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The Principal Representative, QA will implement and maintain the Data Integrity program, manage System and Validation Lifecycle Documentation, and ensure compliance with GxP standards. Responsibilities include reviewing validation documents and SOPs, performing data integrity assessments, and participating in audit trail reviews.

The Master Scheduler at Catalent is responsible for creating and managing the Master Production Schedule (MPS) as well as the short-term production schedule for the Greendale site. The role involves collaborating with various departments to ensure efficient production planning and schedule execution. The candidate should have a Bachelor's degree with 3+ years of Manufacturing scheduling experience and knowledge of Finite Planning techniques.

The Associate Scientist engages in pharmaceutical development and clinical manufacturing projects, overseeing tasks like formulation, data interpretation, and documentation while ensuring timely execution of responsibilities and ongoing communication with internal teams and clients.

The General Manager is responsible for the overall management, compliance, and profitability of a pharmaceutical development site, focusing on customer satisfaction, operational excellence, and continuous improvement while ensuring adherence to regulatory standards.

The Senior Associate Scientist will conduct experiments, perform analytical product testing, and ensure compliance with regulatory standards. Responsibilities include testing stability samples, conducting laboratory investigations, and data analysis, all while adhering to SOPs and cGMPs.

Experienced Accountant needed to support Biologics businesses at Catalent Pharma Solutions in Cham, Switzerland. Responsibilities include Balance Sheet Reconciliations, Journal Entry preparation, Bank bookings, supplier payments, and proactive process improvement. Requires 2 years of similar experience in the Pharma industry with expertise in G/L and BS, analytical skills, organizational skills, and fluency in English. Competitive salary, pension plan, and personal development opportunities offered.

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.