QC Analyst I

Perform analytical testing of API, drug substance, drug product, finished product, packaging material, complaint, and stability samples. Manage sample receipt, storage, tracking, and documentation. Ensure all laboratory activities are conducted in compliance with cGxP/GMP requirements and data integrity standards. Execute laboratory activities including analysis, equipment maintenance, calibration, and qualification. Support stability testing and stability sample management. Maintain accurate analytical documentation and records. Participate in inspections and maintain audit readiness. Identify and report HSE risks, incidents, and improvement opportunities. Complete required training and adhere to all HSE and GMP procedures. Contribute to continuous improvement and laboratory process optimization.

Welcome to where we thrive together! Are you ready to join a community where you can make a real impact on the world through your exceptional communication skills? At Novartis, we believe in creating a positive and inclusive work environment where we can solve the toughest healthcare challenges together.

• Degree, apprenticeship, or equivalent qualification in Chemistry, Biochemistry, Pharmacy, Life Sciences, or a related scientific field.

• Initial experience working in a laboratory environment, preferably within a GMP-regulated industry.

• Basic understanding of cGxP/GMP requirements and data integrity principles.

• Experience with analytical testing and accurate documentation of laboratory activities.

• Strong attention to detail and commitment to quality and compliance standards.

• Ability to follow SOPs and work effectively in a regulated environment.

• Good communication skills and ability to collaborate within cross-functional teams.