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Associate Director Nucleic Acid Detection and Quantification Assays and Technologies, Walloon Brabant
Client:
1849 GlaxoSmithKline Biologicals S.A.
Location:
Job Category:
Other
EU work permit required:
Yes
Job Reference:
89c6441dcbb4
Job Views:
2
Posted:
06.03.2025
Expiry Date:
20.04.2025
Job Description:
Your responsibilities:
This role will provide you the opportunity to lead key activities to progress your career. These responsibilities include some of the following:
* Strategy, Leadership and Management: Contribute to the growth of a Global Molecular Analytics team by aligning on global priorities and portfolio management, harmonizing technical capabilities, development approaches, documentation, resource constraints, and appropriate risk-taking. Define a phase-appropriate strategy for the development and implementation of testing methods for candidate vaccines covering the early and late phase development and product launch. Identify risks related to process feasibility, manufacturability, timing, and resource constraints and develop remediation plans. Escalate any technical issues to the Technical Development Team. Lead and manage a team of scientists and researchers, fostering a collaborative and innovative work environment. Provide strategic direction and oversight for nucleic acid detection and quantification projects. Mentor and develop team members, ensuring continuous improvement and professional growth. Perform a leadership role for safety, regulatory, compliance or data integrity on behalf of GSK.
* Research and Development: Drive the development, validation, and optimization of nucleic acid detection and quantification assays and technologies based on QbD principles. Oversee the design and execution of experiments, ensuring robust and reproducible results. Collaborate with cross-functional teams to integrate new technologies and methodologies into ongoing projects. Influence project priorities, manage the local portfolio, and encourage smart risk-taking to accelerate vaccine development.
* Quality Control and Compliance: Implement and maintain stringent quality control measures across all stages of assay development and deployment. Ensure compliance with industry standards, regulatory requirements, and company policies. Conduct regular audits and reviews to identify areas for improvement and implement corrective actions.
* Project Management: Manage multiple projects simultaneously, ensuring timely completion and alignment with company goals. Develop project plans, allocate resources, and track progress against milestones and deliverables. Communicate project status, challenges, and outcomes to senior management and stakeholders.
* Innovation and Continuous Improvement: Stay abreast of the latest advancements in nucleic acid detection and quantification technologies. Identify and evaluate emerging trends and technologies for potential integration into the company’s portfolio. Foster a culture of innovation and continuous improvement within the team.
Basic Qualifications:
* PhD degree (biotechnology, molecular biology, biochemistry, (molecular) bacteriology, (molecular) microbiology, etc.) with more than 5 years of experience in the industry (in biologics / biopharmaceuticals / pharmaceutics) or equivalent by experience.
* Proven knowledge of NAT analytical methods relevant to the role and proven application of said methods preferably to vaccine and/or biological products (viruses, bacteria, recombinant cell lines, RNA, DNA, and plasmids).
* Experience/knowledge about method transfer to QC, answers to Regulatory Agencies questions, use of NAT data for file submissions.
* Languages: fluent in French and English (spoken and written). Fluent English knowledge is a must.
* Good organizational skills.
* Teamwork and efficient interaction with line management and other Associate Directors.
* People management, coaching, communication, innovation orientation, synthesis and analytical capacity, presentation skills, influencing, flexibility.
Preferred Qualifications:
* A strong background in molecular microbiology.
* Expert knowledge in QPCR assays, direct nucleic acid detection techniques, nucleic acid separation by different electrophoresis techniques, molecular cell biology, microbiology.
* Ability to work within a diversity of cultures and teams located in different time zones.
* Good understanding of Computerized-System Validation, ALCOA-CCEA principles, and GMP requirements.
* Demonstrate communication skills with external key opinion leaders/experts in specific therapeutic areas or scientific disciplines.
* Demonstrate good judgment and effective decision making in applying expertise to move multiple scientific or technical projects forward.
If you have a disability and require assistance during the selection process, you will have the opportunity to let us know what specific assistance you require.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together. Our success absolutely depends on our people. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
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