Job Description

Band

Level 1This temporary role involves utilizing chemistry laboratory skills to sampling incoming (Excipients, APIs and Packaging materials) materials. The Quality Control Analyst ensures all sampling of incoming materials are conducted in compliance with established Standard Operating Procedures (SOPs) and validated analytical methods.

Major Accountabilities:

• Manage sampling process of incoming materials (Excipients, APIs, microbiology and Packaging materials) in compliance with GxP standards.
• Perform sampling process and documentation of incoming materials according to GxP requirements.
• Report technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt.
• Ensure continuous inspection readiness and adherence to GMP, GSU guidelines, and SOPs.
• Identify and implement cost-saving opportunities and process optimizations.
• Complete all required training activities.

Essential Requirements:

• Strong technical and scientific background in pharmaceutical or chemical fields.
• Hands-on experience in a laboratory setting within the pharmaceutical, analytics, or quality control environment.
• Associate Degree or High school graduate in Chemistry or related field

Benefits and Rewards:

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: Novartis Life Handbook

Commitment to Diversity & Inclusion:

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

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

Skills Desired

Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Health & Safety Regulations Knowledge, Leadership, Problem Solving Skills, Punctuality, Regulatory Requirements knowledge