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The EHS Analyst ensures EHS compliance by assessing risks, conducting audits, and collaborating with various departments on environmental, health, and safety initiatives.

The Planning Manager oversees supply chain efficiency, leads production planning, and drives continuous improvement initiatives while aligning with organizational goals.

The Quality Control Senior Associate Scientist I executes testing for raw materials and drug products, maintaining compliance and quality documentation, and training others.

Oversee Quality Assurance for GMP cell therapy manufacturing, ensuring compliance, batch record review, deviations management, and supporting cross-functional teams.

Lead HR strategy for the site, develop talent pipelines, support leadership in performance management and employee relations, ensuring compliance and engagement.

The Logistics Associate will manage the movement of materials, ensure compliance with policies, operate shipping systems, and maintain inventory accuracy while supporting warehouse operations and documentation.

Lead formulation and process development for pharmaceutical projects, ensuring quality and timely operations, managing documentation and logistics, and troubleshooting scale-up issues.

The Procurement Manager will lead indirect and capital procurement, negotiating contracts, managing supplier performance, and implementing savings strategies to optimize costs.

The Project Manager leads CDMO client projects throughout the product lifecycle, ensuring customer satisfaction and compliance with quality standards while managing relationships and project timelines.

The role focuses on ensuring the compliance and effectiveness of Supplier and Material Quality Assurance programs, conducting audits, managing documentation, and collaborating on quality agreements. Training and oversight of quality systems are also involved.