QC Technician for QC Raw Materials Team
at AGC Biologics
København, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 25 Oct, 2024 | Not Specified | 28 Jul, 2024 | N/A | Addition,English | No | No |
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Description:
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.
The Position
You will be a part of the QC Raw Materials Team which, together with the QC Stability and the QC Samples and Service teams, make up QC Support.
Your working day is characterized by a mix between sampling Raw Materials, working at your desk, and analyzing Raw materials. In this role you can expect ongoing collaboration with the QC Raw materials scientists as well as technicians.
Your responsibilities involve:
- Preparing and performing sampling of Raw Materials
- Handling of sample shipments
- Engaging with internal and external stakeholders
- Analysis of Raw materials using NIR and appearance
- Ensuring compliance to GMP and relevant SOP’s
The Department
You will be part of QC Raw Materials within QC Support where you will join a team of highly dedicated scientists and technicians.
QC Support consists of three departments: QC Raw materials, QC Samples & Service and QC Stability. QC Stability is comprised of 6 Scientists and 4 technicians.
The Profile
The ideal candidate has an education as a Laboratory technician or other relevant degree and preferably with work experience within quality control
In addition, we expect you to bring some of the following experience and characteristics
- Experience with working in a GMP Laboratory
- Knowledgeable in sampling and material handling
- Knowledge of NIR
- The ability to communicate clearly in English
- You are a team player combined with the ability and desire to work independently
Furthermore, 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.
Interested?
Send your application as soon as possible. We treat the applications as we receive them, and conduct interviews with qualified applicants before the deadline. If you need further information about the position, please feel free to contact Stella Brudin, Manager of QC Raw Materials at +45 27 60 24 73
We look forward to hearing from you.
Want to keep posted about our growth and to learn more about our company?
We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !
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
Responsibilities:
- Preparing and performing sampling of Raw Materials
- Handling of sample shipments
- Engaging with internal and external stakeholders
- Analysis of Raw materials using NIR and appearance
- Ensuring compliance to GMP and relevant SOP’
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
København, Denmark