collaborate with research, process development, quality teams, regulatory and CDMOs to ensure a compliant stability program in... addition to providing Quality Control support to ongoing CRISPR Tx programs. Responsibilities Monitor stability program...
group. They will actively collaborate with research, process development, quality teams, regulatory and CDMOs to ensure... a compliant stability program in addition to providing Quality Control support to ongoing CRISPR Tx programs. Responsibilities...
and development of training materials. The Quality Specialist works with a high degree of independence and is adept at troubleshooting...Job Description: The Quality Specialist works cross-functionally to support the training needs of business partners...
Job Description General Summary: The Associate Director, Operational Quality Cell and Gene is recognized... as an expert internally in the principles and application of quality assurance and compliance. The Operational Quality Associate...
We have an exciting opportunity for an experienced Quality Control (QC) professional to join Garuda Therapeutics... at a critical stage in our development as an organization. This position will be based in our Cambridge, MA site, with travel...
Quality Control Analyst I Position Summary: Catalent is a global, high-growth, public company and a leading partner... for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents...
Responsibilities: Manage and coordinate activities associated with the GxP IT Quality Assurance (QA) program for GPS...-regulated industry and preferably in a quality assurance role Highly knowledgeable in Software Lifecycle Development (SDLC...
partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide... unit of its kind for DPI in North America. Catalent Pharma Solutions is hiring a Quality Systems Specialist (Training...
Quality Control Analyst II Position Summary: Catalent is a global, high-growth, public company and a leading... partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide...
development and implementation of a comprehensive quality strategy for a new portfolio of assay products, both centralized... and delivery of program strategy for this new portfolio, provide insights for decision-making, and lead quality assurance...
and testing of clinical-phase cell therapy programs. Independently lead the development of cGMP quality compliance processes... Manager, Cell Therapy Quality Compliance Location: Cambridge, MA About the role: You will report to the Director, Cell...
audit program g) Maintaining KPIs and metrics related to GDP. h) Other tasks as assigned related to GDP Quality Operations...This role, reporting to the Sr. Director Quality Operations, will work in collaboration with GDP and GxP functions...
a positive impact on its customers, employees, and communities. The Role We're hiring experienced Quality Engineers..., including test plans, test cases/scripts, and bug reports assessing quality and associated risk Perform QA activities...
with manufacturing and IVD operations teams within the Quality System Program, including manufacturing process review, batch release...About the Job The Manager, Manufacturing Quality Engineering in the Quality Assurance department is a key...
POSITION SUMMARY: Under the general guidance of the Quality and Compliance Specialist, the Quality and Compliance..., CLIA, CAP and JCAHO, NCCLS, HCFA, OSHA, DPH, the HIPAA, and all payers. The Laboratory Quality and Compliance Coordinator...
for development of pharma R&D platforms; experience with validation/quality compliance requirements. Convey complex information... that all information I submit in my employment application is true to the best of my knowledge. Job Description Job Title: R&D Quality...
R&D archival program, working across the global enterprise with key stakeholders (e.g., in Research, Global Quality... Archivist, Research Quality Location: Cambridge, MA About the role: The Principal Archivist is a member of the Research...
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...
inspection functions and activities in conformance with the company’s Quality Program. Quality Engineer Required Qualifications...Job Overview Skanska is searching for a dynamic Quality Engineer. This is a great opportunity to start a career...
Job Description GENERAL/POSITION SUMMARY The Quality Manager is responsible for managing multiple department... activities with a high degree of independence, while providing oversight of the development, implementation and maintenance...