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The Process Engineer will support technology transfer into manufacturing, collaborate with cross-functional teams, author batch documentation, evaluate processes for improvements, and ensure compliance with GMP manufacturing standards.
The Procurement Specialist will support local and global procurement teams in executing projects focused on cost savings and supplier performance. Responsibilities include collaborating with stakeholders, conducting supplier onboarding, managing contracts, and ensuring alignment with procurement processes to deliver business objectives.
The Group Lead, Quality Assurance Documentation Systems is responsible for leading the Document Control, Records Center, and Systems Administration departments. They facilitate the implementation and maintenance of documentation systems, manage departmental processes, act as a subject matter expert for SOPs, and support regulatory inspections and quality metrics. Leadership experience and a strong background in Quality Assurance are emphasized.
The Principal Scientist will lead technical transfer processes, provide documentation, assess process data, and offer support for manufacturing processes. This role involves collaborating with clients and internal teams to facilitate project progress and improvements in drug substance operations.
The Specialist III, Quality Assurance is responsible for executing internal audits, facilitating customer audits, maintaining licenses, organizing documentation for regulatory submissions, and supporting improvements in the quality system. They must ensure compliance with regulatory requirements and lead initiatives for process improvements across departments.
As a Qualified Person (QP) at Catalent, Bathgate, you will provide QA expertise, certify finished products, review GMP documents, investigate batch release improvements, participate in product recalls, ensure regulatory requirements are met, and identify quality improvements. The role requires Sterile and Biological Product experience, Biotech Products knowledge, and compliance with GMP regulations.
The Global Lean Leader will implement lean methodologies across Catalent sites to improve safety, quality, cost, and delivery metrics. This role involves change management, training, coaching, and conducting workshops to facilitate the adoption of The Catalent Way. Frequent global travel is required to support manufacturing sites in driving continuous improvement initiatives.
The Lead Specialist, QA – Batch Disposition is responsible for providing quality assurance support for GMP documentation and ensuring compliance with regulatory standards. The role involves reviewing manufacturing activity documentation, interacting with the quality team, executing batch record reviews, evaluating product disposition, and compiling performance metrics.
The Principal Quality Assurance Representative will develop and implement sterility assurance and microbiology strategies at a pharmaceutical manufacturing facility, oversee compliance, assist in regulatory inspections, and ensure clean room controls to minimize contamination risks.
The Senior Financial Analyst at Catalent Maryland will analyze past financial performance, provide cost management, and support financial decision-making. The role requires a Bachelor's degree in accounting or finance, at least 3 years of experience, and proficiency in Microsoft Excel.
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