Level

Novartis

Quality Assurance Operations Specialist

Novartis is hiring a Quality Assurance Operations Specialist. It pays €44k-€82k a year and 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, gmp and quality assurance among its tools and skills.
  • Level classes it as a mid-level role.
  • Novartis has 835 other open roles on Level.

AI in this role

Provide quality assurance support for 24/7 shopfloor GMP activities and batch release processes in a manufacturing environment.

sap
gmpquality-assurancebatch-releasedeviation-investigation

Salary Range:

€44,100.00 - €81,900.00


 

Job Description Summary

#LI-Onsite

Location: Baarle Nassau, Netherlands

We are seeking a detail-oriented Quality Assurance Operations Specialist to join our team in Baarle-Nassau, Netherlands. This role supports a 24/7 shift-based operation, so candidates must be comfortable working assigned shifts, including days, evenings, nights, weekends, and bank holidays as required.

The Quality Assurance Operations Specialist provides QA support for all shopfloor GMP-related activities. The primary focus of the role is to support the timely batch release process and related operational activities, ensuring that batches are released in accordance with regulatory requirements and the local quality system. Responsibilities range from material release and batch record review to deviation support and technical QA support, including activities such as calibrations and interventions


 

Job Description

Willingness and availability to work on shifts, including days, evenings, nights, weekends, and bank holidays, is required.


Major Accountabilities:

  • Prepare and perform QA review of batch release documentation and support the Quality Responsible in the batch release process.
  • Provide on-site QA support for shopfloor GMP activities, including interventions, calibrations, and other operational activities.
  • Ensure compliant documentation lifecycle management, including review, approval, archiving, and control of paper-based and electronic records.
  • Review and release starting materials and incoming goods in accordance with applicable procedures and GMP requirements.
  • Review and approve quality-related documentation, including operational procedures, protocols, work instructions, and controlled documents.
  • Support deviation, OOS, OOT, OOE, and System Suitability Test failure investigations, including impact assessments, follow-up, and timely closure.
  • Support CAPA, action, change control, internal audit, and Health Authority inspection readiness activities, ensuring timely execution of defined actions.

​

Obligatory requirements: ​

  • Education: MBO or HBO level, preferably in a scientific, pharmaceutical, life sciences, or related field.
  • Solid knowledge of GMP quality systems.
  • Basic knowledge of applicable regulatory requirements.
  • Strong affinity with and awareness of quality topics.
  • Excellent organizational skills with strong attention to detail.
  • Ability to work effectively in a team and communicate clearly with cross-functional stakeholders.
  • Demonstrates an appropriate sense of urgency and the ability to prioritize tasks in a dynamic operational environment.
  • Fluent in English, both written and spoken.

Desirable requirements:

  • Experience with radiation, PET or radiopharmaceuticals is highly valued.

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.


Expected Annual Base Salary Range for role: €44,100 to €81,900.

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.


In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.


The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.


Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.


Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.


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 Desired

How we rate this

Quality Assurance Operations 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

GmpQuality AssuranceBatch ReleaseDeviation InvestigationSAP

Questions you could be asked

  1. Tell me about a project where gmp was part of your work. What did you do?
  2. Tell me about a project where quality assurance was part of your work. What did you do?
  3. Tell me about a project where batch release was part of your work. What did you do?
  4. Tell me about a project where deviation investigation was part of your work. What did you do?
  5. Walk me through how you've used SAP in your day-to-day work.

Adapt your resume

  • List these exact terms on your resume: Gmp, Quality Assurance, Batch Release, Deviation Investigation, and SAP. 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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