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The Technical Services Director oversees technical transfer and validation operations, ensuring compliance and leading cross-functional teams to enhance aseptic manufacturing processes.

The Manufacturing Technical Services Representative manages commercial master batch records, trains staff, investigates non-conformance, and collaborates with multiple teams on projects.

The CAPA Manager oversees the Corrective and Preventive Action system ensuring compliance with regulations, leads investigations, analyzes quality data, and collaborates with cross-functional teams to enhance quality performance.

The Automation Engineer is responsible for designing, implementing, optimizing, and maintaining automation systems in pharmaceutical processing, ensuring compliance and efficiency in operations.

The Principal Technical Transfer Representative leads onboarding and process development for new drug products, collaborating with cross-functional teams and providing technical support. Responsibilities include technical documentation, investigations, audits, and mentorship.

The Process Engineer will develop, implement and optimize manufacturing packaging processes, ensuring regulatory compliance and improving efficiency in aseptic manufacturing.

Lead design, implementation, optimization, and maintenance of process automation and controls for pharmaceutical manufacturing. Develop and troubleshoot PLC/HMI programs, deploy full system lifecycle, conduct risk assessments, support validation, and drive automation improvement projects.

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The Project Manager leads new business initiatives in pharmaceutical product development, ensuring project milestones, client expectations, and regulatory compliance in collaboration with various teams and stakeholders.

The Senior Technical Transfer Associate leads onboarding and process development for new drug products at Simtra, collaborating with cross-functional teams and ensuring compliance with quality standards.