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As a Senior Automation Engineer, you will design and implement software/hardware improvements, provide technical support for manufacturing and quality control, troubleshoot automation system deviations, and develop necessary documentation for equipment. You will work in a regulated environment to improve biopharmaceutical manufacturing processes.
The Principal Project Manager - Engineering designs and specifies biopharmaceutical process equipment, manages projects related to these systems, prepares engineering documentation, and supports QA/Validation departments. This role includes overseeing installation, supporting investigations, implementing corrective actions, and may require domestic and international travel.
The Innovation Protection Specialist is responsible for managing medical device development portfolios, focusing on innovation protection strategies, due diligence, and legal agreements. They collaborate with internal teams to support medical device R&D, provide metrics on intellectual property matters, and educate colleagues on compliance processes.
Responsible for delivering complex and strategic IT projects across Applications and Infrastructure for IOPS. Manage project delivery within budget, scope, quality, and time requirements. Communicate with team members and stakeholders to ensure project success. In-depth knowledge of Project Management, SDLC, PM Tools and Processes, Enterprise systems, and Life Sciences environment required.
The Manager Statistical Programming leads programming efforts for clinical study data, ensuring compliance with project standards. Responsibilities include development of analysis tables and managing programming for regulatory submissions. The role requires advanced expertise in SAS and experience with CDISC standards and complex data systems.
The Associate Manager, Research Program Management will oversee the quality and accessibility of scientific project data, ensure data accuracy, manage discovery portfolios, and provide insights for decision-making. This role will also involve improving data management processes and mentoring others in the use of PPM systems and tools.
The Principal GMP Auditor is responsible for managing auditors' training, performing audits, ensuring compliance with GxP regulations, and collaborating with various stakeholders on quality management processes. Duties include maintaining audit documentation, overseeing auditor training programs, and leading supplier audits while ensuring adherence to regulatory standards.
The Sr. Manager Development Program Management leads operational direction for development programs in the drug development industry, managing multiple projects through their lifecycle and collaborating with cross-functional teams. Responsibilities include planning, budget oversight, risk mitigation, and facilitating communication across stakeholders to drive program success from preclinical to commercialization.
The Scientist in Auditory Sciences will conduct basic research on deafness and hearing impairment, performing experiments with animal models, analyzing data, and working collaboratively with a team to advance understanding in the field. Responsibilities include maintaining cultures, characterizing hearing models, and executing experiments involving surgical techniques.
The Manager for Supply Planning oversees the supply chain processes, ensures alignment between demand and supply, leads cross-functional collaboration, manages risks and constraints, and provides leadership to team members. Additionally, the role focuses on process efficiency and strategic planning, supporting operational needs while aligning with company goals.
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