Sr Data Scientist
QRC Group, Inc Juncos, Puerto Rico
Staffing and Recruiting · 51-200 employees
About the role
The Senior Data Scientist will support AI-enabled optimization, resource planning, and validation initiatives within the Drug Product department. Responsibilities include collecting and analyzing operational data, developing digital tools, and ensuring compliance with GMP documentation standards.
What they look for
Requirements
Candidates must possess a degree in a technical field such as data science, engineering, or statistics, with at least 2 to 8 years of relevant experience depending on the degree level. Proficiency in data analysis tools, statistical methods, and bilingual communication in Spanish and English is required.
Benefits
Full description
Company Description
QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!
Job Description
We are seeking Sr Data Scientist, with knowledge of technical, analytical, and operational skills to support AI-enabled optimization, resource planning, and validation-related initiatives within Drug Product.
Experience or demonstrated capability in the following areas:
- Data analytics and visualization.
- Ability to collect, organize, clean, analyze, and interpret complex operational or manufacturing data. Experience with tools such as Excel, Power BI, Smart- sheet, JMP, Minitab, or similar platforms would be highly valuable.
- Programming, automation, and AI-enabled tools.
- Foundational programming or automation experience, including exposure to Python, Codex, AI-assisted coding tools, Power Automate, scripting, database structure, or digital workflow development. The candidate does not need to be an expert programmer but should be comfortable learning and applying digital tools to solve business problems.
- Statistical and process evaluation mindset.
- Understanding of basic statistics, process variability, trending, capacity evaluation, data comparison, and performance monitoring. This would support both workload forecasting and characterization/validation data evaluation.
- Validation and/or GMP documentation experience.
- Knowledge of GMP expectations, validation lifecycle activities, protocol/report development, documentation practices, data integrity, discrepancy follow-up, and compliance-driven execution.
- Strong communication and stakeholder engagement.
- Ability to work with cross-functional teams, gather user requirements, translate business needs into tool requirements, and communicate findings clearly to management and technical stakeholders.
- Be available to support non-standard shift when activities are required.
Qualifications
- Doctorate or Masters + 2 years of data science, business, statistics, data mining, applied mathematics, business analytics, engineering, computer science or related field experience
Bachelors + 4 years of data science, business, statistics, data mining, applied mathematics, business analytics, engineering, computer science or related field experience
Associates + 8 years of data science, business, statistics, data mining, applied mathematics, business analytics, engineering, computer science or related field experience (Industrial Engineering, Systems Engineering, Computer Science, Chemical Engineering, Biomedical Engineering, Biotechnology, Manufacturing Engineering, or a related technical discipline)
- Bilingual (Spanish/English) (Speak/Write)
- Technical Writing
Additional Information
Benefits
What We Offer
- Opportunities for learning, development, and professional growth.
- A collaborative and supportive work environment.
- The opportunity to work with industry-leading clients on impactful projects.
Your information will be kept confidential according to EEO guidelines.
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