Validation Engineer (Contract) 849

The Validation Engineer will report to the VCGT Validation leadership or an appropriate designee to execute Commissioning, Qualification and Validation activities for Vertex’s Cell and Gene Therapies Facility in one of their facilities located in South Boston and Cambridge.

** The ideal candidate will have 1-3 years experience in aseptic operations and validation (at a systems level) ***

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.
• Support all stages of qualification of Analytical Instrument and Manufacturing equipment.
• Support all stages of qualification of automated manufacturing equipment
• Conduct Analytical Instrumentation Qualifications in accordance with USP<1058> and Vertex SOPs.
• 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.

IDEAL CANDIDATES:

• Demonstrated ability to safely execute Validation activities in a dynamic fast paced environment.
• Experience developing and executing Validation protocols in a GMP Manufacturing and Analytical Laboratory areas.
• Receptive to change – Adapts (quickly) to changing circumstances.
• Flexibility for off-shift hours, including weekend and night shift work.
• A, B.S. in Engineering or related discipline with 1-3 years of Validation experience or equivalent professional experience.
• Understanding and application of technical principles, theories, and concepts in the field, GMP, ISO, GAMP, ANSI.

$55-$60/hr

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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