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.

Note: To be considered for our 2025 Summer Internship program you must be enrolled in a university degree program and cannot be graduating sooner than December 2025. 

Education Required:

Actively enrolled in a university program (not new grads). Undergraduate, Graduate/Masters and PhD/PharmD programs.Familiarity with clinical trial processes and GCP is a plus.

General Description/Scope of Responsibilities (Internship): As an intern in the R&D Quality GCP (Good Clinical Practice) Audit function, you will support the team in ensuring compliance with GCP guidelines and regulatory requirements.

Essential Functions of Job:

Your tasks may include:

Assisting in uploading, organizing, and maintaining audit-related documents in Veeva Vault QualityAssisting in the management of auditor qualification and training records and ensuring proper document version control.Assisting in updating and maintaining the annual GCP audit plan including providing support to ensure audit schedules, audit scopes, and assigned auditors are accurately recorded (using Excel or Project).Assisting in streamlining the process to prepare, schedule, and coordinate GCP audits.Supporting document review and organization related to GCP audits.Participating in meetings and taking minutes as needed.Collaborating with cross-functional teams to support quality and compliance initiatives.

This role will provide you with hands-on experience in clinical quality assurance, regulatory compliance, and audit processes in a biotech environment.

Skills and Knowledge:

Basic understanding of GCP (Good Clinical Practice) and regulatory compliance within the pharmaceutical or biotech industry.Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint) for tracking, reporting, and presentation creation.Familiarity with Veeva Vault or other document management systems is preferred but not required.Strong attention to detail and organizational skills for maintaining audit records and tracking plans.Good communication skills to coordinate with different teams and stakeholders.Analytical mindset for data management and report generation.

Personal Qualities:

Eagerness to learn and contribute to the quality and audit processes.Ability to work independently as well as collaboratively in a team setting.Proactive approach to problem-solving and a passion for improving processes.Strong time management skills and ability to prioritize tasks effectively.

Preferred Experience (not mandatory):

Any prior internship experience in Quality Assurance, Regulatory Affairs, or Clinical Research.Knowledge of CAPA (Corrective and Preventive Actions) and Audit Management processes.

This internship will help you gain hands-on experience in audit planning, document management, and compliance monitoring within the context of clinical trials and regulatory standards.

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

We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.