We are currently looking to fill a Quality Assurance Specialist (Drug Product) position. This position will support... Quality Assurance initiatives for a broad range of topics relative to the start-up and operations of a Drug Product facility...
to support their operations. Job Description This is a full-time onsite QA Specialist I position located in Morrisville, NC... of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials...
The Lead Specialist, QA is responsible for providing QA lead support and oversight of Client Projects from start... to finish for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product. The...
Johnson & Johnson is currently seeking a QA Specialist II to join our QA team located in Raritan, NJ! At Johnson... including preparation of product release documentation. Partner with Operations teams to support production activities...
Senior Specialist, QA – Batch Disposition Position Summary Catalent, Inc. is a leading global contract development... technologies, including AAV and other viral vectors, vaccines, and oncolytic immunotherapies. The Senior Specialist, QA – Batch...
Senior Specialist, QA – Batch Disposition Position Summary Catalent, Inc. is a leading global contract development... technologies, including AAV and other viral vectors, vaccines, and oncolytic immunotherapies. The Senior Specialist, QA – Batch...
lives. Read more: . Position: Sr. Specialist, Quality Assurance Operations Location: Warren, NJ The Sr. Specialist, QA... Shop Floor and Warren Site Walkthrough activities, Label Printing and Issuance of finished drug product and shipping labels...
Senior Specialist, QA – Batch Disposition Position Summary Catalent, Inc. is a leading global contract development...-based therapies and vaccines. The Senior Specialist, QA – Batch Disposition is responsible for providing Quality Assurance...
Senior Specialist, QA – Batch Disposition Position Summary Catalent, Inc. is a leading global contract development...-based therapies and vaccines. The Senior Specialist, QA – Batch Disposition is responsible for providing Quality Assurance...
Senior Specialist, QA – Batch Disposition Position Summary Catalent, Inc. is a leading global contract development...-based therapies and vaccines. The Senior Specialist, QA – Batch Disposition is responsible for providing Quality Assurance...
Senior Specialist, QA – Batch Disposition Position Summary Catalent, Inc. is a leading global contract development...-based therapies and vaccines. The Senior Specialist, QA – Batch Disposition is responsible for providing Quality Assurance...
and the following amount of relevant experience for each level: Associate QA Specialist – 2+ years QA Specialist – 4...+ years Senior QA Specialist - 6+ uears May substitute proven experience for education requirement. Level is determined...
Lead Specialist, QA Batch Disposition Position Summary Catalent, Inc. is a leading global contract development...-based therapies and vaccines. The Lead Specialist, QA – Batch Disposition is responsible for providing Quality Assurance...
% inspection Parenteral product units.The QA Specialist – Stat Sort provides support to Operations related to final classification.... Role Description: The QA Specialist – Stat Sort is responsible for providing manual visual inspection of the 100...
Overview The QA Specialist III, QA Compliance, will be responsible for the review and approval of commissioning... for Quality Assurance. The QA Compliance Specialist III, QA Compliance, will handle all associated responsibilities in compliance...
Siegfried an attractive employer. Your role The QA Documentation Specialist will support the QA Department with all Document.... What we do in Irvine Irvine is one of Siegfried's sterile drug product manufacturing sites, providing contract development...
Overview: The QA Specialist III, QA Compliance, will be responsible for the review and approval of commissioning... for Quality Assurance. The QA Compliance Specialist III, QA Compliance, will handle all associated responsibilities in compliance...
Job Title: QA Engineering Specialist Duration: 08 Month Contract (Possible extension based on work performance... Therapy Development early clinical drug product manufacturing facility, which supplies autologous and allogeneic cell...
QA RA Compliance Specialist ONSITE POSITION - SHIFT - MON-FRI - 8AM - 5PM OR 9AM - 6PM. Coordinate, Track, and Trend... and submission of A/NDA submissions (initial, amendments, supplements, annual reports, 15-day Alert Reports);drug master files...
QA RA Compliance Specialist ONSITE POSITION - SHIFT - MON-FRI - 8AM - 5PM OR 9AM - 6PM. Coordinate, Track, and Trend... and submission of A/NDA submissions (initial, amendments, supplements, annual reports, 15-day Alert Reports);drug master files...