Qc Manager Cgt

Vor 3 Tagen

Stein, Schweiz Novartis Vollzeit

25000+ The total no. of associates in NTO who deliver high quality, affordable medicines on time, every time, safely and efficiently. We strive to become the top manufacturer of innovative and generic medicines in the industry - while keeping our patients at the heart of everything we do.
- Major accountabilities:
- Manages laboratory personnel, provides feedback (formal and informal) and mentoring to team members on routine basis, execute performance appraisals for direct reports and ensures proper training status of personnel.
- Supervises QC activities and priorities to meet the timelines and ensures operational continuity, conducts additional projects or other specific assigned tasks independently or with mínimal supervision and drives for efficiency whenever possible.
- Ensures that all activities, including equipment and reagents utilization, are in compliance with current Good Manufacturing Practices, with Health, Safety and Environmental policies, the global/local Novartis policies and procedures, the regulatory guidelines, and industry standards.
- Leads method validation/transfer activities (incl. writing of protocols and reports).
- Writes and review SOP’s, testing procedures, protocols and reports.
- Evaluates/troubleshoots routine and non-routine technical and analytical problems and leads laboratory and cross functional investigations to identify the root causes and implement appropriate corrective actions in a timely manner.
- Participate in audits (internal / external) where necessary (prep, support, interactions) and supports following up and concluding resulting actions.
- Participates in the preparation and consolidation of the budget of the Quality Control Unit and contributes to site QC strategy

**Commitment to Diversity & Inclusion**:

- Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._

**Minimum requirements**
- MS in biology, chemistry, biochemistry, microbiology or other related science.
- Fluency in English language
- Minimum of 8 years of experience in the Pharmaceutical/Biotechnology industries conducting QC testing, release testing and coordinating the activities of a QC laboratory.
- Previous people management experience.
- Knowledge of cGMP, USP and FDA guidelines.

Join our Novartis Network:

Why Novartis?
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
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’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying
Imagine what you could do here at Novartis

**Division**
- Novartis Technical Operations

**Business Unit**
- QUALITY

**Country**
- Switzerland

**Work Location**
- Stein (Säckingen)

**Company/Legal Entity**
- Novartis Pharma AG

**Functional Area**
- Quality

**Job Type**
- Full Time

**Employment Type**
- Regular

**Shift Work**
- No

**Early Talent**
- No

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