Scientist - Technical Development

Healthcare Businesswomen’s Association; Rudolstadt; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

Join a leading global provider of sustainable Generic and Biosimilar medicines as a key contributor in developing robust dosage forms. This role involves leading projects, managing experiments, and collaborating across departments to ensure high-quality outcomes. With a commitment to personal growth and a diverse work environment, you will have access to extensive learning resources and company benefits. Shape the future of Sandoz and help improve patient access to medicines.

Leistungen

30 days of annual leave

Holiday allowance

Additional rewards for special occasions

Company pension schemes

Parental leave

Bike leasing

Qualifikationen

• Minimum of 6 years relevant experience in industry.
• Understanding of experiment and validation design.

Aufgaben

• Lead and execute defined work packages for dosage form development.
• Design and manage experiments, ensuring compliance with GMP.
• Communicate and solve problems within own and broader areas.

Kenntnisse

Fluency in English

Strong scientific skills

Strong communication and presentation skills

Proven ability to manage and prioritize multiple projects

Ausbildung

BSc., MSc, or higher scientific degree

Tools

MS Office

statistical programs

Jobbeschreibung

Job Description Summary

Sandoz 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 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.

Join us as a Founder of our ‘new’ Sandoz!

Job Description

Major accountabilities:

1. Lead and execute defined work packages of medium/low complexity, or high complexity work packages with supervision, aiming at the development of stable, bioequivalent, robust, and cost-competitive dosage forms.
2. Design and manage experiments/batches, provide related scientific documentation.
3. Plan and execute experiments in accordance with quality risk management and Good Development Practice / GMP.
4. Assist in the preparation of and review the technological parts of dossiers.
5. Connect development data of different analytical origins of low/medium complexity, or high complexity with supervision, into meaningful conclusions.
6. Actively support the development of hard-to-make pharmaceutical products.
7. Communicate, address, and solve problems (e.g., deviations and unexpected results from experiments) within own and broader areas of responsibility, communicate effectively across organizational interfaces, lead the transfer of know-how or procedures to other departments or external contractors, including troubleshooting and on-site training, which may require travel.
8. Report and present scientific/technical results internally and contribute to publications, presentations, and patents.

What you’ll bring to the role:

1. BSc., MSc, or higher scientific degree with relevant professional experience or Apprenticeship in industry (or equivalent technical education) with a minimum of 6 years relevant experience in industry.
2. Fluency in English, German is a plus.
3. Relevant experience from development of final dosage forms.
4. Strong scientific skills allowing the drawing of accurate assumptions from limited data to assess the next step in a development program.
5. An understanding of experiment and validation design and the requirements when documenting protocols for these exercises.
6. An understanding of the parameters involved in scaling up formulation processes.
7. Technical/scientific protocol and report writing skills.
8. Knowledge of DoE (Design of Experiments), QbD (Quality by Design), and quality risk management.
9. Strong communication and presentation skills.
10. Proven ability to manage and prioritize multiple projects.
11. Good knowledge of relevant software tools (e.g., MS Office, statistical programs).

You’ll receive:

Sandoz has an employee-first approach, and that’s why your personal growth is so important to us. You will have access to Coursera and other learning platforms with more than 200,000 learning videos and 5,000+ courses.

In addition to the various learning opportunities, we offer company benefits, such as:

• 30 days of annual leave
• Holiday allowance
• Additional rewards for special occasions (e.g., service length awards, marriage celebration, etc.)
• Company pension schemes and capital formation benefits
• Parental leave
• Other offerings, such as bike leasing

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

The future is ours to shape!

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Hiring decisions are only based on the qualification for the position, regardless of gender, ethnicity, religion, sexual orientation, age, and disability.

The law provides for severely disabled/equal applicants the opportunity to involve the local representative body for disabled employees (SBV) in the application process. If you would like to request this, please let us know in advance as a note on your CV.

Join our Sandoz Network:

If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Sandoz and our career opportunities, join the Sandoz Network here:

https://talentnetwork.novartis.com/hiringgermany

#Sandoz

Skills Desired

Environment, Experiments Design, Health And Safety (EHS), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, SOP (Standard Operating Procedure), Technical Writing, Waterfall Model