Scientist, II PDS&T (24 month Contract)

This is an exciting opportunity to work in a collaborative, science-driven environment where you'll have ownership of projects, solve complex technical challenges, and contribute to delivering high-quality medicines that make a difference to patients worldwide.
What You'll Do
As part of our team, you will:
Design, plan, and execute laboratory studies to support formulation development, process optimization, scale-up activities, and technology transfers.
Perform and support parenteral drug product activities including compounding, filtration, and filling operations.
Analyze and interpret scientific data, identify trends, troubleshoot issues, and make data-driven recommendations.
Author and review technical documents, protocols, reports, procedures, and batch records.
Support laboratory start-up activities, equipment qualification, and facility readiness in collaboration with engineering, quality, and manufacturing teams.
Work with internal stakeholders and external vendors to evaluate and improve equipment, systems, and technologies.
Lead or contribute to investigations, risk assessments, change controls, and problem-solving initiatives.
Ensure compliance with GMP, quality, data integrity, and safety requirements.
Drive continuous improvement, digitalization, and knowledge-sharing initiatives across the team.
Education
You will hold a Bachelor's, Master's, or PhD in:
Pharmaceutical Science
Biotechnology
Chemical or Process Engineering
Drug Discovery & Development
Or another relevant scientific or engineering discipline
Experience
You will have experience in a pharmaceutical, biotechnology, medical device, technical operations, manufacturing, or regulated laboratory environment.
Level will be determined based on experience:
Bachelor's Degree: typically 5-7+ years' relevant experience
Master's Degree: typically 3-5+ years' relevant experience
PhD: typically 1-2+ years' relevant experience
You'll also bring:
Experience planning and executing scientific experiments independently.
Strong analytical and problem-solving skills with the ability to interpret complex data.
Knowledge of GMP/GxP requirements, quality systems, validation concepts, and data integrity principles.
Experience with sterile manufacturing, aseptic processing, filtration, formulation development, lyophilization, or related parenteral technologies would be an advantage.
A proven ability to collaborate effectively within cross-functional project teams.

Employment type
Full-time

Work arrangement
No