing actionable insights and recommendations to the management team.
• Identify areas for improvement in production processes and recommend necessary actions or controls to enhance performance.
• Generate and track Key Performance Indicators (KPIs) to help focus strategic and operational improvements.
• Work as an individual contributor within the production department, coordinating with other teams and sites as necessary.
• Communicate findings effectively to management using data visualizations, reports, and presentations.
• Collaborate with cross-functional teams, ensuring adherence to regulatory requirements and company standards.

QUALIFICATIONS:

• BA/BS in any scientific discipline.
• Minimum of 3 years of experience in a GMP (Good Manufacturing Practice) environment.
• Proficient in statistical analysis applied to pharmaceutical manufacturing.
• Exposure to reporting tools.
• Knowledge of FDA regulations and compliance standards in a manufacturing setting.
• Exceptional written and oral communication skills, with the ability to present complex data clearly.
  This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Please refer the Job description for details