Job Description
Title: Validation Engineer
Location: Boston Onsite, Leiden Center
Duration: 6m+
There are 3 roles open here – 2 beginner level (not entirely green but 1-2 yrs is fine) and 1 intermediate level (4+ yrs)
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 assigned training and ensures that they are 100% compliant 100% of the time.
- Ensure that all Validation activities align with the current SOPs, global standards and cGMP guidelines.
- Supports right-the-first time culture for all documents distributed across the organization. Ensure the 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.
- B.A, B.S. in Engineering or related discipline with 5-8 years of Validation experience or equivalent professional experience.
- Understanding and application of technical principles, theories, and concepts in the field, GMP, ISO, GAMP, ANSI.