Leads a team to execute project work for the development of the Global Swine Biologicals portfolio that is related to China.
In this capacity PL manages tasks, outstanding issues, obstacles or barriers, and deadlines for one or several projects, and reports progress and deviations to senior management on a regular base.
Escalates issues in resources or other limitations to management in a timely fashion.
Ensures information flow between the individual disciplines required to perform the activities.
Ensures that work is carried out with scientific integrity and according to the existing internal guidelines for EHS and compliance.
Can be asked to advise and help out local regulatory affairs on regulatory matters.
Act as a generalist with interdisciplinary competence and experience.
Acts as direct manager for (Associate) Scientists.
Performs project related literature searches. As required publishes and present technical papers to internal and external audiences, (co-)author of scientific publications.
May initiate, plan and execute external research cooperation's and cultivate relationships with external stakeholders.
Function as study director for clinical studies and may act as principle investigator or study director for multisite (GLP/GCP) studies after appropriate training.
May organize and plan animal experiments and is responsible for staying informed and acting according to the local laws on animal experimentation.
Plans stock of biomaterial (e.g. antigens and vaccines) for use in development.
Involved in review of production process, scale-up, validation, control test, lab study and field study reports.
Responsible for directing development and validation of laboratory methods and techniques.
Implements and maintains relevant report systems and uses a software program that host all project plans and their countable/measurable information.
Responsible for developing a project plan that works to achieve progression criteria using sound technical and scientific processes in the shortest amount of time with the least cost.
Is open for general tasks within the organization related to GLP, EHS IT and/or laboratory coordination.
Fluent English communication and writing.
MNCs experiences 5yrs+ or the equivalent experiences in AH vaccine indurstry.
Familiar with CN regulation for AH Bio registration.
PhD are preferable.
Regular Employee Status.
Domestic Relocation.
No VISA Sponsorship.
10% Travel Requirements.
Not Applicable Flexible Work Arrangements.
Not Indicated Shift.
No Valid Driving License.
n/a Hazardous Material(s).
Required Skills: Applied Engineering, Assay Development, Biochemical Assays, Biochemistry, Bioinformatics, Business, Cell Biology, Detail-Oriented, Development Projects, Ethical Compliance, High-Throughput Screening, Immunology, Job Descriptions, Laboratory Analysis, Laboratory Techniques, Literature Searches, Mammalian Cell Culture, Management Process, Molecular Biology, Production Operations, Production Processes, Professional Networking, Project Development, Project Planning.
Preferred Skills:
Job Posting End Date: 09/30/2025.
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Tagged as: Life Sciences
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