You manage and test samples, ensuring compliance with regulatory standards while documenting essential data for various products.
Anforderungen
- •Previous experience in bioanalytical laboratory
- •Completed apprenticeship as laboratory assistant
- •Collaborative and result-oriented mindset
- •Strong administrative skills and GMP compliance
- •Efficient production and documentation of tasks
- •Proficiency in breakthrough analysis and resilience
Deine Aufgaben
- •Manage sample storage and documentation.
- •Conduct bioanalytical testing of various samples.
- •Document API, drug substance, and product details.
- •Ensure compliance with cGxP and data integrity.
- •Perform stability testing and documentation.
Deine Vorteile
Handbook for personal and professional growth
Original Beschreibung
# QC Analyst II (80-100%)*
**Basel (City)** | **Full time**
**Job Description Summary**
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.
**Job Description**
**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.
**Essential Requirements:**
* 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.
**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, 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 diversity.inclusion\_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
**\*Disclaimer:** Some restrictions on flexible working options may apply and will be discussed during interview if applicable.
**Skills Desired**
Continued Learning, Dealing With Ambiguity, Decision Making Skills, Gxp, Industry Standards, Laboratory Equipment, Laboratory Excellence, Quality Control (Qc) Testing, Quality Control Sampling, Self-Awareness, Technological Expertise, Total Quality Management