Technician, QC Equipment
AGC Biologics
Dato: for 13 timer siden
By: København, Region Hovedstaden
Kontrakttype: Fuld tid
Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.
Are you looking for an exciting job in an expanding international company producing new biological medicines? Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team? We have the ideal opportunity for you! Quality Control (QC) at AGC Biologics is looking for a quality-minded Technician for our QC Equipment department!
The QC Organization
The QC organization consists of 160 dedicated colleagues, and we are responsible for supporting the production of new biopharmaceuticals by performing analytical testing of samples from the production and stability programs and validating various analytical procedures.
The QC Equipment Department owns all equipment in QC and is responsible for life cycle management activities such as procurement, installation/qualification, maintenance, (re)qualification/calibration, and decommissioning. All activities are performed in compliance with cGMP.
Role & Responsibilities
As Technician in QC Equipment, you will be responsible for ensuring that analytical instruments are being kept in compliance and in operational order to allow for our continuous analytical testing. The role includes, but is not limited to, the following responsibilities:
The ideal candidate holds a degree as laboratory technician (Laborant/Laboratorietekniker) or equivalent - and if you have a few years of experience working in a GMP laboratory, it is an advantage.
In addition, we are looking for the following professional skills...:
Apply today! We treat the applications as we receive them and conduct interviews with qualified candidates. When the right candidates are found, the add will close. For further information regarding the position, please contact Manager, Jesper Fuglsang Luxhøi, QC Equipment, by email: [email protected].
Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook!
AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.
Are you looking for an exciting job in an expanding international company producing new biological medicines? Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team? We have the ideal opportunity for you! Quality Control (QC) at AGC Biologics is looking for a quality-minded Technician for our QC Equipment department!
The QC Organization
The QC organization consists of 160 dedicated colleagues, and we are responsible for supporting the production of new biopharmaceuticals by performing analytical testing of samples from the production and stability programs and validating various analytical procedures.
The QC Equipment Department owns all equipment in QC and is responsible for life cycle management activities such as procurement, installation/qualification, maintenance, (re)qualification/calibration, and decommissioning. All activities are performed in compliance with cGMP.
Role & Responsibilities
As Technician in QC Equipment, you will be responsible for ensuring that analytical instruments are being kept in compliance and in operational order to allow for our continuous analytical testing. The role includes, but is not limited to, the following responsibilities:
- Performing maintenance of analytical instruments such as HPLCs, CEs, NIR, ELISA readers, SoloVPE, qPCR instruments etc.
- Maintaining other types of equipment like climate chambers, freezers, pipettes, balances etc.
- Working closely together with vendors.
- Working closely with other departments for systematic problem-solving and effective solution implementation.
- Maintaining assigned maintenance records, work orders, and service agreements in an orderly and accurate manner.
- Assisting in qualification activities.
- All work in the department is performed under cGMP and you will be responsible for finalizing service reports and enter work performed in the equipment database.
The ideal candidate holds a degree as laboratory technician (Laborant/Laboratorietekniker) or equivalent - and if you have a few years of experience working in a GMP laboratory, it is an advantage.
In addition, we are looking for the following professional skills...:
- (Technical) experience with life cycle management of analytical equipment such as HPLC, iCIEF, CE-SDS, ELISA readers, SoloVPE, and qPCR instruments
- Strong analytical and problem-solving skills and experience applying these skills to resolve technical problems.
- Experience to collaborate with vendors.
- Experience with working in cGMP settings according to European and US regulatory guidelines.
- and personal skills:
- Capacity to prioritize your own tasks in a dynamic environment.
- Good communication and interpersonal skills
- Ability to interact positively within a team and in close collaboration with other working areas when needed.
- It is important to have a self-motivating personality with a pragmatic attitude and approach to the daily work - without compromising quality.
- You thrive in a challenging and dynamic environment and enjoy a rapid pace of work.
- You bring a positive, can-do attitude and a good sense of humor.
Apply today! We treat the applications as we receive them and conduct interviews with qualified candidates. When the right candidates are found, the add will close. For further information regarding the position, please contact Manager, Jesper Fuglsang Luxhøi, QC Equipment, by email: [email protected].
Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook!
AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.
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