Job Description

2023 will potentially see Sandoz become a standalone organization! Already a global market leader in Generics and Biosimilar medicine, this is an exciting, once-in-a-career opportunity to set our own path forward as an independent, purpose-driven organization, and as the founders of a new Sandoz, this is a time of immense opportunity for us all, both professionally and personally!

Together we will shape the future of Sandoz\xe2\x80\xa6 are you ready to make a difference?

Position Purpose:
Responsible for the site Master Data processes striven to ensure accurate and timely creation and maintenance of the master data in the ERP System, in accordance with local and global requirements. The Material Planner drives the tactical purchasing process for all materials to ensure materials availability and execution plan feasibility in accordance with Site inventory policy.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum requirements
Your Key Responsibilities:
Your responsibilities include, but not limited to:

• Ensures, defines and governs consistent master data throughout the whole master data life cycle and global business processes and defines the matrix of responsibilities within the MD process and the person that defines the parameter, the person who updates SAP with the right value, etc.
• Ensures that local material master data integrity and quality is established by analyzing basic requirements, maintaining the attributes in the systems and assuring all data introduced in the system is reliable and comes from the accurate sources and challenges data consistency and completeness and verifies, accurate and completes requests for data maintenance aligning with Global Master Data processes and related SOPs.
• Identifies areas for improvement regarding Global Material Master processes, tools and rules and supports improvement processes. Responsible for specific Master Data Management processes (expertise, key account) to build, extend and share knowledge within self-directed working teams.
• Train and support the assigned functional SPoCs and Domain Experts on site and ensure compliance with GMP and regulatory requirements (including record management) and continuous improvement of quality relevant processes within area of responsibility. Ensures permanent data quality and assists in data base cleaning. Ensure material availability in line with the approved production plan.
• Ensure daily MRP oversight for all BOM material, analysis of requirements and Purchase Orders management. Ensure management of daily MRP exception messages & appropriate follow up. Own, in ERP System, MRP relevant data and materials technical specifications and ensure no Purchase Orders are past due in the ERP System.
• Management of purchased item Complaints/Returns to supplier. Provide a load balanced dispatch list for incoming materials to the warehouse and Quality department that ensures these activities are completed in line with the production needs.
• Control and follow-up of supplier\xe2\x80\x99s service level indicators: Quality OTIF, lead-time Violation. Lead action plans to achieve supplier delivery performance targets and drive for continuous improvement.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt, Distribution of marketing samples (where applicable).

What you\xe2\x80\x99ll bring to the role:
Essential Requirements:

• Graduate / Post Graduation especially with a supply chain background Certification in supply chain will be added advantage with min 4+ yrs exp.
• Ability to work successfully with extended, multinational project teams and coordinate activities simultaneously on multiple projects under pressure of time and workload
• Effective planning, organizational and interpersonal skills
• Reasonable approach to risk assessment
• Excellent written/spoken communication and negotiation skills.
• Ability to work independently without much handholding & guidance.

Commitment to Diversity & Inclusion:
Sandoz is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Why Sandoz?
453 million patients were touched by Sandoz generic and biosimilar medicines in 2022 and while we\xe2\x80\x99re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world.

How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what\'s possible, when we collaborate with courage to aggressively and ambitiously tackle the world\xe2\x80\x99s toughest medical challenges. Becau
Division
SANDOZ
Business Unit
Global Functions STO
Country
India
Work Location
Hyderabad, AP
Company/Legal Entity
Sdz Pvt Ind
Functional Area
Technical Operations
Job Type
Full Time
Employment Type
Regular
Shift Work
No
Early Talent
No