Senior QA Professional for small molecules, Emerging Technologies
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Are you passionate about setting direction within emerging technologies and ensuring compliance? Are you motivated by navigating complex stakeholder landscapes and motivating teams to deliver great results? Do you thrive in a constantly changing environment with various challenges and growth opportunities to handle?
If so, we have an exciting opportunity for you, apply now!
The Position
As a Senior QA professional in our Emerging Technologies QA team for Manufacturing Development, you will play a critical role in ensuring the quality and compliance of our novel manufacturing methods, products, and technologies. is expanding within small molecules and in this position, you will primarily work with small molecules from Contract Manufacturing Organizations (CMO). Your responsibilities will include reviewing and approving documents related to stability, process validations, and product specifications for oral drug products and active pharmaceutical ingredient products.
In addition to these core responsibilities, you will also be responsible for leading complex cases with a high level of attention and driving innovation projects with stakeholders both locally and internationally. As a key member of our QA team, you will help set the quality direction and ensure alignment across the organization. Your focus will be on influencing and setting the right level of compliance, optimizing processes through a LEAN mindset, and establishing new processes that support our business objectives.
This position will be situated in Taastrup from September 2024, and the office presence is expected at minimum three days weekly.
Qualifications
The ideal candidate has several years of QA experience and has worked with small molecules and API/solid dosage forms (tablets) in a GMP environment. To succed in this role, you: Hold a MSc in Pharmacy, Engineering, Biology, Chemistry or similar Have several years of prove experience in QA or production role within the pharmaceutical industry Have excellent communication and interpersonal skills Can work collaboratively in a team environment while challenging the status quo Are fluent in both English and Danish
It will be seen as an advantage if you have experience with CMOs. The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural urge to handle quality issues at the right level, make decisions and follow-up on quality related problems. You are a self-motivated and independent person with a high level of responsibility and initiative who can prioritize your various tasks. You enjoy working in a dynamic environment, where teamwork is essential, and you like collaborating with many different stakeholders – internally and externally.
About the department
Emerging Technologies QA is a new area within where the oral portfolio plays a significant role. Emerging Technologies QA has approximately 100 employees and we are growing. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets and future emerging technologies products for the market. We are proud to work in a fast-growing part of .
You will become part of a great QA department (Emerging Technologies QA New Entry & Support), with many interfaces around the organization. The department consists of around 30 people divided into four teams, and this position is in the QA for Manufacturing Development team. The team consists of 9 highly knowledgeable and skilled people, covering the diverse area of Manufacturing Development.
In the department, we take great pride in our work and value challenges as opportunities. We have a vibrant and positive working environment, good values and exchange of knowledge and experience. We all work towards continuously improving our competences, as well as making work processes more efficient and effective.
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
For further information, please contact Associate Manager Maja Gro Rydahl +.
Deadline
9 April 2024
Applications will be evaluated continuously when received, and candidates may be called for interview before the deadline. 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 or 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 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.
If so, we have an exciting opportunity for you, apply now!
The Position
As a Senior QA professional in our Emerging Technologies QA team for Manufacturing Development, you will play a critical role in ensuring the quality and compliance of our novel manufacturing methods, products, and technologies. is expanding within small molecules and in this position, you will primarily work with small molecules from Contract Manufacturing Organizations (CMO). Your responsibilities will include reviewing and approving documents related to stability, process validations, and product specifications for oral drug products and active pharmaceutical ingredient products.
In addition to these core responsibilities, you will also be responsible for leading complex cases with a high level of attention and driving innovation projects with stakeholders both locally and internationally. As a key member of our QA team, you will help set the quality direction and ensure alignment across the organization. Your focus will be on influencing and setting the right level of compliance, optimizing processes through a LEAN mindset, and establishing new processes that support our business objectives.
This position will be situated in Taastrup from September 2024, and the office presence is expected at minimum three days weekly.
Qualifications
The ideal candidate has several years of QA experience and has worked with small molecules and API/solid dosage forms (tablets) in a GMP environment. To succed in this role, you:
About the department
Emerging Technologies QA is a new area within where the oral portfolio plays a significant role. Emerging Technologies QA has approximately 100 employees and we are growing. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets and future emerging technologies products for the market. We are proud to work in a fast-growing part of .
You will become part of a great QA department (Emerging Technologies QA New Entry & Support), with many interfaces around the organization. The department consists of around 30 people divided into four teams, and this position is in the QA for Manufacturing Development team. The team consists of 9 highly knowledgeable and skilled people, covering the diverse area of Manufacturing Development.
In the department, we take great pride in our work and value challenges as opportunities. We have a vibrant and positive working environment, good values and exchange of knowledge and experience. We all work towards continuously improving our competences, as well as making work processes more efficient and effective.
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
For further information, please contact Associate Manager Maja Gro Rydahl +.
Deadline
9 April 2024
Applications will be evaluated continuously when received, and candidates may be called for interview before the deadline. 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 or 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 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 Måløv.
Jobbet er oprettet på vores service den 15.3.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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