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With AGC Biologics' increasing activities, we are looking for new scientists with experience preferably within API production or other areas within the pharmaceutical industry.
AGC Biologics is a Contract Manufacturing Organization (CDMO) with facilities in Denmark, Germany, Japan and USA and with customers from all over the world. We have more than 30 nationalities employed and the daily language is English.
The Adjuvant Support Team
The Adjuvant Support team is supporting the Adjuvant manufacturing with task related to ensuring compliance in the Adjuvant Manufacturing Team.
Our newly established team comprise of 9 engaged colleagues that are driven by the ever-changing manufacturing pace. We strive to ensure a high quality mindset and enjoy a great team spirit.
The team operates under cGMP and are responsible for continuous support to our dedicated adjuvant manufacturing line. The production consist of various unit operations such as buffer preparation, homogenization, filtration, tangential flow filtrations and filling operations. We securing the compliance framework around the department, covering daily documentation of the operations, establishment and maintenance of SOP’s, training documentation, deviations and CAPA management.
The position
As a manufacturing scientist in the Adjuvant Support team, you will become a process specialist on the adjuvant process. You will be responsible for:
- Write and review deviations, CAPA’s and change requests
- Secure training manufacturing associates
- Approve batch documentation and prepare for batch release
- cGMP compliance, training of manufacturing associates and a safe work environment
- Support the team preparing for regulatory inspections and audits
- Participate in board meetings, KPI delivery and follow-up
- Optimization and standardization of work processes.
Experience and competencies
The ideal candidate holds an Academic degree within science and have previously been working in a manufacturing team operating under cGMP preferably within the pharmaceutical industry. The ideal candidate for the position has several of the below competencies/experiences:
- 2+ years of experience from the pharmaceutical industry working in an cGMP environment
- Strong communication skills (English)
- Structured and analytically oriented
- Experience with applied Lean
- A genuine interest in being close to the manufacturing floor and understanding the need for process confirmation
As a person you are curious, have a good overview, is eager to learn and a team player: You thrive in a high pace environment where no two days are the same.
AGC Biologics offers
AGC Biologics offers a dynamic working place with good opportunities for 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.
For further information, please contact Anna Jaroszewski, Manager, Adjuvant Support, phone +45 27602427.
We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible and no later than February 20th, 2022.
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.
Information og data
Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 3.2.2022, men kan have været deaktiveret og genaktiveret igen.
- Forsker
- København
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