Validation Specialist in Victoria

VALIDATION SPECIALIST Purolite, an Ecolab company, the world leader in resin-based separation, purification and extraction technology, is seeking a VALIDATION SPECIALIST at our state-of-the-art manufacturing site in Victoria, Brasov!At Purolite, we manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It’s an exciting business which helps make the world cleaner, safer and healthier. What you’ll do: Responsible for establishment of Validation/Verification programs spanning pharmaceutical, life science, and industrial products;Creates, reviews, and approves general and operating procedures, work instructions and other quality-related documents;Acts as subject matter expert in no less than one discipline of validation.Develops and maintains validation metrics and ensures compliance and identification of trends leading to site/process/product improvements;Works with Manufacturing, Technical Operations, Engineering, Quality, and R&D teams to implement and execute validation programs;Recommends measures to improve products and process through validation programs;Recommends and implements changes in working conditions and use of equipment to increase efficiency of the department;Contributes to the Quality Management Review and to Change Control programs though direct and indirect engagement with data trending, reference documents, and continuous improvement recommendations;Communicates all deviations and non-conformances to plant management and senior leadership as needed; What you’ll need: Degree in Chemistry, Biochemistry or related subject;Minimum five years Quality (QA and/or QC) experience required;Must have hands-on broad validation experience, knowledge of validation programs in areas of Cleaning, Analytical, Equipment, Process, Environmental, and Computer Systems;Computer literate with advanced writing skills;Must be able to communicate in English with visitors, vendor, professionals, and plant personnel;Must be capable of working in a matrix environment and must possess strong influencing and communication skills;Knowledge of quality assurance requirements for pharmaceuticals: 21 CFR Parts 210/211, ISO 9001, ICH and other standard requirements;Needs to show scientific curiosity and learning agility. What’s in it For You: The opportunity to take on some of the world’s most meaningful challenges, providing sustainable solutions for our environment, businesses and healthcare;The ability to make an impact and shape your career with a company that is passionate about growth;The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best;Comprehensive benefits package. #li-eu Our Commitment to Diversity and InclusionAt Ecolab, we believe the best teams are diverse and inclusive, and we are on a journey to create a workplace where every associate can grow and achieve their best. We are committed to fair and equal treatment of associates and applicants. We recruit, hire, promote, transfer and provide opportunities for advancement on the basis of individual qualifications and job performance. In all matters affecting employment, compensation, benefits, working conditions, and opportunities for advancement, we will not discriminate against any associate or applicant for employment because of race, religion, color, creed, national origin, citizenship status, sex, sexual orientation, gender identity and expressions, genetic information, marital status, age, disability, or status as a covered veteran.In addition, we are committed to furthering the principles of Equal Employment Opportunity (EEO) through Affirmative Action (AA). Our goal is to fully utilize minority, female, disabled and covered veteran individuals at all levels of the workforce. Ecolab is a place where you can grow your career, own your future and impact what matters.


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