385760BR
dub 10, 2024
Slovenia
About the Role
Location: Mengeš #LI-Onsite
We bring life-saving medicines to millions of people. We are at the crossroads of the latest advances in medical science and innovative digital technology. Everything we do is in line with our commitment to quality and to providing safe active substances for patients. Our commitment to quality is based on science, we innovate and our work is patient-centred. Whether you are involved in development, production, maintenance, compliance or analysis, your contribution will have a direct impact on patients. Without quality checks and quality assurance at all points in the process, we cannot reliably build patient trust. Do you value this mission?
As a QC Specialist III you will be responsible for planning, preparation, implementation and appropriate documentation of demanding physicochemical and biochemical analysis and preparation of analytical documentation in order to provide timely and quality analytical support for the smooth running of production processes. Acting in accordance with the law, internal regulations, Good Practices, and business objectives.
Key Responsibilities:
• Review, verification and approval of laboratory records and results.
• Ensure all activities in compliance with cGxP, and with data integrity. Perform Quality Control (QC) oversight activities.
• Manage OOx / analytical deviations and complaints and defining Corrective and Preventive Actions (CAPA).
• Participation in all training relevant to the position, maintenance of the relevant training evidence.
• Participation in inspections (interpretation of primary data and working method).
• Other tasks as assigned by the supervisor, and tasks based on a specific appointment.
We bring life-saving medicines to millions of people. We are at the crossroads of the latest advances in medical science and innovative digital technology. Everything we do is in line with our commitment to quality and to providing safe active substances for patients. Our commitment to quality is based on science, we innovate and our work is patient-centred. Whether you are involved in development, production, maintenance, compliance or analysis, your contribution will have a direct impact on patients. Without quality checks and quality assurance at all points in the process, we cannot reliably build patient trust. Do you value this mission?
As a QC Specialist III you will be responsible for planning, preparation, implementation and appropriate documentation of demanding physicochemical and biochemical analysis and preparation of analytical documentation in order to provide timely and quality analytical support for the smooth running of production processes. Acting in accordance with the law, internal regulations, Good Practices, and business objectives.
Key Responsibilities:
• Review, verification and approval of laboratory records and results.
• Ensure all activities in compliance with cGxP, and with data integrity. Perform Quality Control (QC) oversight activities.
• Manage OOx / analytical deviations and complaints and defining Corrective and Preventive Actions (CAPA).
• Participation in all training relevant to the position, maintenance of the relevant training evidence.
• Participation in inspections (interpretation of primary data and working method).
• Other tasks as assigned by the supervisor, and tasks based on a specific appointment.
Diversity & Inclusion / EEO
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
Essential Requirements:
• University degree in pharmacy, chemistry, biology or other equivalent natural science degree is preffered
• Preffered working experience. In case of Secondary school degree, minimum 5 years of relevant working experience required.
• Basic knowledge of English.
• Active knowledge of Slovene.
• Knowledge of Microsoft Office.
Desirable Requirements:
• Desired knowledge of basic physical chemistry and HPLC analysis.
• Desired work experience in the field of quality, development, production or other relevant field.
We offer temporary employment, with 6 months of probation period.
You are kindly invited to submit your application in English language, including CV.
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 morehere: https://www.novartis.com/about/strategy/people-and-culture
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.
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
• University degree in pharmacy, chemistry, biology or other equivalent natural science degree is preffered
• Preffered working experience. In case of Secondary school degree, minimum 5 years of relevant working experience required.
• Basic knowledge of English.
• Active knowledge of Slovene.
• Knowledge of Microsoft Office.
Desirable Requirements:
• Desired knowledge of basic physical chemistry and HPLC analysis.
• Desired work experience in the field of quality, development, production or other relevant field.
We offer temporary employment, with 6 months of probation period.
You are kindly invited to submit your application in English language, including CV.
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 morehere: https://www.novartis.com/about/strategy/people-and-culture
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.
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
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Operations
QUALITY
Slovenia
Menges
NVS Farmacevtska Proi. doo
Quality
Full Time
Temporary
Yes
