QC Analyst II

AI in this role

Perform pharmaceutical laboratory testing and manage quality compliance systems.

hplcgctitrationempowerchromeleontiamo

quality-assurancegmpanalytical-testingdata-integrity

Salary Range:

63 980,00 CHF - 118 820,00 CHF

Job Description Summary

We are looking for a dedicated QC Analyst to support Good 'x' Practice (GxP) activities in our quality department. This role involves managing quality systems, implementing operational processes and ensuring compliance with Novartis quality standards.

This role is limited to 24 months.

Job Description

Key Responsibilities:

Maintain compliance with current Standard Operating Procedures (SOPs), GxP-compliant documentation, and records within the Novartis quality management system.
Perform and evaluate analytical tasks in a pharmaceutical laboratory, including working in shifts where necessary.
Ensure the integrity of all quality assurance records and data, as applicable, and foster collaboration between your team and other functions and departments.
Ensure an appropriate level of education and GxP knowledge.
Support quality audits and health authority inspections.

Essential Requirements:

Experience in quality assurance and analytical skills.
Proficiency in analytical technologies (e.g., HPLC, GC, titration).
Knowledge in the use of lab-specific software (e.g., Empower, Chromeleon, TiAmo).
GMP experience and technological expertise.
Willingness to work in shifts.
Fluency in German and good English.

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

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, be-cause 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.

Skills Desired

Collaboration, Communication Skills (Inactive), Data Integrity, Deadline Adherence, Digital saviness (Inactive), Health & Safety Regulations Knowledge (Inactive), Leadership, Managing Ambiguity, monitoring (Inactive), Problem Solving Skills (Inactive), Punctuality, Regulatory Requirements knowledge (Inactive)

How we rate this

QC Analyst II at Novartis rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

●●●● Builds AI80 to 100
●●●○ Works on AI60 to 79
●●○○ Uses AI40 to 59
●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

A free preview built only from this posting: what it asks for, what you could be asked in an interview, and how to adjust your resume.

Skills and AI tools this role asks for

Quality AssuranceGmpAnalytical TestingData IntegrityHplcGcTitrationEmpower

Questions you could be asked

Tell me about a project where quality assurance was part of your work. What did you do?
Tell me about a project where gmp was part of your work. What did you do?
Tell me about a project where analytical testing was part of your work. What did you do?
Tell me about a project where data integrity was part of your work. What did you do?
Walk me through how you've used Hplc in your day-to-day work.

Adapt your resume

List these exact terms on your resume: Quality Assurance, Gmp, Analytical Testing, Data Integrity, and Hplc. An applicant tracking system matches the wording, not the idea.
Attach one line of real, concrete experience to at least one of them — a tool named with nothing behind it rarely survives a human read.

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