Quality Control Analyst (Temporary )

BandLevel 2

Job Description Summary#LI-Onsite

Location: Zaragoza – La Almunia, Spain

Relocation Support: This role is based in Zaragoza – La Almunia, Spain. Novartis is unable to offer relocation support: please only apply if accessible.

Bring quality to life in a role where your expertise safeguards patient health. As a Quality Control Analyst, you will ensure products meet the highest standards of safety and compliance while working in a dynamic laboratory environment.

This is a temporary opportunity where your analytical skills will directly support the release and stability of pharmaceutical products, contributing to Novartis’ mission to reimagine medicine, with availability required to support a 24/7 operation.

Job Description

Key Responsibilities

Perform analytical testing of drug products, finished goods, and materials following approved procedures and standards

Document laboratory activities and results accurately in line with Good Manufacturing Practice requirements

Manage sample storage, tracking, and handling to ensure integrity and compliance

Conduct stability testing and maintain proper documentation of stability studies

Investigate and report technical complaints, adverse events, and quality issues within 24 hours

Ensure full adherence to Standard Operating Procedures and regulatory guidelines at all times

Support audit and inspection readiness through consistent compliance and documentation practices

Monitor deadlines and ensure timely completion of all testing and reporting activities

Identify and implement process improvements to enhance efficiency and reduce operational costs

Collaborate with cross-functional teams to maintain quality standards and resolve issues effectively

Essential Requirements

Degree in Chemistry, Pharmacy, or a related scientific field

Experience in quality control within a pharmaceutical or regulated manufacturing environment

Knowledge of Good Manufacturing Practice and quality standards

Hands-on experience with analytical laboratory techniques and equipment

Ability to follow Standard Operating Procedures with high attention to detail

Strong problem-solving skills and ability to manage competing priorities

Intermediate level of English, with good reading and writing skills

Desirable Requirements

Experience with stability testing and lifecycle management of pharmaceutical products

Familiarity with audit and inspection processes within regulated environments

Commitment to Diversity and Inclusion:

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

Skills DesiredCollaboration, Communication Skills, Data Integrity, Deadline Adherence, Dealing With Ambiguity, Decision Making, Digital saviness, Leadership, Problem Solving Skills, Regulatory Requirements knowledge

REQ-10078372