- Veritas Search Group (Boston, MA)
- …not accepted. This role is fully on-site in Boston. POSITION SUMMARY The GMP Quality Engineering and Validation Consultant - CGT QA role is responsible ... materials management, and facility/ engineering functions Support change controls, validation protocols, risk assessments, GMP investigations, and CAPAs… more
- Rhythm Pharmaceuticals (Boston, MA)
- …our Boston or Amsterdam office to play a key role in ensuring quality and regulation-based compliance during the manufacture and distribution of Rhythm clinical and ... be a key team member of the Technical Operations, GMP and GDP QA Group. Their main activities include...Their main activities include managing the day-to-day administration of quality processes and records, ensuring operational excellence in GxP… more
- Stantec (Boston, MA)
- …the designs that support and enhance our communities. The Commissioning and Validation role provides crucial services to confirm equipment and facilities meet the ... hear from you. We have two immediate openings in our Buildings Commissioning/ Validation group for an enthusiastic, diligent and experienced Commissioning / … more
- Integra LifeSciences (Braintree, MA)
- …role is a seasoned professional engineer with complete and in-depth conceptual knowledge of quality engineering . They are knowledge of quality engineering ... over time (where applicable). + Lead implementation of SPC programs with Manufacturing and Quality Control as a part of Process Validation and Design Transfer. +… more
- Integra LifeSciences (Braintree, MA)
- …time (where applicable). + Support implementation of SPC programs with Manufacturing and Quality Control as a part of Process Validation and Design Transfer. ... coordinating efforts for the development and implementation of new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing… more
- Rhythm Pharmaceuticals (Boston, MA)
- …our Boston or Amsterdam office to play a key role in ensuring quality and regulation-based compliance during the manufacture and distribution of Rhythm clinical and ... be a key team member of the Technical Operations, GMP and GDP QA Group. Their main activities include...Their main activities include managing the day-to-day administration of quality processes and records, ensuring operational excellence in GxP… more
- Cognizant (Boston, MA)
- …in cross-functional program leadership meetings, ensuring alignment between automation, process engineering , digital/MES, and quality teams . Serve as the ... technical decision-making. . Clear understanding of automation compliance requirements, including GMP and validation principles. . Excellent communication skills… more
- Takeda Pharmaceuticals (Boston, MA)
- …formulation development, process development, drug product manufacturing, regulatory support, validation thru commercialization of oral drug products for global ... + Writes/reviews/approvesprotocols and reports fordrugproducts + Managesanyreportingstaff(Takeda employeesand/orcontractors). + Preparesorsupervisespreparationofhigh- quality DP-CMCsectionsfor Global regulatory filings to meet accelerated submission… more
- Medtronic (Boston, MA)
- …will work with multiple stakeholders from an all-access position within the Software Engineering Center of Excellence to prioritize and define the scope of the ... functional group of highly talented software developers, test engineers and quality engineers, collaborating with cross-functional teams to develop and design next… more
