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Validation Engineer

Wilson, NC · Manufacturing
Validation Engineer – Triaga Inc.

Be part of a revolutionary change at a Fortune 500 company.
 
At Triaga we’ve chosen to do something incredible. We’re building our future on smoke free products with the power to change the lives of millions of smokers.

With this start up initiative come huge opportunities. So, when ​you join us, you’ll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. It’s so rare in R&D that everything aligns to create the ideal conditions for outstanding work. Right now, at Triaga, that’s exactly what’s happening.
 
By joining our strong Quality/R&D team, you will have the resources, support and technology you need to break new ground and see ideas come to life. You’ll be surrounded by some of the brightest scientists in their fields, backed by extensive investment in R&D, and with fast access to subject matter experts and commercial decision makers.
 
If you’re creative and courageous, you can make a huge impact and propel your career in an endless number of directions. Ultimately, by working on our smoke free future, you can change the lives of millions. 

Your Responsibilities:
  • Lead and execute validation activities that are identified and required. Prepare all the documentation associated by ensuring the execution following the plan. Ensure that all validation activities are carried out and reported in a timely manner. Ensure that all deviations during validation activities are investigated and escalated when required. Propose action plans and ensure that correctives/preventives actions are followed and closed on time.
  • Organize and lead the Continued Verification Assessment and the re-execution of validation protocols according to plan and procedures. Provide reports and other documentation associated with validations, as appropriate for each validation exercise.
  • Lead and coordinate change management process in the factory and ensure validated state of the manufacturing processes, methods and systems is maintained. Ensure the reporting and the update of key metrics.
  • Provide support and act as SME / Facilitator for the Quality Risk Assessment. Ensure the appropriate methodologies are implemented and mitigation plans defined and followed up by the relevant responsible persons as per established quality requirements.
  • Participate to the creation/update of procedures, work instructions and others Quality Documents that are required. Provide support and training by ensuring a transfer of knowledge according to the training management system.
  • Promote and apply all rules concerning PMI Quality, environment, health and safety.
Who we’re looking for:
  • University degree in in Biological Sciences, Physical Sciences, Engineering or equivalent or equivalent skills through demonstrated experience
  • 3-5 years’ experience in quality Assurance in tobacco, food, pharmaceutical or similar industry
  • Advanced knowledge of relevant standards (ISO, ICH, GMP)
  • Well-developed IT skills and project management skills
  • Advanced knowledge on Quality tools, root cause analysis, analytical skills, statistical tool knowledge
  • Fluent in English written and spoken
What we offer:
  • Attractive salary and excellent benefits package: including 401(k) plan, Medical, Dental, and Vision coverage along with paid holidays and three weeks of vacation.
Our success depends on the men and women who come to work every single day with a sense of purpose and an appetite for progress. Join Triaga Inc. and you too can:
  • Seize the freedom to define your future and ours. We’ll empower you to take risks, experiment and explore.
  • Be part of an inclusive, diverse culture, where everyone’s contribution is respected; collaborate with some of the world’s best people and feel like you belong.
  • Pursue your ambitions and develop your skills with a global business – our staggering size and scale provides endless opportunities to progress.
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