Position: Associate

Job type: Full-time

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Job content

About The Role

31! Million Tablets and Capsules every year to supply clinical studies and support technical development of innovative oral products. Join our team to guarantee the best quality and highest reliable delivery of our products for the patients in the clinics. There you make a difference.

You will be responsible for engineering activities including planning and coordination of maintenance & calibration activities, project execution and continuous improvement at site level (e.g. buildings, process equipment, utilities, automation).

Your responsibilities:
  • Ensure equipment operates to required HSE, Quality, Environmental and Reliability standards
  • Act as key engineer for the equipment at area of responsibility
  • Establish cost efficient repair and maintenance processes. Implement FMECA and optimize maintenance for the asset depending on equipment criticality
  • Plan resources and coordinate preventive & corrective maintenance / calibration activities. Plan spare parts and lead stores
  • Lead / execute continuous improvement and investment projects in alignment with local and global stakeholders.
  • Ensure sharing and leverage of best practices and expertise within the Novartis engineering community. Provide technical trouble shooting
  • Develop and implement periodic requalification plan. Build site SOPs & templates. Support internal and external audits
  • Deviation Investigator (Root Cause Analysis, define and complete CAPA Plan)
Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Role Requirements

What you bring to the role:
  • Degree in engineering (Dipl. Ing. / M. Sc. / B. Sc.) or equivalent (e.g. mechanical, automation)
  • 3 years proven track record as an engineer in a GMP environment Experience in Pharma/Manufacturing plant environment. Knowledge in small molecule drug product (DP) technologies (e.g. encapsulation, precise drug product filling encapsulation) are an advantage
  • Strong communication and problem-solving skills, flexibility as well as the ability to work independently
  • Proficient in both, English and German (written and spoken)
Division

Global Drug Development

Business Unit

TECHNICAL R & D GDD

Work Location

Basel

Company/Legal Entity

Novartis Pharma AG

Functional Area

Technical Operations

Job Type

Full Time

Employment Type

Regular

Shift Work

No

Early Talent

No
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Deadline: 01-06-2024

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