Role: Deviations Specialist (Pharmaceutical) Location: Boston (Seaport), MA Duration: 12+ Months Summary: The... Deviations Specialist will provide investigation and compliance support to a Pharmaceutical Manufacturing Facility. The candidate...
Job Description: The Sr. Quality Specialist is recognized as an expert internally in the principles and application... of quality assurance and compliance. The Sr. Quality Specialist coordinates GMP activities in support of clinical and commercial...
Job Description: The Sr. Quality Specialist is recognized as an expert internally in the principles and application... of quality assurance and compliance. The Sr. Quality Specialist coordinates GMP activities in support of clinical and commercial...
as assigned Review and Approval of Moderate Risk Deviations Demonstrated Subject Matter Expertise in at least one QA functional... and at least five to eight years cGMP experience in a pharmaceutical manufacturing company or equivalent combination of education...
development quality systems such as problem, incident, change, release, deviations, periodic reviews Experience in validation... deliverables, review and approval as a QA Requirements: Experience in the BioTech/Pharmaceutical industry or similar regulated...
, deviations, in-process data, EM data, QC release testing and other quality systems as applicable to determine acceptability... with proficient knowledge of the following in a pharmaceutical setting: Cell and gene therapy cGMP’s and associated CMC regulatory...
records, deviations, in-process data, EM data, QC release testing and other quality systems as applicable to determine... and manufacturing with proficient knowledge of the following in a pharmaceutical setting: Cell and gene therapy cGMP...