Principal Scientist limited until September 2027 (m/f/d)

Sandoz in Deutschland; Holzkirchen; Vor Ort; EUR 70.000 - 100.000; Vollzeit

Zusammenfassung

A leading global pharmaceutical company is seeking a Principal Scientist (m/f/d) in Holzkirchen. The role requires a PhD in Science or equivalent industry experience and involves designing and supervising research projects and maintaining laboratory standards. The ideal candidate has strong project management and leadership skills and is fluent in English. Benefits include 30 days of annual leave and personal growth opportunities.

Leistungen

30 days annual leave

Holiday allowance

Retirement schemes

Bike leasing

Qualifikationen

• PhD in Science with 2 years relevant experience, or Master's degree with 6 years relevant experience, or Bachelor's with 12 years industry experience.
• Strong scientific knowledge in manufacturing, analytical, and pharmaceutical areas.
• Knowledge of safety regulations and project management.

Aufgaben

• Design and monitor team activities and projects.
• Maintain tools and ensure compliance with standards.
• Write protocols and scientific documents for registration.

Kenntnisse

Project management

Scientific writing

Leadership skills

Laboratory tools proficiency

Fluent English

Ausbildung

PhD in Science

Master's degree

Bachelor's or equivalent

Tools

Laboratory equipment

Documentation software

Jobbeschreibung

Principal Scientist limited until September 2027 (m/f/d)

Join us to apply for the Principal Scientist limited until September 2027 (m/f/d) role at Sandoz in Deutschland.

Sandoz is undergoing an exciting transformation as a global leader in sustainable Biosimilar and Generic medicines. We offer unique professional and personal growth opportunities. Join us and help shape the future!

Your Key Responsibilities

Your responsibilities include, but are not limited to:

• Design, plan, perform, supervise, and monitor activities of teams and projects; handle multiple tasks; understand and meet customer needs.
• Own and maintain complex tools, equipment, or facilities; ensure infrastructure and equipment are properly maintained and investments are made as needed.
• Follow standards outlined in Quality Manual, SOPs, and HSE and ISEC guidelines; lead initiatives for compliance and continuous improvement; advise team members; align activities with clinical development processes.
• Interpret results, evaluate data, draw conclusions; supervise scientific and technical activities; review raw data; perform complex tasks without established procedures.
• Write protocols, scientific reports, SOPs, and documents for external partners and registration purposes; interact with authorities as needed.
• Communicate and resolve problems, lead transfer of know-how, and train external or internal teams; travel up to 5% may be required.
• Contribute to budget and resource planning.
• Develop and optimize scientific methods and processes; lead technology development and implementation.
• Provide scientific guidance, conduct literature searches, foster knowledge exchange, mentor colleagues, and contribute to publications and presentations.
• Lead sub-teams, represent the function in technical teams, and ensure project responsibilities are met.
• Collaborate across groups, resolve conflicts with empathy.

Essential Requirements

What you’ll bring to the role:

• PhD in Science with 2 years relevant experience, or
• Master's degree with 6 years relevant experience, or
• Bachelor's or equivalent with 12 years industry experience.
• Knowledge of safety regulations and safe handling of chemicals and equipment.
• Understanding of development activities within own function and related functions.
• Strong scientific knowledge in relevant areas (manufacturing, analytical, pharmaceutical).
• Project management and leadership skills.
• Knowledge of regulatory guidelines and expectations.
• Proficiency with laboratory/technical tools, software, and documentation.
• Excellent presentation and scientific writing skills.
• Fluent in English; basic skills in local language as required.

What You’ll Receive

Sandoz offers personal growth opportunities through platforms like Coursera, along with benefits such as:

• 30 days annual leave
• Holiday allowance
• Special occasion rewards
• Retirement schemes and capital formation benefits
• Parental leave
• Additional benefits like bike leasing

Why Sandoz?

As a leader in generic and biosimilar medicines, Sandoz has provided treatments to over 900 million patients in 100+ countries in 2024. We aim to do more by investing in development, production, and partnerships to make medicines accessible and affordable worldwide.

Our culture is collaborative, inclusive, and driven by talented colleagues. We support diverse, flexible careers and personal development.

Commitment to Diversity & Inclusion

We strive to build an inclusive environment and diverse teams that reflect the communities we serve. Hiring decisions are based solely on qualifications. We accommodate applicants with disabilities and encourage them to inform us in advance if needed.