Company: Piramal Enterprises Ltd.
Key Roles/Responsibilities: All aspects involved in the introduction of repeat processes into Manufacturing, including: Establishing the scope of change for an incoming process through effective communication with the project team/client; Working within the Piramal QMS to initiate, manage, and complete requests for change; Preparing and updating documentation to be used in the GMP manufacture of [...]Read More... from Senior Technical Operations Officer See details
Key Roles/Responsibilities: Execute defined procedures to manufacture high potency ADC/API’s product in support of launched products and clinical trial programs to GMP standards. Work effectively in an organized manner to adhere to the planned schedule. Contribute effectively to a team working environment while also having the ability and confidence to work individually within the production [...]Read More... from Senior Manufacturing Technician See details
Position summary and overview To provide the primary point of contact between the IS Helpdesk and the rest of the IS department and the site internal customers with IS support needs. This will involve an understanding of customer needs and requirements and the ability to provide second or third level configuration problem solving support on [...]Read More... from IS Support Analyst See details
Key Roles/Responsibilities: QA primary point of contact (internal and external) for designated projects. Collaborate with internal and external stakeholders to ensure quality of all product related activities. Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures, Analytical Procedures and associated documentation. Participate in quality related [...]Read More... from QA Officer See details
Key Roles/Responsibilities: Microbiological testing of raw materials, in process, bulk drug substance, final products and stability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFR part11 Good Documentation Practices for Electronic Data. Conduct Environmental Monitoring and associated Identification of isolated micro-organisms. System owners of QC equipment, assisting in equipment periodic reviews, [...]Read More... from QC Micro Analyst See details
Key Roles/Responsibilities: Chief Accountabilities & Responsibilities Laboratory work: Plan and carry out experiments and analysis, as outlined by the project lead, to ensure effective technology transfer and development of fit for purpose processes in line with customer requirements. Record all laboratory work in standard official notebooks and compile results and observations for incorporation into technical [...]Read More... from Protein Scientist See details
