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The Accounting Manager will oversee inventory accounting processes, manage daily accounting activities, month-end close, payroll, and budgets, ensure compliance with US GAAP, and collaborate with various departments to enhance efficiency and accuracy in financial reporting.
The Technology Transfer Scientist I is responsible for ensuring smooth transitions of viral vector processes to manufacturing. This involves document management, analyzing process performance, and working with cross-functional teams to ensure compliance with regulatory standards while optimizing processes. The role requires strong organizational skills and technical expertise.
The Sourcing and Procurement Supervisor ensures timely procurement of compliant materials, supports purchasing activities, manages vendor relationships, and leads a team to optimize inventory cost. This role collaborates with various internal functions while adhering to cGMP guidelines and standards.
The Supply Chain Planner/Scheduler is responsible for demand planning, inventory management, and ensuring quality and timely delivery of products. The role involves creating detailed plans and schedules, overseeing purchasing cycles, and providing direction to manufacturing teams.
The Quality Systems Lead will enhance the Quality Management System (QMS), focusing on electronic support, risk assessments, inspection readiness, and compliance. Responsibilities include managing the QMS platform, facilitating training, conducting audits, and supporting continuous improvement initiatives. The role demands a proactive individual to ensure regulatory compliance and improve quality systems across the organization.
The Automation Engineer II handles the administration of facilities and process automation, providing support and troubleshooting services. Responsibilities include designing and implementing automation systems, leading projects for equipment modifications, and developing test scripts and automation procedures.
The QC Analyst I is responsible for routine and non-routine QC testing per SOPs, conducting analytical testing and managing quality systems including deviations and CAPAs in compliance with cGMP guidelines.
The Process Engineer will manage engineering projects for gene therapy processes, focusing on workflow optimization, compliance with FDA and EU standards, and continuous improvements. Responsibilities include project management, quality control, and ensuring adherence to safety and environmental protocols while driving operational efficiency.
The role involves directing the development of upstream processes for viral vector production, optimizing processes for robustness and yield, and ensuring compliance with GMP standards. Responsibilities include experiment design, monitoring performance, and maintaining relationships with stakeholders and suppliers.
The Quality Operations Associate will oversee quality assurance processes within manufacturing and quality control areas, ensuring compliance with regulations and internal policies. Responsibilities include quality oversight during operations, SOP development, documentation accuracy review, and providing training on GMP and GDP. The role also involves conducting root cause analysis of quality events and collaborating with various departments for quality assurance.
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