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The MS&T Engineer II/III supports technical processes in a cGMP manufacturing environment, focusing on tech transfers, process engineering, and validation. Responsibilities include documenting processes, conducting investigations on deviations, analyzing data, and collaborating across departments to ensure compliance and quality in biopharmaceutical production.
The Senior Program Manager will oversee project teams, manage client relationships, ensure project timelines and budgets are met, and provide mentorship. Responsibilities include facilitating meetings, analyzing risks, and maintaining high-quality standards in project execution, while collaborating with cross-functional teams and managing financial aspects of projects.
The Senior Accountant is responsible for ensuring the accuracy and completeness of the company's financial statements. Responsibilities include performing monthly closing procedures, analyzing accrual transactions, collaborating with project managers on accounting issues, supporting tax compliance efforts, participating in process improvements, and working with auditors to provide documentation. Special projects and administrative tasks are also part of the role.
The Principal QA Specialist oversees the coordination and management of Deviations and CAPAs within the AFS department, ensuring compliance with GMP activities. This role involves reviewing and approving testing data, method qualifications, and laboratory investigations, collaborating closely with QA and testing groups.
The Senior QC Analyst position involves conducting analytical testing, ensuring compliance with regulatory standards, organizing and processing samples, performing method validation, and supporting laboratory investigations. The analyst also engages in trend analysis, updates SOPs, and leads or participates in continuous improvement projects, maintaining safety and regulatory readiness at all times.
The MS&T Engineer I will apply engineering principles to problem-solve and drive projects to completion, manage multiple projects, and support customer site visits, process data compilation, troubleshooting efforts, and assist in tech transfer programs. Strong communication and project management skills are essential.
Responsible for compliance review of biopharmaceutical development GMP data, including the review and approval of release, in-process, and stability test data, method qualifications, validations, and laboratory investigations and deviations.
The VP of Strategic Marketing will lead the marketing strategy development and execution to enhance brand visibility and drive growth. Responsibilities include overseeing marketing campaigns, collaborating with cross-functional teams, monitoring performance metrics, and managing the marketing team while ensuring compliance with regulations.
The Scientist II is responsible for supporting biopharmaceutical product characterization by performing mass spectrometry and various biochemical techniques. The role includes managing projects, mentoring junior staff, ensuring compliance with regulatory standards, and producing high-quality documentation while maintaining effective communication with clients and team collaboration.
The Research Associate I executes experimental protocols and performs data analysis in biopharmaceutical laboratories, testing drug substance and formulation samples using various bio-analytical techniques while ensuring proper safety and compliance standards.
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