Job Overview
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Date PostedAugust 4, 2023
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Location (State / UT)
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Expiration date--
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Experience3 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
Women Candidates Preferred
Roles and Responsibilities
- Contribute to the completion of projects and manage own time to meet agreed targets and develop plans for activities on own projects.
- Develop inventory targets and budgets.
- Consult with and informs AMP Supply Planners of market dynamics that influence continuity of supply, both through forecast adjustments as well as through dialogue when appropriate.
- Responsible for ensuring Supply Assurance and Supply Chain performance of an assigned portfolio of products.
- Represent region in global and regional forums (for assigned product portfolio).
- Monitor and manage inventory shelf-life and expiry dates minimizing write-offs whilst improving processes to avoid obsolescence.
- Plan and implement routine launches, in-line product extensions, and major product changes enabling business unit growth.
- Perform root cause analysis of inventory deviations vs. targets and of inventory drivers and define improvement plans.
- Partner with AMP Team Lead and AMP Hub Senior Supply Planners to drive resolution of escalated issues in SCA (Supply Chain Agreement).
- Exhibit strong knowledge of legislation, market practice, and understanding of the local Logistics market business environment.
- Serve as point of contact to brand supply leads and manufacturing sites for any questions related to supply issues, resolution plans, and inventory for assigned sets of products.
- Manage market forecasts in partnership with Supply Chain and related Pfizer Global Supply colleagues and functions.
- Ensure compliance with all relevant regulations and a state of audit readiness.
- Collect the data, Evaluate the assessed notification with impacted functions above site with respect to Quality, Supply risk, Regulatory & Product Impact
- Acquire the process knowledge and lead the change implementation in coordination with the functional teams.
- Ability to liaise with cross functions for impact assessment and adherence to the committed timelines.
- Change request management, initiation, tracking the impact assessment, Pre-approval, and closure of change on time.
- Ensuring resolution of the identified issues and providing timely implementation of each project
- Maintain a consistent supply of our products to the market, while maintaining compliance to cGMPs.
- Authorize the impacted procedures for the change and connect with cross functions for the necessary detail
- Review the provided impact from the associated function and document within the change request
- Prepare the quality risk assessment documents depending on the type of change
- Coordinate with cross-functional teams such as Pfizer site operations, Supply chain, Procurement, Engineering, Regulatory Affairs, Validation, and Quality Assurance teams for smooth execution of the project.
- Maintain/establish a governance process for the management of SCNs from initiation to implementation
- Ability to pitch in & work on an ad-hoc basis wherein a supply risk is posed and act prompt
- Work and own the process to identify any cost-improvement projects
- Ability to work up, down, across the organizations supporting the centralization team needs
- Support the central teams as needed with respect to investigations related to SCNs
Qualification:
Must-Have
- Bachelor’s Degree
- 3+ years experience
- Experience and working knowledge of Clinical Supply Systems
- Demonstrated experience in pharmaceutical operations, understanding of pharmaceutical industry commercial dynamics, trends, and regulatory processes.
- Knowledge of production and capacity planning, shop floor control, distribution planning, and inventory control
- Ability to observe patterns and trends in data, determine root cause of issues and draw proper conclusions from the analysis
- Develop effective relationships with multiple stakeholders and a quick grasp and understanding of complex situations involving many moving parts
- Fluent in both written and verbal English
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Nice-to-Have:
- Master’s degree
- Knowledge and experience in System Application & Products environment