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The Process Scientist I supports transfer and process development activities by collaborating with teams on GMP batch manufacture and optimization, maintaining inventory, and assisting with documentation for regulatory submissions. Responsibilities include planning development batches, writing SOPs, and maintaining accurate documentation in compliance with GMP guidelines.

The Zone Operations Manager oversees the manufacturing team to ensure quality and timely production of pharmaceutical products. They manage technician allocation, ensure compliance with cGMP standards, troubleshoot operational issues, and coordinate with other departments. The role requires effective leadership, performance evaluation, and training execution.

The Quality Assurance Specialist I will oversee the quarantine process, audit production and packaging, review incoming materials, and ensure compliance with quality standards and regulatory requirements, including FDA and cGMP. Responsibilities also include documenting non-compliance issues and participating in training.

The Sr. QC Scientist - LIMS Administration at Catalent Pharma Solutions is responsible for managing accounts and implementing the LabVantage® LIMS at the BWI Harmans site. This role involves providing end-user support, ensuring system compliance, and participating in design modifications.

The Master Scheduler oversees the development and maintenance of the Master Schedule and short-term production schedules for Catalent's Commercial and Development products. They partner with various teams to translate requirements into schedule, monitor daily operations, and facilitate production capacity reviews, ensuring alignment across departments and timely delivery of products.

The Senior Specialist, QA OTF at Catalent is responsible for providing Quality Assurance support for GMP Manufacturing of biological products. This role involves on-the-floor oversight of manufacturing operations, reviewing documentation for compliance, and ensuring systems and procedures are in line with regulatory standards and quality improvements.

The Manager, Quality Systems Audit at Catalent is responsible for managing and overseeing core quality systems including investigation/deviation management, CAPA tracking, change control, risk management, and compiling quality metrics for Senior Management review.