Junior Process Expert

C046 (FCRS = CH046) Novartis Pharma Stein AG; Stein; Vor Ort; CHF 74.000 - 138.000; Teilzeit

Zusammenfassung

Novartis Pharma Stein AG is seeking a temporary 12-month role located in Stein to support deviations, complaints, CAPAs, and production issue decisions. You will assist in creating manufacturing instructions, maintain BOMs, and ensure GMP‑compliant documentation while contributing to SOP development and validation activities.

Fluency in English and German is required, and a degree in scientific disciplines is expected.

Qualifikationen

• Degree in scientific disciplines.
• Ability to work independently.
• Proficiency in Microsoft Office applications.
• Fluent in English and German.

Aufgaben

• Supports the handling of deviations, complaints, actions, and CAPAs.
• Provides support in decision‑making related to production issues.
• Assists in the creation and maintenance of manufacturing instructions, including bills of materials, process sub‑steps, and process steps.
• Supports the processing of quality notifications, including external and internal complaints.
• Assists in the development of specific SOPs.
• Ensures GMP‑compliant documentation.
• Adheres to GSU guidelines.
• Ensures cleanliness, hygiene, and order within the work environment.
• Assists in implementing corrective measures for deviations.
• Supports process and cleaning validations and assists with qualification activities (e.g., thermal requalification).

Kenntnisse

English language

German language

Independent working

Ausbildung

Degree in scientific disciplines

Master's degree (Desirable)

Tools

MS Office

Jobbeschreibung

Salary Range: CHF74,200.00 - CHF137,800.00

Job Description Summary

#LiOnSite Location: Stein

Major accountabilities

• Supports the handling of deviations, complaints, actions, and CAPAs.
• Provides support in decision‑making related to production issues.
• Assists in the creation and maintenance of manufacturing instructions, including bills of materials, process sub‑steps, and process steps.
• Supports the processing of quality notifications, including external and internal complaints.
• Assists in the development of specific SOPs.
• Ensures GMP‑compliant documentation.
• Consistently adheres to GSU guidelines.
• Ensures cleanliness, hygiene, and order within the work environment.
• Assists in implementing corrective measures for deviations.
• Supports process and cleaning validations and assists with qualification activities (e.g., thermal requalification).

Essential requirements

• Degree in Scientific disciplines.
• Ability to work independently.
• Proficiency in Microsoft Office applications.
• Fluent in English and German.

Desirable requirements

• Master's Degree.
• Initial experience in a GMP manufacturing environment.

Contract

We offer a temporary contract of 12 months.

Benefits

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. The rewards of being part of our team go far beyond base pay and incentives.We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave.

Salary

Expected Annual Base Salary Range for role: CHF 74.200 - 137.800

The salary offered is determined based on gender‑neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance‑based bonus depending on certain performance parameters. Further details will be provided during the application process. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read Our Brochure

Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

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 [e-mail] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Commitment to Diversity and Inclusion / EEO

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

Skills Desired Data Analytics

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.

China Cross‑Border Data Transfer (CBDT) Policy

In the context of China Cross‑Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov.