Senior Manager R&d Quality

2 weeks ago

Sydney, New South Wales, Australia BeiGene, Ltd. Full time

Senior Manager R&D Quality page is loaded Senior Manager R&D Quality Apply locations Sydney Australia - Home Office time type Full time posted on Posted 5 Days Ago job requisition id R23672 Bei Gene 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:

About Bei Gene:
Bei Gene (

NASDAQ:
BGNE;

HKEX:
06160;

SHA:

is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide.

With a broad portfolio of more than 40 clinical trial candidates, we are committed to expediting the development of our diverse pipeline of novel therapies through collaborations or our own internal capabilities, with the aspirational goal of radically improving access to medicines for billions more people by 2030.

Bei Gene is a headquarter-less company by design, with a growing global team of over 10,000 colleagues across five continents.


About the Position:

The Senior Manager of R&D Quality 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.


Essential Functions of the Job:

Manage and oversee R&D Quality activities which include, but are not limited to: Oversight of key QA systems such as investigations, Significant Quality Events (SQEs)/deviations, CAPAs, audits, developing and managing integrated Quality Management Risk plans Promote continuous improvement by partnering with key stakeholders to identify trends in quality events and ensure risk-based solutions are implemented in a timely manner and escalated to senior leadership Define metrics and measures for R&D Quality to drive assessment and continuous improvement Oversee GCP Quality investigations in collaboration with cross functional department owners Participate and represent R&D Quality in meetings and discussions as needed Participate in the metrics review as part of the Quality Management Risk approach to identify gaps, trends, and the need for process improvements Support the inspection readiness activities and participate in managing regulatory health authority inspections as needed Oversee Quality activities related to FDA and ROW regulations across therapeutic areas and provide GCP guidance for all phases of drug development Support routine and for cause audits of investigative sites and vendors and support internal audits Develop, review, and approve Quality - documents (e.g., SOPs).

Identify and escalate potential serious GCP non-compliances within R&D Quality management and relevant cross functional management Implement existing Quality Strategy and divisional and department-specific guidelines in all areas for which the job holder is responsible.


Qualification Required:

Additional Qualifications:

Expert knowledge of GCPs particularly ICH requirements Ability to resolve complex problems where analysis of situations or data requires an in-depth evaluation of various factors 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 Other duties as assigned

Education Required:
Bachelor's degree, preferably in

Science Supervisory Responsibilities:
This position may require mentoring of junior staff.
Therefore, it is required to have strong leadership experience and mentoring skills What we offer to our valued employees: Market competitive compensation package including performance-based annual bonus scheme Company shares (generous welcome grant and performance-based annual equity plan)

In-house and external learning and development opportunities Fantastic benefits program and keep improvingPlus you get to work with a dynamic team of collaborative, supportive, diverse, and fun professionals whose mission is clear:
Cancer has no borders and neither do we.
Bei Gene is proud to be an

Equal Opportunity Employer:
We are proud to be an equal opportunity employer and we value diversity.

Bei Gene 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.

Bei Gene 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 Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity Bei Gene 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 Bei Gene'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 Bei Gene.

For further details, please refer to Bei Gene's Job Applicant 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) Bei Gene'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) Bei Gene'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.

About Us Bei Gene 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 Bei Gene, please visit and follow us on Linked In and X (formerly known as Twitter).

To Mainland China Candidates For more information, please visit the link to explore job opportunities in China Mainland.
At Bei Gene, how we work is just as important as the work we do.
Below are our Values that determine the decisions we make and how we do things.
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