GMP Operational Quality Senior Specialist - Packaging/Labeling (Contract) 883

The Sr. Specialist GMP QA Operations works with a high degree of independence, while providing oversight of the development, implementation and maintenance of relevant quality initiatives in support of their function. The Senior Specialist completes work in a resourceful, self-sufficient manner and is able to design alternative approaches to achieve desired outcomes. They are adept at troubleshooting problems, coordinating and executing activities on multiple complex projects ensuring alignment with corporate goals and compliance with all regulatory requirements.

• →Master and Executed Batch Record review and resolution of comments/issues
• →Archiving of batch documents in electronic document system
• →Track data for the purpose of metrics generation
• →Evaluations of Investigations/ OOS/ Change Controls to support Disposition Status
• →Disposition Decision and status change in Oracle
• →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 and Vertex, as needed
• →Helps represents Vertex Quality 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

• Bachelor's degree in scientific or allied health field (or equivalent degree)
• Requires experience in batch release, GMP environment, or the equivalent combination of education and experience

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

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If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.