Job Description

Job Description ​

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.

Competencies

Fluent English communication and writingMNCs experiences 5yrs+ or the equivalent experiences in AH vaccine indurstryFamiliar with CN regulation for AH Bio registrationPhD are preferrable

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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

Applied Engineering, 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 {+ 5 more}

 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.

Requisition ID:R355923