The Business Development Executive will develop and implement sales strategies, manage client relations, and lead contract negotiations to generate revenue growth for Simtra.

The Supply Chain Planner is responsible for creating and maintaining production plans by analyzing capacity and resource needs, collaborating with manufacturing, and managing data integrity in an ERP system.

Oversee design, implementation, and maintenance of process automation systems ensuring compliance with cGMP by optimizing production efficiency and quality control.

The Research Associate II role involves managing analytical method development, validation projects, and supporting formulation development for clients, ensuring compliance with quality standards.

Manage all aseptic operations, ensuring compliance with cGMP regulations and driving team performance while fostering cross-functional relationships.

Oversee onboarding of new projects, manage customer relationships, ensure compliance with project standards, and drive performance improvements in a 10+ project management team.

Manage endpoint devices ensuring security and performance, provide IT support to executives, and lead automation and deployment strategies using Microsoft Intune and SCCM.

The Process Engineer is responsible for optimizing manufacturing and packaging processes, compliant with safety standards, and improving efficiency. Requires collaboration and technical support for operations.

The Senior Process Engineer is responsible for improving equipment and processes, troubleshooting, managing projects, and achieving quality standards in a pharmaceutical manufacturing environment.

The Senior Process Engineer drives continuous improvement, manages equipment reliability, oversees engineering projects, and contributes to production quality needs.

The Talent Acquisition Partner at Simtra BioPharma Solutions is responsible for sourcing, hiring talent, managing recruitment strategies, ensuring a positive candidate experience, and collaborating with business leaders for staffing needs.

The Senior Technical Transfer Associate leads onboarding and process development for drug manufacturing, ensures quality compliance, and provides technical support.

Join Simtra's Talent Community to stay updated on new opportunities in the Contract Development and Manufacturing Organization (CDMO) industry. Be part of various roles and contribute to advancements in R&D, Manufacturing, Quality Assurance, Project Management, and Business Development.

The Senior HRIS Application Analyst will provide leadership in enhancing cloud-based HR applications, including integration, administration, testing, and support to meet user needs.

The Program Manager, Global Learning & Development designs and manages learning programs to enhance leadership, skills, and employee engagement, aligning with business goals.

The Senior Scientist will develop and optimize conjugation and purification platforms, manage a team, ensure compliance with GMP standards, and foster innovation in drug development.

As Manager Business Development, you will drive sales, identify leads, negotiate contracts, and build customer relationships while collaborating with management.

The Junior Development Scientist will manage development projects for injectable products, perform calculations, interpret data, optimize techniques, and enhance department capabilities.