Novartis
pharmaceutical
QualityControlAnalyst(TemporaryPosition)
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Control Analyst (Temporary Position) at Novartis. Skills: Quality Control, Analytical Testing, Good Manufacturing Practice, Pharmaceutical Manufacturing. 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”
Industry & Context.
problem-solving skills; Problem Solving Skills; resolve issues effectively
availability required to support a 24/7 operation, availability to work rotating shifts, including mornings, afternoons, and nights
What They're Looking For.
Must Have
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, problem-solving skills, Intermediate level of English, with good reading and writing skills
Nice to Have
Experience with stability testing and lifecycle management of pharmaceutical products, Familiarity with audit and inspection processes within regulated environments
What You'll Do.
Perform analytical testing of drug products
and materials following approved procedures and standards
Document laboratory activities and results accurately in line with Good Manufacturing Practice requirements
Manage sample storage
and handling to ensure integrity and compliance
Conduct stability testing and maintain proper documentation of stability studies
Investigate and report technical complaints
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
How You'll Work.
Team & Collaboration
Collaborate with cross-functional teams to maintain quality standards and resolve issues effectively
Communication Scope
Communication Skills; Intermediate level of English, with good reading and writing skills
Process & Methodology
Monitor deadlines, ensure timely completion of all testing and reporting activities
Full Job Description
**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. This role requires availability to work rotating shifts, including mornings, afternoons, and nights. **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 regulat
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