Lensa

Process Improvement Data Specialist

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Process Improvement Data Specialist in Vista, CA, offering $40-45/hr for a 4-6 month contract. Requires a BA/BS, 3+ years in GMP, proficiency in statistical analysis, and knowledge of FDA regulations.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
360
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🗓️ - Date
February 22, 2026
🕒 - Duration
3 to 6 months
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🏝️ - Location
On-site
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📄 - Contract
Unknown
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🔒 - Security
Unknown
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📍 - Location detailed
Vista, CA
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🧠 - Skills detailed
#Compliance #Visualization
Role description
Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Astrix Technology. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Process Improvement Data Specialist Manufacturing Vista, California, US • Added - 21/01/2026 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! Title: Process Improvement Data Specialist Location: Vista, CA (Fully onsite) Pay: $40-45/hr Contract: 4-6 months+ benefits (Likely to extended) 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! INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. If you have questions about this posting, please contact support@lensa.com