TS/MS Scientist – Dry-EM: Spray Dry & Tech Transfer

Pinnaql, Inc.; Manatí (PR); On-site; USD 90,000 - 130,000; Full time

Job summary

Validation & Engineering Group, Inc. (V&EG), a Pinnaql company, seeks an experienced TS/MS Scientist - Dry EM to provide technical leadership in spray dry and solid dosage manufacturing for external partners.

The role focuses on process validation, technology transfer, deviations, CAPA, and regulatory compliance across cGMPs. Applicants should have a bachelor's degree in a scientific discipline and 5+ years of hands-on experience, with strong writing skills and ability to collaborate across

Qualifications

• Bachelor's degree in Chemistry, Pharmacy, or Engineering.
• 5+ years hands-on experience with spray dry and solid dosage manufacturing.
• Working knowledge of regulatory expectations (cGMP) and global guidelines.
• Experience supporting external manufacturing (CMOs) and technology transfer.

Responsibilities

• Provide technical oversight for spray dry and solid dosage processes.
• Resolve technical issues related to control strategy and manufacturing.
• Author deviations and change controls with strong technical writing.
• Support CAPA investigations and closure within timelines.
• Manage relationships with external partners and cross-functional teams.
• Ensure manufacturing processes are compliant, in control, and validated.
• Support tech transfer and validation with external partners.

Skills

Spray Dry Dispersion (SDD)

Solid Dosage Manufacturing

Packaging Operations

Regulatory Knowledge (cGMP)

Data Management

Cross-functional Collaboration

Project Management

SAP Experience

Statistical Analysis

FDA-regulated Manufacturing

Bilingual English/Spanish

Education

Bachelor's degree in Chemistry, Pharmacy, or Engineering

Tools

SAP

Job description

Validation & Engineering Group, Inc. (V&EG), a Pinnaql company, seeks an experienced TS/MS Scientist - Dry EM to provide technical leadership in spray dry and solid dosage manufacturing for external partners.

The role focuses on process validation, technology transfer, deviations, CAPA, and regulatory compliance across cGMPs. Applicants should have a bachelor's degree in a scientific discipline and 5+ years of hands-on experience, with strong writing skills and ability to collaborate across