Provide a variety of analytical functions that occur in the QC department supporting validation, testing and reporting of in-process, release and stability samples. Ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values. Serve as RSL representative in cross-functional, cross-departmental working teams and/or working with outside vendors to meet all laboratory needs. Coordinate and facilitate laboratory activities to meet commitments on-time. Maintain accurate laboratory records and adhere to cGMP/GDP expectations. Participate in planning, executing and/or review of method validations, method transfers and/or equipment qualification/requalification Assist in troubleshooting of analytical methods and/or equipment as required. Authors, reviews, and/or approve data, SOPs, COAs, analytical methods, protocols and reports. Lead compliance related teams working towards the goal of continuous improvement. Perform in-process, release, and stability testing and/or review independently following established methodology, procedures and SOPs. Lead the OOS/OOT investigations/deviations and to identify corrective actions to prevent reoccurrence.