QC Analyst II (80-100%)*

Novartis Farmacéutica; Basel-Stadt; Vor Ort; CHF 80’000 - 100’000; Vollzeit

Zusammenfassung

A leading pharmaceutical company seeks a highly motivated QC Analyst II to manage laboratory tasks and ensure compliance with cGxP regulations. Candidates will execute bioanalytical testing and document processes while demonstrating attention to detail and collaboration.

Qualifikationen

• Experience in a bioanalytical laboratory in QC environment.
• Proficient in ELISA testing and data integrity standards.
• Strong administrative skills.

Aufgaben

• Manage sample storage and perform bioanalytical testing.
• Ensure compliance with cGxP regulations.
• Document stability samples to cGxP standards.

Kenntnisse

Attention to detail

Organizational skills

Collaboration

GMP compliance

Ausbildung

Completed apprenticeship as a laboratory assistant or equivalent training

Tools

Bioanalytical techniques

Jobbeschreibung

We are currently seeking a highly motivated individual to join our team as QC Analyst II. The successful candidate will be responsible for the execution of assigned tasks in our laboratory, ensuring compliance with cGxP regulations.

The ideal candidate will have a strong attention to detail, excellent organizational skills, and a passion for ensuring product quality.

About the Role

Key Responsibilities:

• Sample storage and management.
• Bioanalytical testing and documentation of API, drug substance, drug product, finished product, complaints, stability, packaging material samples.
• Ensure all activities are in compliance with cGxP, including data integrity.
• Stability: Testing storage and management and analytical documentation of stability samples to cGxP standards.
• Previous experience working in a bioanalytical laboratory in QC environment in the pharmaceutical industry. Excellent expertise in bioanalytical techniques (cell splitting, bioassay and ELISA testing, etc).
• Completed apprenticeship as a laboratory assistant or equivalent training.
• Collaborative and result-oriented mindset.
• Strong administrative skills and GMP compliance.
• Efficient production and documentation of tasks.
• Proficiency in breakthrough analysis and resilience.

This role is limited for 12 months.

Why Novartis

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other to achieve breakthroughs that change patients’ lives.

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.

Accessibility and Accommodation

Novartis is committed to working with and providing reasonable accommodation to all individuals. If you need a reasonable accommodation for any part of the recruitment process due to a medical condition or disability, please email [e-mail] with your request and contact information, including the job requisition number.

If this role is not suitable to your experience or career goals but you wish to stay connected about Novartis opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

*Disclaimer: Some restrictions on flexible working options may apply and will be discussed during the interview.

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right role for you? Sign up to our talent community to stay connected and learn about opportunities: https://talentnetwork.novartis.com/network