Show a strong dedication and quick response to internal and external collaboratorsEnsure outstanding conformance to quality systems, including ISO 9001 and cGMPDevelop, deliver, manage, and continuously improve the site master validation and metrology programsAssist with engineering responsibilitiesCommunicate effectively with operational teams to resolve quality procedural and validation variancesHead and engage in quality advancement endeavors related to validations and engineeringEngage actively in audits conducted by customers and regulatory authorities.Carry out tasks in compliance with procedures to meet quality objectivesContribute efficiently to quality advancement teams and foster teamwork between different departmentsPersonal Attributes & Skills Required
Bachelor's degree in a scientific/engineering field or equivalent experienceDesired background includes prior experience as a validation technician within a cGMP or analogous regulatory setting, particularly within the biopharmaceutical, pharmaceutical, or dairy sectors.A strong background in production process and/or manufacturing engineeringTechnical knowledge in cGMP validation concepts and techniquesHighly self-directed, results-focused, and a great teammate with strong communication skillsWorking Conditions
Work in a manufacturing and laboratory and office environmentStand for long periods while performing dutiesWork safely with chemicals, biologics, and hazardous materialsWork overtime when required, with some 24-hour on-call dutiesOccasional travel may be requiredWhat’s in it for you?
Challenging and interesting tasks with problem-solving opportunitiesA variety of tasks and projects to improve your skillsOpportunities to improve systems and processesGrowth in your knowledge of Validation and Facility/Process EngineeringCollaboration with a diverse range of people across multiple departmentsEngage with a large multinational company with global connections and opportunitiesBenefits
Join our team and take advantage of these great benefits!