QC Specialist (m/f/d)

About the role

Location: Mengeš #LI-Onsite

As a QC Specialist (m/f/d), you will be responsibile for professional work in the analytics domain in order to ensure regulatory compliance and quality of processes and products in accordance with the law, internal regulations, good practices and business objectives.

Key Responsibilities:
• Manage OOx / analytical deviations and complaints.
• Ensure all activities in compliance with cGxP, and with data integrity. Perform Quality Control (QC) oversight activities.
• Review and approval of analytical tests (analytical release), materials and product.
• Support Implement of new methods and techniques.
• Participation within the validation, transfer and management of issues related to analytical methods and techniques in accordance with requirements.
• Support laboratory associates in their daily tasks and troubleshooting.
• Participation in all training relevant to the position, maintenance of the relevant training evidence.
• Other tasks as assigned by the supervisor, and tasks based on a specific appointment.

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Role Requirements

Essential Requirements:
• University degree in pharmacy, chemistry or any other natural science degree
• Functional knowledge of English and local language.
• Knowledge of Microsoft Office.
• Preferred working experience in the field of quality, development, manufacture, or other relevant field.

We offer permanent employment with 6 month 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, 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

About the role

Location: Mengeš #LI-Onsite

As a QC Specialist (m/f/d), you will be responsibile for professional work in the analytics domain in order to ensure regulatory compliance and quality of processes and products in accordance with the law, internal regulations, good practices and business objectives.

Key Responsibilities:
• Manage OOx / analytical deviations and complaints.
• Ensure all activities in compliance with cGxP, and with data integrity. Perform Quality Control (QC) oversight activities.
• Review and approval of analytical tests (analytical release), materials and product.
• Support Implement of new methods and techniques.
• Participation within the validation, transfer and management of issues related to analytical methods and techniques in accordance with requirements.
• Support laboratory associates in their daily tasks and troubleshooting.
• Participation in all training relevant to the position, maintenance of the relevant training evidence.
• Other tasks as assigned by the supervisor, and tasks based on a specific appointment.

{#400,300#}#/video#]

Role Requirements

Essential Requirements:
• University degree in pharmacy, chemistry or any other natural science degree
• Functional knowledge of English and local language.
• Knowledge of Microsoft Office.
• Preferred working experience in the field of quality, development, manufacture, or other relevant field.

We offer permanent employment with 6 month 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, 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

About the role

Location: Mengeš #LI-Onsite

As a QC Specialist (m/f/d), you will be responsibile for professional work in the analytics domain in order to ensure regulatory compliance and quality of processes and products in accordance with the law, internal regulations, good practices and business objectives.

Key Responsibilities:
• Manage OOx / analytical deviations and complaints.
• Ensure all activities in compliance with cGxP, and with data integrity. Perform Quality Control (QC) oversight activities.
• Review and approval of analytical tests (analytical release), materials and product.
• Support Implement of new methods and techniques.
• Participation within the validation, transfer and management of issues related to analytical methods and techniques in accordance with requirements.
• Support laboratory associates in their daily tasks and troubleshooting.
• Participation in all training relevant to the position, maintenance of the relevant training evidence.
• Other tasks as assigned by the supervisor, and tasks based on a specific appointment.

{#400,300#}#/video#]

Role Requirements

Essential Requirements:
• University degree in pharmacy, chemistry or any other natural science degree
• Functional knowledge of English and local language.
• Knowledge of Microsoft Office.
• Preferred working experience in the field of quality, development, manufacture, or other relevant field.

We offer permanent employment with 6 month 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, 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

Share

About the role

Location: Mengeš #LI-Onsite

As a QC Specialist (m/f/d), you will be responsibile for professional work in the analytics domain in order to ensure regulatory compliance and quality of processes and products in accordance with the law, internal regulations, good practices and business objectives.

Key Responsibilities:
• Manage OOx / analytical deviations and complaints.
• Ensure all activities in compliance with cGxP, and with data integrity. Perform Quality Control (QC) oversight activities.
• Review and approval of analytical tests (analytical release), materials and product.
• Support Implement of new methods and techniques.
• Participation within the validation, transfer and management of issues related to analytical methods and techniques in accordance with requirements.
• Support laboratory associates in their daily tasks and troubleshooting.
• Participation in all training relevant to the position, maintenance of the relevant training evidence.
• Other tasks as assigned by the supervisor, and tasks based on a specific appointment.

{#400,300#}#/video#]

Role Requirements

Essential Requirements:
• University degree in pharmacy, chemistry or any other natural science degree
• Functional knowledge of English and local language.
• Knowledge of Microsoft Office.
• Preferred working experience in the field of quality, development, manufacture, or other relevant field.

We offer permanent employment with 6 month 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, 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

389984BR

Slovenia

About the role

Location: Mengeš #LI-Onsite

As a QC Specialist (m/f/d), you will be responsibile for professional work in the analytics domain in order to ensure regulatory compliance and quality of processes and products in accordance with the law, internal regulations, good practices and business objectives.

Key Responsibilities:
• Manage OOx / analytical deviations and complaints.
• Ensure all activities in compliance with cGxP, and with data integrity. Perform Quality Control (QC) oversight activities.
• Review and approval of analytical tests (analytical release), materials and product.
• Support Implement of new methods and techniques.
• Participation within the validation, transfer and management of issues related to analytical methods and techniques in accordance with requirements.
• Support laboratory associates in their daily tasks and troubleshooting.
• Participation in all training relevant to the position, maintenance of the relevant training evidence.
• Other tasks as assigned by the supervisor, and tasks based on a specific appointment.

{#400,300#}#/video#]

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.

Role Requirements

Essential Requirements:
• University degree in pharmacy, chemistry or any other natural science degree
• Functional knowledge of English and local language.
• Knowledge of Microsoft Office.
• Preferred working experience in the field of quality, development, manufacture, or other relevant field.

We offer permanent employment with 6 month 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, 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

Division

Operations

Business Unit

QUALITY

Work Location

Menges

Company/Legal Entity

NVS Farmacevtska Proi. doo

Functional Area

Quality

Job Type

Full Time

Employment Type

Regular

Shift Work

No

Early Talent

Yes

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• Русский
• English (United States)
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• 日本語
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