External Operations Manager
vor 4 Wochen
**Summary**:
**About the Role**:
**Key Responsibilities**:
- Acts as the key business partner for operational interactions with the Vendors. Reviews the vendor capacity, resource planning and distribution tracker and verifies this with the study requirements to ensure the study timelines and specifications are met.
- Manages deviations occurring at external vendors and escalates high level issues/bottlenecks to the relevant internal GCS stakeholders and external partners and other compliance related tasks involved with maintaining qualification status of the vendor
- Liaises with Comparator Sourcing Supply Lead and internal GCS study team (with Clinical Trial Supply Manager and Comparator Sourcing Supply Lead) on a regular basis to create orders based on the project specific requirements.
+ ensure operational responsiveness to study dynamics.
- Ensures most cost-efficient material flow, minimizing waste and allowing the flexibility to accommodate the changing demand.
- Participates or supports external inspections and audits together with Technical Research & Development (TRD) QA (and Good Clinical Practice (GCP) QA where applicable) to assess contractor capabilities.
- Being sub-process owner in GCS, drives innovation in the areas of process simplification and cost reduction.
- Contributes to productivity targets by continuously improve processes in own area of expertise.
- Liaises with GCS counterparts to review project status.
- Monitors vendor performance with pre-defined KPIs and collaborates with vendor to identify process optimizations and ensures timely follow up and completion of actions.
**Essential Requirements**:
- Degree in science, engineering or equivalent.
- >5 years of practical experience in chemical / pharmaceutical industry or > 3 years of experience in field of expertise
- Good knowledge about the Drug Development process
- Basic project management, good organization and planning skills
- Knowledge of Good Manufacturing Practices and Health, Safety & Environment (GMP & HSE) regulations.
- Very good communication, Fundamental Leadership, negotiation and interpersonal skills and the ability to work in interdisciplinary teams.
**Desirable Requirements**:
- Degree in Science
- Distribution experience in Pharma
In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group. Level 4: In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is €60,212.18/year (on a full-time basis). The actual salary will be significantly higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies.
**Commitment to Diversity and Inclusion**:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Division
Development
Business Unit
Pharmaceuticals
Location
Austria
Site
Schaftenau
Company / Legal Entity
AT33 (FCRS = AT033) Novartis Pharmaceutical Manufacturing GmbH
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
**Adjustments for Applicants with Disabilities**:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
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