About us

BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 10,000 colleagues spans five continents, with administrative offices in Basel, Beijing, and Cambridge, U.S. To learn more about BeiGene, please visit www.beigene.com and follow us on LinkedIn and X (formerly known as Twitter).

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.

Job Description:

General Description: 

The Senior Manager/ Manager, GCP Inspection Management is responsible for implementing and maintaining a balanced, proactive, and phase appropriate approach to GCP Quality Assurance. This position will be

primarily responsible for ensuring research and development activities are conducted in accordance

with applicable regulatory requirements, guidelines, laws and internally established standards and

practices. Also responsible for the organization, planning, process and logistics of all health authority inspections.

Essential Functions of the job:

Manage and oversee the GCP Quality Assurance activities:

Conduct and/or oversee the quality assurance (QA) inspection readiness activities related to FDA and ROW regulations across therapeutic areas and provide GCP guidance for all phases of drug development

Support and manage the inspection readiness activities and participate in managing regulatory health authority inspections.

Develop/improve and manage quality systems and processes to include:

Creation/revision of appropriate SOPsImplementation and maintaining key QA systems, such as; investigations, Significant Quality Events (SQEs), Deviations, CAPAs, Audits, developing and managing integrated Quality Management Risk plans.Supporting the activities related to the vendor management process training, SOPs, etc.Supporting/managing pre-inspection visits at both investigator sites and vendors.Conducting/managing review of key documents such as study protocols, informed consent documents, Investigator brochures, Clinical study reports, submission modules, etc.Defining metrics and measures for GCP Quality Assurance to drive assessment and continuous improvementManagement and review of trends and report significant investigation/deviation issues and system deficiencies to senior management, as appropriateSupport and manage GCP Quality investigationsCoordinate and/or administer GCP training, as needed

Facilitate and manage inspection readiness meetings and represent Clinical Quality in meetings and discussions as needed

Develop a Managing Regulatory Inspections training program for the company and provide training on a periodic and as-needed basis

Participate in the review of study related metrics (i.e; protocol deviation, etc.) as part of Quality Management Risk approach to identify gaps, trends and the need for process improvements.

Promote continuous improvement

Expert knowledge of GCPs particularly FDA and ICH requirements

Ability to resolve complex problems where analysis of situations or data requires an in-depth evaluation of various factors

Ensure follow-up on all inspection commitments, responses, post-inspection activities, corrective and preventative actions, and resolve all issues for timely closure

Participate in vendor audits in accordance with BeiGene standard operation procedures, quality policies and/or plans

Create a central repository of all global/local regulatory inspection requirements and practices

Superb attention to detail, excellent review skills and the ability to organize and manage multiple tasks in a fast-paced environment.

Exercise sound and balanced judgment in ensuring that written procedures are followed and in evaluating quality systems, processes, procedures, plans and protocols for compliance

Proven ability in setting strategy for and driving quality process improvement initiatives

Strong leadership experience and mentoring skills

Strong global knowledge and understanding of international regulations applicable to the conduct of clinical trials and pharmacovigilance operations

Ensure all logistics are arranged for any Health Authority inspection (remote or on-site).

Other duties as assigned

Qualification Required:

Bachelor’s degree, preferably in Science

Communication and Interpersonal Skills

Excellent verbal and written communication skillsAbility to effectively collaborate in a dynamic environmentASQ certification is preferred

Significant Contacts

Quality AssuranceClinical OperationsPharmacovigilanceClinical Business OperationsBiometricsMedical MonitorsRegulatory AffairsInteracts with all levels of BeiGene

Travel: 

May require up to 20% travel

What We Offer To Our Valued Employees

Market competitive compensation package including performance-based annual bonus schemeCompany shares (generous welcome grant and performance-based annual equity plan!)In-house and external learning and development opportunitiesFantastic benefits program and keep improving!Plus you get to work with a dynamic team of collaborative, supportive, inclusive, and fun professionals whose mission is clear: Cancer has no borders and neither do we.Join us and Make momentum in your career!

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

BeiGene is committed to respect and protect personal information rights of job applicants and will process job applicants’ personal information in accordance with applicable laws and regulations.

Due to BeiGene’s global operation, job applicants’ data will be stored overseas with adequate protection. Besides, job applicants’ data will be stored for no longer than is necessary to facilitate potential application for other suitable positions in BeiGene. For further details, please refer to BeiGene’s Job Applicant Privacy Policy (https://www.beigene.com/privacy-policy).

If you voluntarily provide your personal information to us, it is deemed as you have acknowledged and consented to (if required by the applicable laws) BeiGene’s Job Applicant Privacy Policy as well as the relevant privacy terms. If you voluntarily provide the personal information of other job applicants to us, it is deemed as you have ensured that the relevant individuals have acknowledged and consented to (if required by the applicable laws) BeiGene’s Job Applicant Privacy Policy as well as the relevant privacy terms.

If you have any concern, please DO NOT provide any resume or other personal information to us.