Process Improvement Data Specialist

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Process Improvement Data Specialist in San Diego County, California, with a 6-month contract at $30-35/hr. Requires a BA/BS, 3 years in a GMP environment, statistical analysis skills, and knowledge of FDA regulations.
🌎 - Country
United States
πŸ’± - Currency
$ USD
-
πŸ’° - Day rate
280
-
πŸ—“οΈ - Date discovered
September 4, 2025
πŸ•’ - Project duration
More than 6 months
-
🏝️ - Location type
On-site
-
πŸ“„ - Contract type
Unknown
-
πŸ”’ - Security clearance
Unknown
-
πŸ“ - Location detailed
Vista, CA
-
🧠 - Skills detailed
#Compliance #Visualization
Role description
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! Contract (6 Months) Pay: $30-35/hr San Diego County, California Job Description β€’ Responsible for the collection, statistical analysis, and visualization of production data to enhance manufacturing processes, efficiency, and robustness. β€’ Analyze data from both ongoing and historical manufacturing activities, providing actionable insights and recommendations to the management team. β€’ Identify areas for improvement in production processes and recommend necessary actions or controls to enhance performance. β€’ Generate and track Key Performance Indicators (KPIs) to help focus strategic and operational improvements. β€’ Work as an individual contributor within the production department, coordinating with other teams and sites as necessary. β€’ Communicate findings effectively to management using data visualizations, reports, and presentations. β€’ Collaborate with cross-functional teams, ensuring adherence to regulatory requirements and company standards. Qualifications β€’ BA/BS in any scientific discipline. β€’ Minimum of 3 years of experience in a GMP (Good Manufacturing Practice) environment. β€’ Proficient in statistical analysis applied to pharmaceutical manufacturing. β€’ Exposure to reporting tools. β€’ Knowledge of FDA regulations and compliance standards in a manufacturing setting. β€’ 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! INDBH