Senior Validation Engineer

Job summary
We are seeking CQV Engineers with 4-8 years' experience and we can assist with relocation costs.
Responsibilities
• The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation.• Responsible for protocol writing and execution, field verification, and development of summary reports at the client site.• Planning/coordinating work and directing small teams in document development and/or execution.
Requirements
• BS in a science or engineering field or equivalent years of experience.• 4-8 years' experience in commissioning and/or qualification activities in a regulated industry.• Excellent technical problem-solving and troubleshooting skills.• Solid knowledge of typical project technical issues.• High attention to detail.• Ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines.• Ability to work independently, while quickly building and nurturing a project team.• Expertise in Microsoft Word and Excel.• Familiarity with ISPE Baseline Guide 5 (Second Edition) a plus.• Experience in planning / directing C&Q activities a plus.• Must have experience in 1 or more of the following: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC) upstream, downstream, purification, recovery, building automation or other pharmaceutical manufacturing processes.• Excellent oral and written communication skills in English/Fluent in English.• Able to travel domestically and internationally as required.• Able to work (paid) overtime.• Able to work in the US without sponsorship now or any time in the future.
Benefits
• Our full-time positions offer competitive compensation and benefits which include: up to 15% retirement contribution, 24 days PTO and 5 sick days per year, health insurance at extremely low cost to employee, financial support for both internal and external professional education as well as 70% long term disability paid for by the company.