Job Description: The Data Entry Specialist is responsible for locating, collecting, transcribing, and verifying batch record data into the Global Data Mart (GDM). This role directly supports MSAT, Process Analytics, Process Validation, and...
Job Description: LabWare LIMS Configuration Specialist to support the LabWare 8 upgrade for a US based GMP laboratory site. This role will lead a dedicated workstream focused on implementing raw material and commercial product workflows, ...
Job Description: LabWare LIMS Configuration Specialist to support the LabWare 8 upgrade for a US based GMP laboratory site. This role will lead a dedicated workstream focused on implementing raw material and commercial product workflows, ...
Roles & Responsibilities Write and execute validation protocols and reports (IQ, OQ, PQ). Develop and implement manufacturing processes, specifications, operator instructions, process studies, and production readiness activities. Conduc...
, and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
Job Description: Contributes within team using SAP, Syncade and/or Ship console Systems for receipt, storage, issuance, dispensing and allocations of API and consumable components. Supports Manufacturing in handling & shipping product dome...
Job Description: The Construction Manager is responsible for leading, coordinating, and overseeing all construction activities for the ECPC project from kick-off to completion. This role acts as the primary liaison between Lonza and the Ge...
Summary : We are seeking an experienced Supplier Quality Engineer with a strong background in the Medical Device industry to support supplier quality, incoming inspection, and manufacturing quality initiatives. Roles & responsibilities :...
Job Description: The Deviation Investigator Level III is responsible for the investigation and completion of deviations aimed at identification of root cause and implementation of correct actions to prevent recurrence. Level III Investigat...
5 to 6 years of Medical Device Supplier Quality experience with Electrical background. Candidates with IPC certifications & Expertise in PCBA inspections. Experience in Interacting with US & Overseas supplier Experience in Supplier Evalua...