Supply Chain Manager - Pharmaceutical - Drug Development

Hiring LGBT+ TALENT (LGBT+ stands for Lesbian, Gays, Bisexual, Transgender)

Job Title: Supply Chain Manager - Pharmaceutical (Drug Development)

Location: Hyderbad

Company: Big Pharmaceutical Client

CTC: Best in the Industry

Experience: 10 to 12 years

Job Description:

Join a team of globally collaborative colleagues at the - Global Clinical Supply (GCS)- function to support clinical trials from Phase 1 to approval and be a key interface between Technical Research & Development teams and the Clinical teams!

The Supply Chain Manager (SCM) is responsible for Demand and Supply Planning from Clinical Finished Good (CFG) to Drug Substance (DS) ensuring demand fulfillment for assigned projects. The SCM acts

as key contributor to the Clinical Supply & Operations Planning (CS&OP) process in TRD/BTDM/GCS and provides transparency on supply constraints and manages related aspects accordingly within TRD and BTDM.

Execute and monitor timely activities related to assigned area of responsibility under the guidance and accountability of more senior associates.

YOUR KEY RESPONSIBILITIES:

- Creates and maintains the end-to-end supply plan from CFG to DS. Harmonizes the supply strategy within GCS and contributes to the supply strategy of CHAD/PHAD/ BTDM.

- Leads the Clinical Demand Planning Meeting (CDPM) ensuring alignment between demand and supply.

- Ensures demand fulfillment and coverage of supply and regulatory aspects by contributing to GCS agenda at TRD Sub team/BTDM CMC meeting. Represent GCS at TRD Sub team/BTDM CMC on supply chain aspects.

- Optimizes the inventory strategy at PP and CFG level together with CTSM. Actively contributes to the portfolio manufacturing schedule alignment (from DS to CFG). Defines most cost-efficient ordering levels from CFG to DS, minimizing waste and allowing flexibility to accommodate demand variability.

- Supports Long-term demand and capacity planning (LTDCP). Adheres to SCM KPI for project and unit. Manages ordering activities and master data requirements in SAP within the scope of the role

- Drives the comparator sourcing activities and comparator blinding strategy. And also Oversees Comparator resupply strategy in support of budget planning

- Provides impact assessment on clinical supplies and contribute to the regulatory submission strategy

- Engages and contributes to the Clinical Packaging Execution Meeting (CPEM) to ensure alignment with Operations and Supply continuity.

Minimum requirements:

- 10 years of practical experience in chemical / pharmaceutical industry or > 5 years of experience in field of expertise

- Good knowledge about the Drug Development process.

- Basic project management, good organization and planning skills

- Good knowledge of HSE/GMP standards and processes

- Problem-solving and idea generation skills

- Good presentation skills, Fundamental Leadership skills.

- Good communication, negotiation and interpersonal.

If you belong to the LGBT+ community then please send your CV

NOTE: We are only considering applications from LGBT+ candidates (LGBT + stands for Lesbian, Gays, Bisexual, Transgender, Queer, Intersex)