Join to apply for the QC Validation Technician role at Syntegon Telstar.2 weeks ago Be among the first 25 applicantsSyntegon Telstar S.R.U is a company within the Syntegon group, operating worldwide.As a brand specialized in developing GMP projects in consulting, engineering, construction, and integrated process equipment, we serve companies in the life sciences market (pharmaceutical, biotechnological, healthcare, cosmetic, veterinary, and food industries), as well as hospitals, laboratories, and research centers. We also offer solutions with vacuum and high vacuum technologies for traditional and high-tech industries in energy and aerospace sectors, including scientific experimentation.Your dutiesWe are looking for a QC Validation Technician for our Terrassa office, with at least 3 years of experience in a similar role, to control, manage, and execute qualifications of special and serial equipment, and defend the projects assigned both at Telstar and at the client's site if necessary.Availability to travel 15-20% across Europe and internationally is required, depending on projects.If this offer matches your personal and professional expectations and you believe you meet the requirements, do not hesitate to apply. We are waiting for you!Responsibilities:
Project Documentation ManagementDesign and develop validation protocols for equipment according to GMPs and client and Telstar quality system requirements.Obtain client approval for protocols and related documentation.Manage and follow up on project change controls.Execute protocols, review results performed by other departments, and related documentation such as certificates.Project Execution ManagementParticipate in project kick-off, monitoring, and closing meetings.Plan and execute qualification tests for special and serial equipment, considering project timelines.Monitor hours spent on tasks and compare with the project budget, justifying deviations.Ensure compliance with project QGs and follow corrective and preventive actions for Special Authorizations.Deviations and Change Controls ManagementDevelop and close deviations.Follow up on corrective and preventive actions related to equipment testing.Manage incident resolution and change controls related to the project.Your profileEducation:
University degree in scientific-technical fields (chemical sciences, pharmacy, biology, engineering, etc.) and/or relevant professional experience.English B2 spoken and written.Experience:
Level 1:
Minimum 3 years of autonomous qualification protocol execution in pharmaceutical equipment;
3 years of project management with end clients and/or commissioning.Level 2:
Minimum 3 years of qualification protocol execution in pharmaceutical equipment or related qualification departments.Additional requirements:
Driver's license and own vehicle.Availability to travel 15-20% across Europe and internationally depending on projects.Syntegon and its subsidiaries promote diversity and are committed to an equitable environment for all employees, regardless of gender, age, origin, religion, sexual orientation, gender identity, or special needs. The masculine form used in this job offer is for readability and refers to individuals of all genders.
#J-18808-Ljbffr