Job Description: Carries out the practical work in the laboratory including method development, method validation and trouble shooting. Takes over responsibility for the QC part of projects. Perform required testing on raw materials, inter...
Responsibilities: 1. Testing and Validation: Plan and conduct functional tests and performance evaluations on hardware prototypes. Identify and troubleshoot issues related to hardware functionality and compatibility. Collaborate with so...
Responsibilities: Lead end-to-end program strategy, planning, and execution. Manage client relationships and drive business development. Ensure operational excellence and financial oversight. Mentor and manage cross-functional engineer...
Job Description: The Project Manager will be responsible for leading cross-functional projects to support operations, manufacturing, and supply chain initiatives, with a strong preference for experience in the medical devices industry. The...
Job Summary : We are seeking an experienced MES Engineer with strong Pharma domain experience to support and enhance Rockwell Automation Pharma Suite (Factory Talk Production Centre) in a regulated manufacturing environment. The ideal cand...
Job Description: The Project Manager will be responsible for leading cross-functional projects to support operations, manufacturing, and supply chain initiatives, with a strong preference for experience in the medical devices industry. The...
Job Summary: The Process Engineer reports to the Manufacturing Unit Technical Leader and is responsible for driving engineering process improvements, capital equipment upgrades, efficiency gains, and cost reduction initiatives. The role...
Job Description: The GMP Asset Mechanic is responsible to ensure that GMP production assets are evaluated prior to purchase, qualified and documented as needed, maintained and commissioned prior to use, and properly decommissioned and stor...
readiness team in a timely and professional manner. Requirements: Bachelor's degree in a scientific discipline such as life... sciences, pharmacy, bioscience;advanced degree preferred. 5+years of experience in regulatory affairs within the...
Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Cre...