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The Principal Automation Engineer will design, verify, and validate DeltaV automation systems and support GMP manufacturing operations. Responsibilities include system administration, collaboration with quality and engineering teams, and mentoring others in safety and engineering principles.

The position involves developing predictive models for ADMET and PK/PD, enabling biotech partners through clear model outputs, and mentoring junior scientists.

The Advisor in Computational Statistics collaborates on statistical analysis plans, conducts data analysis using SAS and R, communicates results, ensures regulatory compliance, and maintains proficiency in statistical methods.

Lead quality assurance for GMP operational readiness at a site, ensuring compliance, inspection readiness, and effective risk management during the startup phase and beyond.

The Supply Chain Associate will manage supply chain processes, ensuring reliable delivery of medicines through oversight of contract manufacturing and inventory management.

The Quality Intern will assist in managing product complaints, perform translations, sample requests, cargo arrangements, and support the Quality team's compliance with policies and procedures.

Provide legal counsel and regulatory expertise for clinical development. Involve modernization through AI and support clinical trial operations while ensuring compliance with legal standards.