QC Supervisor

QC Supervisor

REQ-10031253
Nov 25, 2024
Italy

About the Role

Major accountabilities:

  • OOx/Deviation handling .
  • CAPA definition -KPI trending -Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) Stability -Stability testing (Projects) – protocol preparation, evaluation, report preparation .
  • Reporting (Stability plan preparation, trend analysis, evaluation) -Performance of Stability studies, protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release) -Microbiological QC -Perform Microbiological testing of materials and utilities, environmental and personnel monitoring -Provide expert Support for site qualification and validation activities -Maintain and calibrate equipment incl. plan preparation -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

  • The relevant KPIs that are defined in the Quality Control areas apply: e.g. analytical lead times -Timely and GMP-compliant analysis & documentation of the results.
  • Error rate: Number of OOS (analysis errors) related to the number of analyzes -No complaints about official inspections.
  • Individual performance is assessed using the PMP performance dialog together with the manager   

Minimum Requirements:
Work Experience:

  • Functional Breadth.
  • 3-5years experience in Pharma/Manufacturing sector in analytical lab in.
  • Collaborating across boundaries.
  • a GMP environment/equivalent.

Skills:

  • Continuous Learning.
  • Dealing With Ambiguity.
  • Decision Making Skills.
  • Gxp.
  • Industry Standards.
  • Laboratory Equipment.
  • Laboratory Excellence.
  • Quality Control (Qc) Testing.
  • Quality Control Sampling.
  • Self Awareness.
  • Technological Expertise.
  • Total Quality Management.

Languages :

  • English.

Role Requirements

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

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

Operations
Innovative Medicines
Italy
Ivrea
Quality
Full time
Regular
No
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REQ-10031253

QC Supervisor

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  2. https://www.novartis.com/about/strategy/people-and-culture
  3. https://talentnetwork.novartis.com/network
  4. https://www.novartis.com/careers/benefits-rewards
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