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Expert Science & Technology (mfd)
Expert Science & Technology (mfd)Novartis • Basel, Basel-Stadt, Switzerland
Expert Science & Technology (mfd)

Expert Science & Technology (mfd)

Novartis • Basel, Basel-Stadt, Switzerland
Il y a plus de 30 jours
Description de poste

Job Description Summary

Location : Basel Switzerland #onsite

Role Purpose :

We are looking for a highly motivated Expert in Science & Technology to support Analytical Research & Development (ARD). ARD sits within the Global Technical R&D department of Development and plays an essential role in the characterization and analysis of Small Molecule Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. The role will be part of the Small Molecules GMP Analytics Team with focus on small molecules and Radioligand Therapy.

Job Description

Major accountabilities :

Independently plan organize execute and document scientific experiments (e.g. stability / release testing validations etc.) according to the agreed timelines and appropriate quality standards.

Execute experiments using state of the art analytical instruments e.g. HPLC

Perform Cleaning validation / verification experiments

Accountable for documentation and submission of raw data in appropriate data system (e.g. GLIMS eLN ).

Responsible for good documentation practices (GDP) and good laboratory practices (GLP) during execution of laboratory activities.

Responsible for assigned laboratory related area / activities (e.g. chemical / reagents / consumables / samples / column / glassware management etc.).

Support in evaluation and interpretation of results including investigations on SST failures OOX / Deviations / Change controls as needed.

Support management of TRD planning tool (PLATON)

Train and coach associate scientists technicians temporary employees and employees under training / education

Proactively communicate key issues and any other critical topics in a timely manner to the manager and / or to any other relevant project team member(s).

Responsible to meet KQI (Key quality indicators) and KPI (Key performance indicators) for all assigned activities.

Work according to appropriate SOPs GMP HSE ISRM and Novartis Guidelines

Minimum Requirements :

Bachelors / Masters in Life Science (e.g. analytical / organic chemistry / pharmacy / pharmaceutical development) or equivalent

3 years of related experience in a GMP environment

Experience with HPLC Cleaning validation / verification

Experience working with eLN

Experience working with digital tools VBA

Understanding of general regulatory and quality expectations.

Good scientific background communication skills including presentation and scientific / technical writing.

Languages :

Fluent English (Oral and written)

German as a plus

Accessibility and accommodation

Novartis is committed to working with and providing reasonable accommodation to all individuals. If because of a medical condition or disability you need a reasonable accommodation for any part of the recruitment process or in order to receive more detailed information about the essential functions of a position please send an e-mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Skills Desired

Key Skills

Healthcare Attorney,General Insurance,Attorney At Law,Core Banking,Import & Export,Airlines

Employment Type : Full-Time

Experience : years

Vacancy : 1

Créer une alerte emploi pour cette recherche

Science Technology • Basel, Basel-Stadt, Switzerland

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