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Novartis

Quality Control Specialist

Novartis is hiring a Quality Control Specialist in Hyderabad, India. Level rates it ; you can apply on Novartis.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • The posting mentions SAP S 4hana, quality control and gmp among its tools and skills.
  • Level classes it as a mid-level role.
  • Novartis has 864 other open roles on Level.
  • Posted within the past week.

AI in this role

A quality control specialist role supporting laboratory processes, compliance, and digital systems in a regulated environment.

SAP S 4hana
quality-controlgmplaboratory-operationsroot-cause-analysis

Job Description Summary

#LI-Hybrid

Location: Hyderabad, India

Relocation Support: This role is based in Hyderabad, India. Novartis is unable to offer relocation support: please only apply if accessible.

Great laboratories rely on more than advanced equipment. They rely on people who make quality, compliance, and continuous improvement part of every process. As a Quality Control Specialist, you’ll help strengthen laboratory operations by supporting equipment, documentation, analytical processes, and digital systems within a regulated environment. You’ll collaborate across functions, use tools such as SAP S/4HANA, and identify opportunities to make laboratory processes more efficient and reliable, helping ensure quality is built into the way we work every day.


Job Description

Obligatory Requirements:


  • Support the introduction and continuous improvement of laboratory processes, analytical techniques, and equipment.
  • Prepare, review, and maintain laboratory procedures and equipment-related documentation.
  • Ensure laboratory activities comply with Good Manufacturing Practice requirements and internal quality standards.
  • Use digital systems to strengthen documentation, reporting, tracking, and process efficiency.
  • Support equipment and asset management activities using SAP S/4HANA and other relevant systems.
  • Identify deviations and contribute to investigations, root-cause analysis, and effective corrective actions.
  • Collaborate with cross-functional teams to ensure reliable, compliant, and efficient laboratory operations.
  • Identify improvement opportunities that strengthen equipment performance, quality compliance, and operational effectiveness.

Essential Requirements:


  • University degree in Pharmacy, Chemistry, Engineering, Mechatronics, Natural Sciences, or another relevant discipline.
  • At least two years of relevant experience in a regulated laboratory, quality, production, or development environment.
  • Strong understanding of Good Manufacturing Practice requirements and quality standards.
  • Strong digital literacy with confidence using information technology systems, databases, and business applications.
  • Ability to work independently while collaborating effectively across cross-functional teams.
  • Proficiency in English, with strong communication, organizational, and coordination skills.

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards

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.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network.


Skills Desired

How we rate this

Quality Control Specialist 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.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

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

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Quality ControlGmpLaboratory OperationsRoot Cause AnalysisSAP S 4hana

Questions you could be asked

  1. Tell me about a project where quality control was part of your work. What did you do?
  2. Tell me about a project where gmp was part of your work. What did you do?
  3. Tell me about a project where laboratory operations was part of your work. What did you do?
  4. Tell me about a project where root cause analysis was part of your work. What did you do?
  5. Walk me through how you've used SAP S 4hana in your day-to-day work.

Adapt your resume

  • List these exact terms on your resume: Quality Control, Gmp, Laboratory Operations, Root Cause Analysis, and SAP S 4hana. 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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