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The Engineering Programme Manager will lead the Site Project Department, ensuring regulatory compliance and effective management of project-related activities. Responsibilities include overseeing HR documentation, generating technical solutions, managing training requirements, and coordinating site projects. The role emphasizes maintaining quality standards and integrating new technologies to improve operational efficiency.

The Operations Compliance Coordinator will support investigations of quality events, collaborate with various departments to ensure timely completion of investigations, and manage core systems within the Pharmaceutical Quality System. Responsibilities also include technical writing of standard operating procedures and supporting continuous improvement initiatives.

The AS Team Leader (Dev) is responsible for leading a team within the Analytical Development group, managing team activities, ensuring compliance with regulatory and client requirements, and overseeing method development and validation. The role includes people management, performance appraisals, team training, technical documentation, and project management.

Assist the Quality management team in ensuring compliance with Good Manufacturing Practise standards, interpreting regulations, making quality decisions, and driving quality improvements. Lead audits, documentation review, and compliance enhancement projects. Manage team and drive operational improvements within Quality and Operations departments.

The Qualified Person will implement and manage QP duties and certification activities related to the manufacturing processes at PCI Pharma Services, ensuring compliance with EU GMP standards and other regulatory requirements. Responsibilities include auditing, reviewing documentation, and contributing to quality systems, while also supporting training and process improvement efforts.

Hiring a Quality Assurance Specialist to join the team in Grossbeeren, Germany. Responsibilities include equipment validation, risk analyses, documentation creation, change control, and quality task monitoring. Requires 2-3 years of experience in quality systems, expertise in qualification and validation, GMP training, and fluency in English and German.

Perform analytical testing functions in compliance with procedures and regulations, assist in planning and prioritizing workload, communicate effectively with team members, ensure health and safety procedures are followed, adhere to company guidelines