QA Manager

At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 95 years ,we continuously innovate. We dedicate 10% of our revenue to Research & Development such as to improve the diagnosis, prognosis and quality of life of patients.Achieve, Cooperate, Care and Innovate are the values ​​that we share and practice on a daily basis.Working at Guerbet is not only being part of a multicultural team of 2,600 people across more than 20 countries, but, it is above all about playing a unique role in the future of medical imaging.For more information on Guerbet, go to and follow Guerbet on Linkedin, Twitter, Instagram and YoutubeWHAT WE ARE LOOKING FORGuerbet is looking for a qualified, dynamic QA Manager to enhance our quality management system through comprehensive SOP development, review, and revision, ensuring compliance with FDA regulations including CFR (Code of Federal Regulations), ISO standards, industry best practices, as well as all applicable legislative requirements for the company’s product portfolio.Working with cross-functional teams, you will have to be an excellent communicator and will be responsible for ensuring that all projects have the appropriate local quality and safety input and guidance. Implementation and maintenance of an audit and quality assurance system at the local level aligned with the Policies of the Group.YOUR ROLEGeneralEnsure good relations and communications with all members of the team and responding respectfully and in a timely fashion to internal and external customers.Interact influentially with all members of staff to maintain and develop a positive progressive Quality culture throughout the organization.Perform other duties as assigned by management.Quality AssuranceEnsure compliance with the legislative requirements as set out by FDA (21 CFR 314, 21 CFR 820, 21 CFR 822) and PIC/S PE 011-1, as well as all applicable legislative requirements for the company’s product portfolio.Ensure that all third-party contractors are legally approved, and the applicable Technical Quality Agreements (TQA) are in place.Prepare and act as signatory in quality agreements (intercompany and external).Ensure the implementation of ISO 13485:2016 requirements for a quality management system where the organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.Ensure that the business complies with cGxP requirements.Be able to retrieve product traceability and ensure recall readinessResponsible to attend and support regulatory body inspections (For example-FDA, state agencies or any other health authority) at Guerbet LLC level.Ensure of the conformity of fully finished imported pharmaceutical product and release for the US market.Perform the Product Quality Review system by reviewing PQRs and engaging with relevant departments to address recommendations and outstanding information.Oversee the Customer Complaints system and facilitate investigations to establish root cause and work with cross functional teams to facilitate the resolution of the customer complaints.Administration and monitor the QMS, including SOPs, quality management meetings, change controls, deviations, quality risk assessments, customer complaints, recalls, adulteration or counterfeiting investigations, periodic reviews, self-inspection and external audit reports.Facilitate follow-up meetings to discuss the audit findings, clarify questions, and agree on timelines for implementing of the corrective action plans.Ensure any updates and reviews of SOPs are documented and stored in a controlled system and ensure compliance with Global SOPs and with regulatory standards across various operations within the organization.Cooperate with Training Responsible to ensure the appropriate training of the staff. Provide quality support for assistance with Request For Quotation (RFQ) documents and processes.Supervise supply chain activities pertaining to Guerbet pharmaceuticals and medical devices performed by the third-party logistics. Ensure that these activities are performed in compliance with the local legislation and regulations.Ensure Guerbet products are only supplied to persons who are authorised or entitled to supply medicinal products to the public, through the customer qualification process.Inspection & audits Implement all necessary tools to evaluate the quality of the local processes and activities.Conduct/assist with internal self-inspection audits and complete response report.Coordinate, evaluate and follow up on CAPAs related to audit and inspection findings until implementation of CAPA supported by acceptable evidence for critical and major findings.Analyze audit findings, identify areas for improvement and communicate trends to senior management.Maintain high level of awareness and expertise in international regulations so as to ensure appropriate regulatory surveillanceYOUR BACKGROUNDMinimum of 8 years of QA experience in the pharmaceutical/medical device industryAdvanced degree in a relevant field (Chemistry, Engineering, Life Sciences)Demonstrated expertise in FDA regulations and ISO standardsExperience with electronic quality management systemsStrong technical writing and process development skillsPrevious consulting experience in SOP developmentProven experience in audit management and non-conformity resolution.Knowledge of document management/quality systemsExperience with FDA inspectionsKnowledge of radiology environment (preferred)Soft Skills/QualificationsExcellent communication and project management skills.Ability to work independently and as part of a team.Interviewing and presentation skillsStrong and effective communication and interpersonal skillsExcellent analytical, problem solving and decision-making skillsAttention to detail, initiative, confidentiality, customer focused, logical thinking, information seeking and sense of urgencySupervisory skillsExcellent computer skillsWe offer continued personal development. When you join Guerbet, you :Are choosing a global leader with recognized expertise in diagnostic and interventional imaging, Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient’s life all over the world,Are joining a company where we value diversity of talents coming from various horizon.We # Innovate # Cooperate # Care #Achieve at Guerbet. Guerbet is an Equal Opportunity Employer. As an organization, we believe that no individual should be discriminated against because of their differences, which includes the following: age, disability, ethnicity, gender, gender identity and expression, religion, or sexual orientation. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, or any other basis as protected by federal, state, or local law. Guerbet is committed to diversity, equity, and inclusion.Guerbet provides accommodations to applicants and employees with disabilities. If you need an accommodation to apply for a position please send an email to View email address on us.fitly.work or you can also call this number View phone number on us.fitly.work