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Senior Scientist AD - IVIVC & Bioassays (d/f/m)

Remote:

Full Remote

Contract:

Full time

Experience:

Senior (5-10 years)

Work from:

Slovenia

Offer summary

Qualifications:

Advanced degree in molecular biology, biochemistry, pharmacy, Practical knowledge of cell-based assays, Knowledge in surface plasmon resonance is desirable, Active English language skills required.

Key responsabilities:

Develop and manage various in-vitro methods for characterization and specification of products
Interpret experimental results and prepare scientific reports
Qualify established and develop novel in-vitro assays
Interact with external laboratories and project teams
Ensure adherence to regulatory and quality standards

Novartis Healthtech: Health + Technology XLarge https://www.novartis.com/

10001 Employees

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Job description

Job Description Summary

The future is ours to shape.

Job Description

Sandoz, of which Lek is also a part, is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Generic and Biosimilar medicines.

Now as an independently listed company, Sandoz aims to increase its strategic focus, operate with greater agility, set clearer business objectives, enhance shareholder returns, and strengthen its culture for us, the Sandoz and Lek associates. This is an exciting time in our history, and by creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally.

We are looking for a Senior Scientist AD who will join our In-vitro & in-vivo (IVIVC) correlation group in Pharmaceutical Development of the Sandoz Development Center Slovenia! In this role, you will support development and management of various in-vitro methods (potency assays and other relevant bioassays) to both characterization and specification purposes of generic complex products. Join us as a Founder of our ‘new’ Sandoz and Lek! 

Your key responsibilities:

Your responsibilities include, but not limited to:

Provision of expert knowledge for bioassays and evaluation of literature data on biological activity testing of peptides, aptamers & oligonucleotides as well as complex drug formulations (e.g. nanoparticles, liposomes, microspheres).
Development and qualification of cell - based biological assays using immortal and primary cell lines or ready to use bioassay kits in relation with different analytical techniques (e.g., ELISA, fluorescence/luminescence spectrophotometry etc.).
Independent interpretation of experimental results of in-vitro biological responses (ligand binding assays, antigen binding assays etc.).
Qualification of established in vitro assays (e.g. permeability) and development and qualification of novel in-vitro assays (e.g., gut on a chip models, organoids). supporting in-vivo predictions
Preparation of scientific reports and documents, coordinating and delivering high-quality source documents for submission and review of regulatory documents.
Generate or revise protocols and reports, SOPs, forms, laboratory data sheets, as well as provide mentoring and support to laboratory associates.
Interact effectively with external partner laboratories and foster strong collaboration within project teams.
Ensure adherence to regulatory requirements, quality standards, and health, safety, and environmental (HSE) standards in work practices.

What you will bring to the role:

Advanced degree (desirable PhD) in molecular biology, biochemistry, pharmacy or other relevant discipline.
Scientific and practical knowledge with cell-based assays (e.g., flow cytometry, ELISA, LC-MS, fluorescence/luminescence etc.). Knowledge in the field of surface plasmon resonance is desirable.
Ability to communicate in an open, clear, assertive, organized, and concise manner to be influential in scientific meetings and ability to work together as one team in a global environment.
Active knowledge of English language required (oral & written).

You’ll receive:

Employment at the most reputable employer in Slovenia offers Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), Unlimited learning and development opportunities. 

Possible job locations: Slovenia (Ljubljana) 

We offer permanent contract with 6-month of probation period. You are kindly invited to submit your application in English language, including CV, by 8 November 2024.

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!

The future is ours to shape!

Commitment to Diversity & Inclusion:

Sandoz is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. 

Join our Sandoz Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: https://talentnetwork.novartis.com/sandoztalentpool

#Sandoz

Skills Desired