Validation Field Specialist

Join our client's Team as a Validation Technician in the Horsham, PA market. We seek a committed, responsible Validation Technician to supervise and conduct professional, thorough equipment installations and validations within cGMP and non-cGMP facilities.? In this role the validation technician travels (at least 80% of the time) to various life science (pharmaceutical manufacturers, research labs, etc.) and healthcare (hospitals, clinics, etc.) facilities, provides equipment installation and testing services, develops site specific decontamination cycles, conducts equipment integration testing, performs operator training, and authors site-specific SOPs.??The validation technician will be expected to assist in the development of site specific protocols, execute protocols, provide a high level of professional consultation to clients, provide follow-up support to facilities and prepare reports.? The commissioned equipment includes hydrogen peroxide vapor (HPV) gas generators, HPV accessories, aeration units and sensory equipment utilized for the biological decontamination of target areas. Full training for all aspects of the job will be given.What’s in it for You:The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, abundant energy and healthy environmentsPaid training program that includes job shadowing and structured field activities allowing you to learn from subject matter experts with proven successThe ability to make an impact and shape your career with a company that is passionate about growthCompany vehicle provided during working hoursComprehensive benefits package starting day one of employment- medical, dental, vision, matching 401k, company paid pension, stock purchase plan, tuition reimbursement and more!What You Will Do:Assisting in providing information to sales staff regarding site specific equipment and documentation requirements for effective decontamination of target areas and their validation.Working with client representatives to ensure they obtain the correct documentation to achieve goals and certifications required by site.Leading or assisting in the development of job-specific, on-site protocols for the validation work to be carried out on client locations.Collecting site specific information in preparation of equipment installation and commissioning.Maintaining a strong working knowledge of cGMP practices and provide consultation to Bioquell staff on the subjectTraveling extensively (at least 80% of the time) to domestic and international client sites to execute developed protocols including but not limited to:New equipment installation, setup, commissioningEquipment integration testingOperator trainingCalibration on new equipmentTroubleshooting new installations on siteCycle development services on clients sites for cGMP and non-cGMP facilitiesEquipment performance qualificationsReacting to and remedying emergency client requests for information and services in a professional and flexible manner.Providing upkeep to validation equipment to ensure it is in safe working condition.Participating in departmental cross-training with service and RBDS responsibilities to assist in these roles when necessary.Writing and executing material testing protocols as needed for clients requesting this service.Handling micro-organisms as an integral part of verification/validation of the decontamination cycle development process.Collecting and recording site specific data.Generating, reviewing and distributing required site specific reports.Following company policies, procedures and business ethics codes.??Position Details:Work Schedule: Monday to Friday, 40 hours a week, including occasional weekend workWeekend working may be requiredSecurity clearance may be required for certain clientsMinimum Qualifications:Strong background in science, engineering, math or other technical disciplineFull understanding of scientific process with strong analytical abilitiesOutstanding technical aptitude for mechanical and electrical assembliesExcellent troubleshooting abilitiesWorking knowledge of cGMP practicesProfessional, respectful supervisory behaviors and approachWillingness to travel (minimum of 80% of time, with possibility of travel abroad)Responsible, reliable, quality conscious attitude and commitment to job requirements and performancePhysical Demands: Ability to complete pre-employment assessments including a physical, lift and/or carry 50 pounds and drug screenPersonal protection: Personal protection equipment (PPE) may be worn on customer sitesPreferred Qualifications: Bachelor’s Degree in a science discipline or equivalent experience

• *This will be 90% travel, so we're looking for specific people here who are open to this. Travel is within North America, mostly contiguous US, but could be Mexico, Canada, and South America as well. Car and plane travel, they will get a company car for any drives under 5 hours. Norm will be one site per week per engineer, sometimes there is weekend work as needed for client emergencies.