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Process Development Scientist - Job Opportunity at PRPDG

Juncos, US
Full-time
Senior
Posted: May 12, 2025
On-site
USD 85,000 - 120,000 per year based on Puerto Rico market conditions and senior-level technical requirements

Benefits

Implied: Professional development opportunities in advanced manufacturing
Implied: Work with cutting-edge vision system technologies
Implied: Collaborative research environment

Key Responsibilities

Lead experimental strategy design and execution for process optimization and validation
Conduct complex data analysis and impact assessment for manufacturing processes
Develop and implement testing protocols for vision system technologies
Execute equipment characterization and validation procedures
Generate technical documentation and risk assessment reports

Requirements

Education

Doctorate degree or Master degree with 5 years experience or Bachelor degree with 6 years experience

Experience

5-6 years minimum depending on education level

Required Skills

Vision system technologies Inspection/packaging concepts Process development Equipment characterization Testing strategy development Protocol design Technical report writing Validation execution Risk assessment QRAES knowledge
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Sauge AI Market Intelligence

Industry Trends

The pharmaceutical and medical device manufacturing sector is experiencing rapid automation integration, particularly in vision system technologies for quality control and process validation. Increasing regulatory scrutiny is driving demand for expertise in risk assessment and validation protocols, especially in FDA-regulated environments. The convergence of traditional process development with digital transformation is creating hybrid roles that require both scientific expertise and technology understanding.

Role Significance

Typically part of a 5-10 person process development team, collaborating with validation, quality, and manufacturing departments
Senior technical position with significant influence on process development and validation strategies, typically reporting to Technical Operations or R&D leadership

Key Projects

Implementation of new manufacturing process validation protocols Vision system technology integration and optimization Risk assessment and mitigation strategy development Equipment qualification and characterization programs

Success Factors

Deep understanding of GMP and FDA validation requirements Ability to bridge technical expertise with practical implementation Strong documentation and technical writing capabilities Experience with risk-based validation approaches Effective cross-functional collaboration skills

Market Demand

High demand driven by manufacturing automation trends and increasing complexity of regulatory compliance requirements in pharmaceutical/medical device manufacturing

Important Skills

Critical Skills

Vision system technology expertise is crucial as manufacturing moves toward automated inspection and control Validation protocol development and execution capabilities are essential for regulatory compliance Risk assessment expertise is fundamental for modern GMP manufacturing environments

Beneficial Skills

Project management skills for coordinating complex validation programs Statistical analysis for process optimization Quality system regulation knowledge Change control management expertise

Unique Aspects

Combination of scientific expertise with automation technology focus
Strong emphasis on risk assessment and validation methodologies
Integration of vision system technologies with traditional process development

Career Growth

2-4 years in role before advancement, depending on project success and organizational growth

Potential Next Roles

Senior Process Development Manager Validation Technical Lead Manufacturing Technology Director Quality Systems Manager

Company Overview

PRPDG

PRPDG appears to be involved in regulated manufacturing, likely in the pharmaceutical or medical device sector, with significant investment in automation and quality control systems

Regional player in the manufacturing sector with emphasis on technical excellence and regulatory compliance
Significant presence in Puerto Rico's pharmaceutical/medical device manufacturing hub
Technical excellence-focused environment with emphasis on precision, documentation, and regulatory compliance
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