Omniabio
Position Summary: As the Associate I, Quality Control at OmniaBio, you are a motivated individual with a keen interest in the field of quality control (QC) for Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products, driven by…
Role Summary: OmniaBio is seeking a detail oriented and agile Batch Release Specialist to join our Project Management group. This role is pivotal in coordinating the batch release process for cell and gene therapy products with short shelf lives. The…
Position Summary: As the Associate II, Quality Assurance (QA), at OmniaBio, you are an experienced individual in the field of Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products who is driven by the opportunity to enable clinical…
Position Summary: As Associate I, Quality Assurance (QA), at OmniaBio, you are a motivated individual in the field of Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products who is driven by the opportunity to enable clinical translation…
Position summary At OmniaBio, we rely on a meticulously prepared financial data to drive our business forward. The Accounts Payable Specialist keeps that system running smoothly by supporting the management of our cash flows through accurate recording and tracking of…
Position Summary As a Scientific Lead, MSAT, you will oversee cell and gene therapy Good Manufacturing Practices (GMP) Manufacturing Science and Technology (MSAT) activities, which include technology transfer, process optimization and validation. This position will also provide leadership and support…
Position Summary: As Associate I, Quality Assurance (QA), at OmniaBio, you are a motivated individual in the field of Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products who is driven by the opportunity to enable clinical translation…
Position Summary The Associate II, Commissioning, Qualification and Validation, supports activities including development of validation master plan(s), and qualification/validation of deliverable(s) and standard operating procedures (SOPs). Responsibilities include assessment and development of qualification documentation for the facility, equipment, and systems,…
Position Summary: As the Raw Materials Associate I, Quality Control at OmniaBio, you are a motivated individual in the field of Quality Control for Good Manufacturing Practices (GMP) manufacturing. The Quality Control (QC) team is responsible for all aspect of…