BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.
When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:Under the guidance of the local Director Regulatory Affairs, Quality Assurance and Compliance for Spain and Portugal, this position will provide local support on these matters.
Essential Functions of the job:Participation and contribution in local Regulatory Affairs activities for Spain and Portugal.Support the local direction of the Department to guarantee permanent alignment with EU and local regulatory legislation and company rules.Ability to keep fluent interactions with local stakeholders in Spain and Portugal including MoH authorities, Spanish Medicine Agency, and Infarmed.Participation in the regulatory review and approval of local versions of SmPC, labels, and package leaflets and prepare and review information to include on promotional materials.Contribute to the preparation and submission of local regulatory agency applications and reports and provide responses to regulatory authorities to ensure timeliness, accuracy, comprehensiveness, or compliance with regulatory standards.Perform the local review and approval of promotional and non-promotional materials used in Spain and Portugal and submission to authorities where applicable, in alignment with Farmaindustria and Apifarma Codes and company rules.Responsible for the implementation of the approved labels and PL changes in the commercial artworks.Participation and contribution in local Quality Assurance activities for Spain and Portugal.Support the function in Spain and Portugal to build up a local quality management system as required by local regulations.Perform review and approval of local customers.Support local director of the department for product complaints, product recalls, deviations, change controls, destructions, returns, mock-recalls, and serialization matters.Collaboration to develop, maintain, and validate standard operating procedures or local working practices, and ensure compliance.Collaboration in local quality agreement with the LSP.Participation and contribution in local Compliance activities for Spain and Portugal.Collaboration in local development of processes and procedures needed.Participation in local industry working group meetings.Collaboration in training new starters in alignment with local Codes and Company rules.Contribution to annual live Monitoring and Auditing exercise on local activities, as per Monitoring and Auditing checklist.Collaboration in the compliance advice for local and international events in Spain and Portugal.Education Required:University degree in life science / pharmacy
Experience Required:5+ years of experience in the pharmaceutical industry.
Computer Skills:Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint, and Outlook.
Other Qualifications:Ability to work effectively in a fast-paced environment.
Good interpersonal and collaborative skills, strong organizational skills, and effective written and verbal communication skills.
Travel:Up to 10%
BeiGene Global Competencies:When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity, and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
Fosters TeamworkProvides and Solicits Honest and Actionable FeedbackSelf-AwarenessActs InclusivelyDemonstrates InitiativeEntrepreneurial MindsetContinuous LearningEmbraces ChangeResults-OrientedAnalytical Thinking/Data AnalysisFinancial ExcellenceCommunicates with Clarity
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