OT Quality Associate
Novartis is hiring an OT Quality Associate. It pays €61k-€114k a year and Level rates it ; you can apply on Novartis.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- Tools and skills the posting cites include PLC, SCADA and quality assurance.
- Level classifies it as a senior role.
- Level lists 864 other open roles at Novartis.
AI in this role
Ensure an audit-ready operational technology environment and manage OT quality processes at a pharmaceutical site in Belgium.
Salary Range:
€61,300.00 - €113,900.00
Job Description Summary
Location: Puurs, Belgium #LI-Hybrid 3 days/week in officeInternal job title: OT Quality Associate
This role is based in Belgium. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
About the Role:
The OT Quality Associate will join our site in Puurs and will be responsible for ensuring an audit-ready OT environment through the development, maintenance, and continuous improvement of procedures, work instructions, and operational handbooks, as well as conducting quality reviews and supporting internal and external audits.
Job Description
Key Responsibilities:
Responsible for User Access reviews and management of user groups; Technical audit trail reviews (TATR); Incident reviews.
Support and follow-up of CAPAs and deviations, verify and update OT procedures, restructure these SOPs, including creation of a clear graphical overview and interlinking; manage Automation Operational Handbooks, Create AOHs for our most important OT systems.
Manage exceptions, including patching and shared privileged accounts.
Manage server licenses and certificates.
Manage Vendor onboarding (VSQAPS) and vendor support.
Support internal and external audits.
Strategy & Organizational development: Support internal and external audits, and lead or contribute to improvement projects for equipment, utilities and facilities
Supplier & Contract Management: Select suppliers and contractors while taking the appropriate strategy into account; establish supplier contracts, SLAs and MSCs; manage project suppliers, contractors and third parties.
Essential Requirements:
Degree in engineering (Dipl. Ing. / M.Sc. / B.Sc.) or equivalent.
5+ years experience in OT Quality / CSV essential, including 3+ years of experience in pharma.
Good experience and understanding in PLC, SCADA, automation, CSV, OT CSV
Experience in User Access reviews and management of user groups; Technical audit trail reviews (TATR); Incident reviews.
Project management and technical knowledge, including automation, with proven ability to deliver safe, effective and fully compliant projects.
Advanced HSE and GxP / QA knowledge.
Fluent in English and Dutch.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network
Accessibility and accommodation:
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because 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 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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: 61,300.00 EUR to 113,900.00 EUR
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.
Skills Desired
Business Continuity, Cost Management, Decision Making, Operational Excellence, Problem Solving, Project Management, Quality Compliance, Risk Management, Stakeholder Management, Vendor ManagementHow we rate this
OT Quality Associate 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.
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. 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
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 csv was part of your work. What did you do?
- Tell me about a project where ot was part of your work. What did you do?
- Tell me about a project where gxp was part of your work. What did you do?
- Tell me about a project where compliance was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Quality Assurance, Csv, Ot, Gxp, and Compliance. 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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