Job Title : Validation Engineer
Location : Boston, MA (Need Local)
Duration : 24+ Months (Contract)
Interview : Video (2 Rounds)
Visa - USC & GC Only
Job Description :
KEY RESPONSIBILITIES :
- Draft and implement Quality System documentation designed to establish good validation practices within the organization.
- Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards.
- Conduct Automation Assessments to ensure compliance with 21 CFR Part 11.
- Coordinate with vendor personnel to schedule and execute of test plans, if required.
- Coordinates with the internal stakeholders to safely and effectively schedule CQV activities, whenever required.
- Effectively works with cross departmental stakeholders, including but not limited to information services, EH&S, Global Security, design teams, and quality.
- Author documents related to or support process validation related activities that include but not limited to aseptic process simulations (APS), process performance qualification, material qualifications, etc.
- Develop cycles for sterilization processes and validate them, if required.
- Completes Vertex assigned training and ensures that they are 100% compliant 100% of the time .
- Ensure that all Validation activities align with the current Vertex SOPs, global standards and cGMP guidelines.
- Supports right-the-first time culture for all documents distributed across the organization. Ensure the VCGT Validation team reputation and partnership is flourished with the cross-functional teams.