We are looking for a Junior Global Supply Planner for our biotech client in Breda.
You work on ensuring supplies for clinical studies that run globally and mostly under the supervision of an experienced planner. You will be working on the largest and fastest lane trials. After training and proven experience, you will be working independently on less complex studies. The planning team works to reach a minimum of 99,99% for patient dosing with decision making on the right inventory levels at central warehouses and hospitals. During the entire length of the clinical trial, the study planner is responsible for updating the demand for the global patient portfolio for the assigned studies and monitoring supply at all locations to minimize product waste.
Responsibilities
- Propose to translate study team requirements into an actionable global supply plan
- Help with detailing forecasting demand and demand patterns, including key stakeholder meetings, to ensure the adequacy of supply/re-supply strategies. Where necessary, and actively participate in planning meetings to ensure that project needs, priorities, and timing are understood
- Serve as the secondary interface with clinical study team, Quality, and Regulatory Affairs to ensure coordination of all activities necessary to maintain the forecast and ensure an adequate supply plan
- Resolve logistical conflicts impacting studies and R&D milestones, ensuring that supplies are not on the critical path
- Coordinate labeling, packaging, and shipment of labeled supplies
- Promptly identify and escalate risks to study timelines or clinical supplies, from a supply chain perspective, to all key stakeholders and internal management
- Utilize systems to effectively manage key product/project activities
- Help understand clinical supply chain management processes and strategies to key stakeholders
- Review and update existing procedures and SOPs; identify the need for and assist in the establishment of new procedures and SOPs
Qualifications
Minimum Requirements
- Bachelor’s degree in supply chain or business administration and 6 months of relevant working experience
- Fluency in English, both in verbal and written communication
- Fluency in Dutch is preferred
Preferred Requirements
- Experience of working in a fast-paced complex supply chain environment
- Experience in MS Office applications
- Experience in Digitization
- Experience in using ERP systems, preferably SAP
- Experience with AI tools
What We Offer:
- A hybrid working model in a dynamic and growing biotech company
- An attractive salary package with extra benefits
- 13th-month bonus and holiday allowance
- An opportunity to work in an international, regulated environment with career development opportunities
Interested?
Send your CV to b.didomenico@panda-int.com today! Let’s connect promptly.
Know someone who might be a good fit? Feel free to introduce us!
Refer a friend and earn €250 for successful referrals.
We are looking for a Junior Global Supply Planner for our biotech client in Breda.
You work on ensuring supplies for clinical studies that run globally and mostly under the supervision of an experienced planner. You will be working on the largest and fastest lane trials. After training and proven experience, you will be working independently on less complex studies. The planning team works to reach a minimum of 99,99% for patient dosing with decision making on the right inventory levels at central warehouses and hospitals. During the entire length of the clinical trial, the study planner is responsible for updating the demand for the global patient portfolio for the assigned studies and monitoring supply at all locations to minimize product waste.
Responsibilities
- Propose to translate study team requirements into an actionable global supply plan
- Help with detailing forecasting demand and demand patterns, including key stakeholder meetings, to ensure the adequacy of supply/re-supply strategies. Where necessary, and actively participate in planning meetings to ensure that project needs, priorities, and timing are understood
- Serve as the secondary interface with clinical study team, Quality, and Regulatory Affairs to ensure coordination of all activities necessary to maintain the forecast and ensure an adequate supply plan
- Resolve logistical conflicts impacting studies and R&D milestones, ensuring that supplies are not on the critical path
- Coordinate labeling, packaging, and shipment of labeled supplies
- Promptly identify and escalate risks to study timelines or clinical supplies, from a supply chain perspective, to all key stakeholders and internal management
- Utilize systems to effectively manage key product/project activities
- Help understand clinical supply chain management processes and strategies to key stakeholders
- Review and update existing procedures and SOPs; identify the need for and assist in the establishment of new procedures and SOPs
Qualifications
Minimum Requirements
- Bachelor’s degree in supply chain or business administration and 6 months of relevant working experience
- Fluency in English, both in verbal and written communication
- Fluency in Dutch is preferred
Preferred Requirements
- Experience of working in a fast-paced complex supply chain environment
- Experience in MS Office applications
- Experience in Digitization
- Experience in using ERP systems, preferably SAP
- Experience with AI tools
What We Offer:
- A hybrid working model in a dynamic and growing biotech company
- An attractive salary package with extra benefits
- 13th-month bonus and holiday allowance
- An opportunity to work in an international, regulated environment with career development opportunities
Interested?
Send your CV to b.didomenico@panda-int.com today! Let’s connect promptly.
Know someone who might be a good fit? Feel free to introduce us!
Refer a friend and earn €250 for successful referrals.