[Company / Industry] Global healthcare logistics company / Supply and Logistics
[Position] Depot Manager
[Function] Operations and support
[Reporting Line] Senior Manager, Depot OPS APAC
[Employment Type] Permanent
[Compensation] TBD
[Location] Seoul, Korea
[Consultant in charge] Simon S. Kim
Company Description:
Reputable global company specializing in logistics for clinical trial materials and sensitive drug shipments.
Job Description
[Depot Set-Up]
Responsible of the setting up Depot in the Country ensuring that the facility will be compliant with the GMP national and international guidelines.
Implement operational processes according to the Company QMS and Global SOPs
Implementation of the administrative processes that support the functionality of the Depot.
Recruitment and training processes.
Ensure that the commissioning and preparations over the Facility are in place for the execution of validation processes in the Depot.
Execute within the contracted Validation Company the Qualification plan of the depot
Assist in the required Licensing submission process according with the Country regulation.
[Depot Management]
Manage the internal Depot operations according to SOPs to ensure service levels are met.
Implement plans for the facility including staffing levels, operations to meet client and business requirements.
Support QA function to ensure compliance with GMP.
Develop business opportunities.
[Others]
Develop operational SOPs associated with local procedures.
Assisting the sales team in provision of information pertinent to the regional capabilities.
[General]
Manage the internal Depot facility operations to ensure service levels are met
Ensure compliance with national and international standards and legislation
Travel as reasonably requested by the Line Manager for the performance of duties
Development of the Depot and assist in the development of the Depot storage and distribution network within the Company
Undertake any other reasonable duties at the request of the Line Manager
To adhere to all company Policies at all times
Job Requirements
Comprehensive knowledge of Good Manufacturing Practice guidelines
Comprehensive knowledge of local Clinical Trials Regulations within the Country
Knowledge of cold chain supplies and logistics
Excellent written and oral communication skills
Good interpersonal skills
Organized, methodical and efficient approach to work
Proficient use of Microsoft applications.
Fluent in English / Native Korean
A minimum 5 years experience working in a CTS environment with knowledge of the Clinical Trials supply chain.
Line Management experience
Bachelor degree level.
Academic background of careers related to Pharmacy, Logistics, International Commerce, Health Science and Supply Chain
If you are interested, please contact simon.kim@rp4rp.com +82-10-4118-2178