367215BR
Mar 17, 2023
Slovenia
Job Description
175,000,000+ pieces are packed annually for our patients! Join us in the Production Support Department as a Process expert responsible for packaging sterile products. If you want dynamic work in a young, energetic team, we invite you to join us!
Your key responsibilities:
• Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements.
• Responsible for maintaining the master manufacturing documents of assigned products (e.g. Master Batchb Record, Bill of Material (BOM) & Recipe, Quality Risk Assessment, Zurich Hazard Analysis)
• Support steward for assessment of technical changes, establishment of root-cause analysis, Quality Risk Assessment, process control strategy.
• Ensure that all process changes in assigned products are managed through appropriate change control procedure.
• Perform first line evaluation of product and process related issues (deviations, complaints, OOS, OOE).
• Maintain processes at inspection readiness level.
• Review validation protocols and reports for technical correctness.
• Support the execution of process validations, and short-term improvement projects, liaising with all the relevant parties at shop floor to ensure accurate execution.
• Execute process improvements and scale-up.
Your key responsibilities:
• Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements.
• Responsible for maintaining the master manufacturing documents of assigned products (e.g. Master Batchb Record, Bill of Material (BOM) & Recipe, Quality Risk Assessment, Zurich Hazard Analysis)
• Support steward for assessment of technical changes, establishment of root-cause analysis, Quality Risk Assessment, process control strategy.
• Ensure that all process changes in assigned products are managed through appropriate change control procedure.
• Perform first line evaluation of product and process related issues (deviations, complaints, OOS, OOE).
• Maintain processes at inspection readiness level.
• Review validation protocols and reports for technical correctness.
• Support the execution of process validations, and short-term improvement projects, liaising with all the relevant parties at shop floor to ensure accurate execution.
• Execute process improvements and scale-up.
Diversity & Inclusion / EEO
Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Minimum Requirements
What you will bring to the role:
• BSc. in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree.
• Minimum 2 year experience in process support role on the shop floor of GMP manufacturing or QA/QC.
• Fluent in local and English language.
• Knowledge of Microsoft Office.
Desirable Requirements:
• Knowledge of SAP, Trackwise, Verum.
You’ll receive:
Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), employment at Top SI Employer, Unlimited learning and development opportunities.
We offer permanent employment, with 6 months of probation period and possibility of extension.
You are kindly invited to submit your application in English language, including CV by 10th of April 2023.
Why Novartis?
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Novartis!
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve.
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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
• BSc. in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree.
• Minimum 2 year experience in process support role on the shop floor of GMP manufacturing or QA/QC.
• Fluent in local and English language.
• Knowledge of Microsoft Office.
Desirable Requirements:
• Knowledge of SAP, Trackwise, Verum.
You’ll receive:
Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Energized for Life), employment at Top SI Employer, Unlimited learning and development opportunities.
We offer permanent employment, with 6 months of probation period and possibility of extension.
You are kindly invited to submit your application in English language, including CV by 10th of April 2023.
Why Novartis?
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Novartis!
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve.
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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
Novartis Technical Operations
NTO SANDOZ TECHOPS
Slovenia
Ljubljana
LEK SVN
Technical Operations
Full Time
Regular
No
