QA Professional
Kalundborg
Do you like to have an impact on decisions? Are you able to ensure compliance and high quality in your job? Would you thrive by working with skilled colleagues known for their fantastic team spirit? If so then work with us in Kalundborg.
Apply now and join us!
The position
In close cooperation with colleagues, you will act as a QA Professional in Aseptic Manufacturing Kalundborg. Ensuring that our products are of high standards and in full compliance with the current rules and guidelines. We are offering an exciting and flexible job where you will be part of a competent and well-functioning team.
Your main responsibilities will be within some of the following tasks:
• Review and approval of batch documentation, batch-related documentation from support processes, trend reports, Standard Operating Procedures (SOPs) and deviations.
• Perform QA oversight, observing the performance of processes and helping solve issues in real-time.
• Advising stakeholders to ensure the right level of quality in the production processes.
• Participating and presenting cases when we are inspected by authorities from around the world.
• Improve processes in your working area.
Qualifications
To succeed in this role you should have:
• A Master’s degree in pharmacy, medicine, microbiology, veterinary medicine or similar.
• Experience within QA and other relevant production related job would be advantageous.
• Knowledge of Good Manufacturing Practice (GMP) and regulations.
• Strong communication skills with stakeholders, maintaining a respectful tone.
• Proficiency in English
As a person, you possess a keen eye for detail and are naturally engaged. You excel in establishing strong relations with stakeholders, making you an asset to our team both personally and professionally.
About the department
Aseptic Manufacturing in Kalundborg is a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We are 60 engaged employees with great team spirit, and we overcome obstacles with open and honest communication. We love professional challenges, working with individual responsibilities, and is one of the best places to work and grow.
Our main task is to help set and ensure the quality direction of our production area, thereby having direct impact on products delivered to patients all over the world. Meaning, our QA role is to advice and confirm to ensure our production is in compliance with internal and external guidelines at all times.
Working at
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
If you have any questions, you are welcome to contact Manager Rie Nielsen on +.
Deadline
28 July 2024
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume / CV. We will review applications received on an ongoing basis, so do not hesitate to apply as soon as possible.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Apply now and join us!
The position
In close cooperation with colleagues, you will act as a QA Professional in Aseptic Manufacturing Kalundborg. Ensuring that our products are of high standards and in full compliance with the current rules and guidelines. We are offering an exciting and flexible job where you will be part of a competent and well-functioning team.
Your main responsibilities will be within some of the following tasks:
• Review and approval of batch documentation, batch-related documentation from support processes, trend reports, Standard Operating Procedures (SOPs) and deviations.
• Perform QA oversight, observing the performance of processes and helping solve issues in real-time.
• Advising stakeholders to ensure the right level of quality in the production processes.
• Participating and presenting cases when we are inspected by authorities from around the world.
• Improve processes in your working area.
Qualifications
To succeed in this role you should have:
• A Master’s degree in pharmacy, medicine, microbiology, veterinary medicine or similar.
• Experience within QA and other relevant production related job would be advantageous.
• Knowledge of Good Manufacturing Practice (GMP) and regulations.
• Strong communication skills with stakeholders, maintaining a respectful tone.
• Proficiency in English
As a person, you possess a keen eye for detail and are naturally engaged. You excel in establishing strong relations with stakeholders, making you an asset to our team both personally and professionally.
About the department
Aseptic Manufacturing in Kalundborg is a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We are 60 engaged employees with great team spirit, and we overcome obstacles with open and honest communication. We love professional challenges, working with individual responsibilities, and is one of the best places to work and grow.
Our main task is to help set and ensure the quality direction of our production area, thereby having direct impact on products delivered to patients all over the world. Meaning, our QA role is to advice and confirm to ensure our production is in compliance with internal and external guidelines at all times.
Working at
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
If you have any questions, you are welcome to contact Manager Rie Nielsen on +.
Deadline
28 July 2024
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume / CV. We will review applications received on an ongoing basis, so do not hesitate to apply as soon as possible.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Kalundborg.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Kalundborg