Vacancy caducado!
- Supports quality oversight for root-cause analysis and product impact assessment for investigations as a result of deviations, OOS, and OOT investigations ensuring appropriate CAPA actions are identified.
- Supports change control assessments, implementation and closure
- Identifies and facilitates continuous improvement efforts
- Supports drafting and revising Quality Agreements between CMOs/Suppliers, as needed
- Helps represents on cross-functional working teams, applying strong communication and collaboration skills.
- Support continuous improvement projects
- Experience supporting multiple projects/teams within stated objectives and timelines
- Experience supporting cross-functional team members and collaborate effectively
- Good communication skills (written and verbal) and the ability to exchange potentially complex information
- Able to integrates activities with other groups, departments and project teams as needed
- Demonstrated ability to support evaluation of quality matters and solve straightforward problems using technical experience and judgement based on precedent
- Ability to work in a fast-paced environment and meet quality, accuracy, and timeliness objectives
- Expanded conceptual knowledge of cGMP's in a pharmaceutical setting
- Proficient in leading event investigations, Root Cause Analysis (RCA), and CAPA
Vacancy caducado!