Senior Clinical Supply Chain Coordinator
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Biotechnology organisation, based in Noord-Brabant Netherlands.
• Provide extensive backup to other functions in the CCS team
• Responsible for one or more subject matter expert areas
• Manage assigned controlled documents and quality records (CTETS, NC class 1/ CAPA)
• Responsible for maintenance and reporting of a assigned set of metrics
• 1st point of contact for site issue resolution
• Independently resolve tier 1 issues (distribution related)
Sales Order management:
• Create and Process Clinical Drug Shipments
• Create or coordinate obtaining of necessary shipping documentation
• Resolve drug shipment issues
• Track and trace shipments
Stock Transfer Order Management:
• Schedule and Process STOs
• Create or coordinate obtaining of necessary shipping documentation
• Track and trace shipments and ensure smooth delivery to LSP
• Resolve shipping issues
Manual and Electronic Proof of Receipt (POR):
• Handle and record receipt of POR
• Resolve POR/ EPOR issues, including handling of CTETS records
Temperature data review:
• Perform review of temperature data for shipments with specific temperature requirements
• Create and own CTETS records
• Coordinate product release with the QA department
• Manage changes of IVRS status
• Support performance of data analysis, trending and corrective actions
Management of site temperature excursions:
• Enter incoming site TEs into CTETS and perform assessment
• Manage changes of IVRS status
• Coordinate TE review with QA
• Coordinate communication with the site (monitors)
Returns and reconciliation:
• Close out returns in SAP and support reconciliation campaigns as needed
• Archiving of return documentation
Additional responsibilities (as applicable locally):
• Manage import licenses and import/ export requirements per country as applicable
• Support expiry relabeling campaigns
• Manage destruction of returned/ cancelled orders
• Intake of clinical complaints and coordinate return of complaint samples
• Execute upload to of LSP data into SAP
• Execute shipments of packaging materials to the LSPs
• Archiving
• Fluency in English, both in oral and written communication.
• Strong computer skills, experience in working with automated systems (computer based business systems) like MS-Office, preferably with SAP
• Good Excel skill
• Experience in working with projects
• Results oriented, strong adherence to timelines.
• Accurate and attention to detail.
• Process-oriented.
• Excellent communication skills (both written and verbal).
• Ability to interface effectively at all levels with international peers and departments.
• Applies experience and judgment to make decisions or resolve issues within or outside defined options or standard protocols
• Anticipated problems and recognizes when to deviate from the standard practices
• Ability to improve processes
• Sets priorities within general guidelines
• Ability to operate in a team and strongly-matrixed environment
• Ability to handle multiple responsibilities and priorities simultaneously in a fluid environment with time pressures
• Diplomacy
• Persuasion
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ravi Ramnarain Singh.
The Company
.Role Description
• Provide distribution support to the planning and LSP teams• Provide extensive backup to other functions in the CCS team
• Responsible for one or more subject matter expert areas
• Manage assigned controlled documents and quality records (CTETS, NC class 1/ CAPA)
• Responsible for maintenance and reporting of a assigned set of metrics
Responsibilities
Issue resolution:• 1st point of contact for site issue resolution
• Independently resolve tier 1 issues (distribution related)
Sales Order management:
• Create and Process Clinical Drug Shipments
• Create or coordinate obtaining of necessary shipping documentation
• Resolve drug shipment issues
• Track and trace shipments
Stock Transfer Order Management:
• Schedule and Process STOs
• Create or coordinate obtaining of necessary shipping documentation
• Track and trace shipments and ensure smooth delivery to LSP
• Resolve shipping issues
Manual and Electronic Proof of Receipt (POR):
• Handle and record receipt of POR
• Resolve POR/ EPOR issues, including handling of CTETS records
Temperature data review:
• Perform review of temperature data for shipments with specific temperature requirements
• Create and own CTETS records
• Coordinate product release with the QA department
• Manage changes of IVRS status
• Support performance of data analysis, trending and corrective actions
Management of site temperature excursions:
• Enter incoming site TEs into CTETS and perform assessment
• Manage changes of IVRS status
• Coordinate TE review with QA
• Coordinate communication with the site (monitors)
Returns and reconciliation:
• Close out returns in SAP and support reconciliation campaigns as needed
• Archiving of return documentation
Additional responsibilities (as applicable locally):
• Manage import licenses and import/ export requirements per country as applicable
• Support expiry relabeling campaigns
• Manage destruction of returned/ cancelled orders
• Intake of clinical complaints and coordinate return of complaint samples
• Execute upload to of LSP data into SAP
• Execute shipments of packaging materials to the LSPs
• Archiving
Requirements
• HBO education + 2-3 years relevant working experience/ MBO + 5 years relevant working experience/ Bachelor’s degree +2 years of supply chain experience/Associate’s degree + 6 years of SC experience/ High School Diploma/ GED + 8 years of SA experience/ Master’s degree + no SC experience• Fluency in English, both in oral and written communication.
• Strong computer skills, experience in working with automated systems (computer based business systems) like MS-Office, preferably with SAP
• Good Excel skill
• Experience in working with projects
Other information
Competencies• Results oriented, strong adherence to timelines.
• Accurate and attention to detail.
• Process-oriented.
• Excellent communication skills (both written and verbal).
• Ability to interface effectively at all levels with international peers and departments.
• Applies experience and judgment to make decisions or resolve issues within or outside defined options or standard protocols
• Anticipated problems and recognizes when to deviate from the standard practices
• Ability to improve processes
• Sets priorities within general guidelines
• Ability to operate in a team and strongly-matrixed environment
• Ability to handle multiple responsibilities and priorities simultaneously in a fluid environment with time pressures
• Diplomacy
• Persuasion
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ravi Ramnarain Singh.
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