Pharma Project Manager: Tech Transfer & Process Validation

Loxo; Puerto Rico; On-site; USD 90,000 - 120,000; Full time

Job summary

Loxo is seeking a Project Manager with pharmaceutical industry experience, specializing in technology transfer and process validation for solid dosage forms (tablets and capsules). You will coordinate cross-functional activities, ensure regulatory alignment, timelines, and project objectives, while driving Lean and Right First Time initiatives.

The role requires onsite work in Puerto Rico East/South, immediate availability, and Puerto Rico residency.

Qualifications

• Bachelor’s degree in Science, such as Pharmacy or Engineering.
• 5-7 years of pharmaceutical industry experience, with technology transfer and process validation.
• Immediate availability and Puerto Rico residency.
• Onsite work in East/South Puerto Rico.

Responsibilities

• Coordinate project development strategies to align with site strategy and product sourcing.
• Lead impact and feasibility assessments for product changes.
• Coordinate and track project requirements across relevant functions.
• Identify resources and form project teams.
• Negotiate and establish implementation timelines.
• Ensure checklists are current for each project lifecycle.
• Develop timelines for new products and launches.
• Coordinate product launch activities and tech transfers.
• Identify issues impacting launches and transfers and implement contingencies.
• Promote Lean and Right First Time initiatives.
• Drive process improvement in manufacturing and project activities.
• Ensure harmonized use of local and global systems.
• Support budget preparation and assumptions for new products/transfers.
• Ensure regulatory compliance for project activities.

Education

Bachelor's degree in Science

Pharmacy or Engineering

5-7 years pharmaceutical industry experience

Technology Transfer

Process validation

Lean

Right First Time (RFT)

Job description

Loxo is seeking a Project Manager with pharmaceutical industry experience, specializing in technology transfer and process validation for solid dosage forms (tablets and capsules). You will coordinate cross-functional activities, ensure regulatory alignment, timelines, and project objectives, while driving Lean and Right First Time initiatives.

The role requires onsite work in Puerto Rico East/South, immediate availability, and Puerto Rico residency.