QA Operations Expert

vor 2 Wochen

Stein, Schweiz Novartis Vollzeit

Novartis Technical Operations (NTO) brings billions of
units of medicine to countries around the world. Our mission is to ensure the delivery of high quality products to patients around the globe.
As a QA Operations Expert you will be responsible for managing quality aspects within area of responsibility and to ensure that the operational business is in compliance with cGMP (Current Good Manufacturing Practices), the Quality Assurance Agreement, regulatory requirements & the Novartis Quality Manual and is conducted according to the relevant Standard Operating Procedures.

**Your key responsibilities**:

- Oversight of all production & testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance
- Executes Batch Record review and technical Batch Release in compliance with registration Support exception investigations
- Support exception Investigations and local/global Escalations
- Support OpEx improvement projects if applicable
- Proven profound knowledge in aseptic/sterile manufacturing, Quality Assurance or any other Quality Department, e.g. Compliance or Quality Control.
- Proven working under flexible conditions and changing priorities/ handling time critical tasks
- Proven responsibility of decision taking and leading multiple tasks as a QA SPOC
- Working as a contributor with all stakeholders, e.g. Manufacturing Unit, Supply Chain, other QA groups, QC

**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**

**What you’ll bring to the role**:

- 3-5 years professional experience in GMP environment and/or analytics (e.g., Quality Control, QA Compliance)
- Fluent in German and English (written and verbal communication)
- Bsc./Msc or Phd. of Science in Pharmacology, Pharmaceutical Sciences, Chemistry, Microbiology or technical science background, e.g. engineer in Biotechnology/Pharmatechnology

**Desirable requirements**:

- 5+ years experience in Quality department or equivalent Manufacturing position in the pharmaceutical industry

**You’ll receive**:
Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, Unlimited learning and development opportunities.

**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**

**Commitment to Diversity & Inclusion**
Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve.

**Accessibility and accommodation**

**Division**

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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