What are the responsibilities and job description for the Technician Mammalian Manufacturing position at AGC Biologics A/S?
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.
Technician for Mammalian Production coordination.
Join a dynamic and international company where everyone is responsible for delivering right on time as one team!
At AGC Biologics A/S (AGC), we develop biopharmaceutical processes and run GMP production of pharmaceutical proteins from early state test until commercial production. As we are a Contract Manufacturing Organization (CMO), the customer is in centrum, and we have a high level of service to our customers.
The department
As our new Technician in Mammalian Production Coordination Team, you will be part of a professional and dedicated Team consisting of both Scientists and Support technicians. You will experience a very dynamic working environment with a high variety of tasks, and an environment where cGMP production never becomes routine.
We work in close collaboration with other teams and departments who are dependent on the services we deliver.
Responsibilities and tasks
- MFG support
- Ensure that raw material and disposables is ready for production
- Collaboration with externals.
- Collaborate with planning.
- Participate in projects across Manufacturing
- Participate in LEAN projects across manufacturing
We are continuously working on improvements and optimization of existing processes and routines and support a strong learning environment where we within relatively short time become familiar with a variety of new processes and technologies.
Experience and competencies
You have GMP background, is a proactive team player, flexible and positive, and you:
- Can work according to written procedures in English
- Can work independently and with responsibility for own tasks.
- Can work in an organization with constant customer audits and inspections.
- Can work structured and have a sense of order.
As our corporate language is English, all our procedures and GMP related documents are in English. It is therefore important that you can read English without problems, and we also appreciate the ability to speak English at a certain level.
AGC Biologics offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges. This opens many doors for personal development and for you to make a real difference towards both patients and customer. At AGC Biologics, the work environment is informal, and humor is part of the work day. We respect each other and our differences, and we help each other to reach deadlines together as one team.
We will process the applications as they arrive. Therefore, please submit our resume and application as soon as possible.
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AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.
Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.
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.
