Senior QA Technician

Are you an experienced Laboratory Technician or Technician with a strong background in aseptic production? We are looking for a Senior QA Technician to join our team at [xxxxx]. If you are ready for the next step in your career, read on and apply today for a life-changing opportunity. The position As a Senior QA Technician, you will be part of an operation team which mainly consist of QA delegates (releasing QA’s). Our team handle a high level of complexity in our daily tasks as we are responsible for approval of documentations from of contract manufacturing for aseptic contract manufactures (CMO’s) producing drug products. In this role you can expect that you will be responsible for:

Reviewing CMO documentation for batch production at CMO

Approving deviations from CMOs and/or [xxxxx] deviations

Coordinate and collecting documentation for annual product reviews (APR), batch release etc.

Making independent decisions and driving quality improvements

Please be aware that the position is currently in Søborg, but it will be moving to new office buildings in Taastrup by the end of 2024. Since the manufacturers are located outside Denmark, you are expected to travel 5-10 days a year. Qualifications To be successful in this role, we are looking for candidates with the following qualifications:

Several years of experience working as a Laboratory Technician or Technician in an aseptic production and/or QA

Knowledge of quality assurance processes and standards

Familiarity with regulatory requirements and compliance

Proficiency in English, both written and verbally

As a person, you have a strong attention to detail and the ability to make independent decisions. You are proactive and possess driven mindset with a focus on finding solutions. You have excellent communication and interpersonal skills as well as ability to work effectively in a team and collaborate with cross-functional stakeholders. About the department Global Contract Manufacturing (GCM) QA is a dynamic department consisting of 50 competent people and is characterized by a high level of professionalism, flexibility, and collaboration. GCM is an inclusive and international business environment. The primary role of our department is to deliver QA support and set direction for our Global Contract Manufacturer Organizations worldwide. The open position as QA Professional is in the GCM QA Operations Drug Product Aseptic team, which is responsible for aseptic production at the CMO´s. Working at [xxxxx] At [xxxxx], 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 For further information about the position, please contact Linea Frenk Alsing, Manager, via phone +[xxxxx]or email [xxxxx] . Deadline June 23, 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 CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. Are you an experienced Laboratory Technician or Technician with a strong background in aseptic production? We are looking for a Senior QA Technician to join our team at [xxxxx]. If you are ready for the next step in your career, read on and apply today for a life-changing opportunity. The position As a Senior QA Technician, you will be part of an operation team which mainly consist of QA delegates (releasing QA’s). Our team handle a high level of complexity in our daily tasks as we are responsible for approval of documentations from of contract manufacturing for aseptic contract manufactures (CMO’s) producing drug products. In this role you can expect that you will be responsible for:

Reviewing CMO documentation for batch production at CMO

Approving deviations from CMOs and/or [xxxxx] deviations

Coordinate and collecting documentation for annual product reviews (APR), batch release etc.

Making independent decisions and driving quality improvements

Please be aware that the position is currently in Søborg, but it will be moving to new office buildings in Taastrup by the end of 2024. Since the manufacturers are located outside Denmark, you are expected to travel 5-10 days a year. Qualifications To be successful in this role, we are looking for candidates with the following qualifications:

Several years of experience working as a Laboratory Technician or Technician in an aseptic production and/or QA

Knowledge of quality assurance processes and standards

Familiarity with regulatory requirements and compliance

Proficiency in English, both written and verbally

As a person, you have a strong attention to detail and the ability to make independent decisions. You are proactive and possess driven mindset with a focus on finding solutions. You have excellent communication and interpersonal skills as well as ability to work effectively in a team and collaborate with cross-functional stakeholders. About the department Global Contract Manufacturing (GCM) QA is a dynamic department consisting of 50 competent people and is characterized by a high level of professionalism, flexibility, and collaboration. GCM is an inclusive and international business environment. The primary role of our department is to deliver QA support and set direction for our Global Contract Manufacturer Organizations worldwide. The open position as QA Professional is in the GCM QA Operations Drug Product Aseptic team, which is responsible for aseptic production at the CMO´s. Working at [xxxxx] At [xxxxx], 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 For further information about the position, please contact Linea Frenk Alsing, Manager, via phone +[xxxxx]or email [xxxxx] . Deadline June 23, 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 CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At [xxxxx] 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.