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The Program Manager will oversee cross-functional teams to deliver project outputs on time and within budget, while ensuring quality results. Responsibilities include client relationship management, managing project timelines, facilitating team meetings, analyzing risks, and managing financial aspects of projects. The role demands strong leadership and the ability to motivate teams without direct authority.

The Senior Manager of Quality Assurance oversees the deviations, CAPA and complaints quality systems, managing a team while providing QA support and training. The role includes tracking quality metrics, leading investigations, developing training materials, and facilitating client communications regarding quality-related events.

The Senior Quality Assurance Specialist is responsible for overseeing the review and approval processes for Deviations, CAPAs, and Effectiveness Checks in compliance with cGMP requirements. This role involves collaboration with multiple departments to ensure timely resolution of compliance issues, development of training materials, metrics generation, and mentoring of junior staff.

The Financial Analyst will conduct financial analysis, support month-end close processes, perform account reconciliations, and handle billing issues. Responsibilities include preparing invoices, maintaining customer records, collaborating with accounting teams, and implementing ERP systems. The role requires reviewing billing data, generating reports, and providing customer service.

The MS&T Senior Engineer provides technical support for cGMP production, focusing on tech transfers, process engineering, and validation. This role also includes managing equipment systems and leading cross-functional teams to ensure compliance and successful execution of processes.

The In-Process Support Associate will conduct analytical support for biopharmaceutical processes, particularly focusing on in-process and release testing using bio-analytical techniques like HPLC and UV-Vis. Responsibilities include data analysis, troubleshooting, documentation upkeep, and adherence to safety procedures. The candidate must have a strong protein chemistry background and will be expected to be flexible with work hours as needed.

The Senior Proposal Development Manager writes and edits technical proposals and project plans for biopharmaceutical services, collaborating with various teams to define project scope, schedule, and costs. Responsibilities include reviewing client RFPs, developing proposals, ensuring accuracy, maintaining quality standards, meeting deadlines, and representing KBI's technical capabilities to clients.