Lead bioanalytical and pharmacokinetic studies, manage CROs, mentor scientists, and ensure compliance with regulatory standards in drug development.

The Senior Director, Legal Counsel will manage complex contracts, provide legal advice, lead cross-functional teams, and manage outside counsel in the biotechnology sector.

The CMC Documentation Specialist will manage and coordinate CMC documentation, ensuring compliance with regulatory guidelines and supporting cross-functional teams in documentation efforts.

The role involves analyzing genomic datasets, identifying therapeutic targets for cardiovascular diseases, and collaborating with cross-functional teams to translate findings into clinical applications.

Responsible for QA oversight of QC activities, ensuring compliance with cGMP and regulatory standards, and reviewing stability data and protocols.

The Senior Manager of Accounting will lead the accounting team, manage financial close processes, provide financial analysis, and ensure compliance with accounting standards.

The Associate Director, CMC Analytical will oversee analytical development, manage quality records, support regulatory filings, and provide technical leadership for drug substances and products.

The Associate Director of Quality Compliance will optimize quality processes, lead supplier quality oversight, ensure GMP compliance, and support regulatory inspections and quality risk management.