*Student Assistant in Project Management

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Studiejob - København

Would you like to work for a CDMO producing Active Pharmaceutical Ingredients (API) for different biopharmaceutical companies worldwide? Do you have an aspiration to become a project manager in a biopharmaceutical company? Do you have an interest in large-scale manufacturing of API using cell culture or microbial technology? And do you see yourself contributing to our continuous growth?

Then join AGC Biologics in a student assistant role and become part of an international and modern organization that delivers biopharmaceutical development and manufacturing.

Key Responsibilities

As a Student Assistant in the Project Management team you will be responsible for managing the calendar of client requests to schedule onsite, in-plant visits, coordinate logistics with the client and provide visibility to internal stakeholders and management. Additionally, you will be the main point of contact for the clients during their visits, and will be responsible for escorting onsite clients, ensuring clients have adequate work facilities, ensuring PiP (Person in Plant) adherence to company guidelines and site standards, helping coordinate and manage the clients' engagement with AGC staff and ensuring that there is no disruption to the ongoing site operations. You will work closely with the Project Management team to assist them in a number of tasks including scheduling of client meetings, customer shipments, scanning and archiving of documents or other tasks required by the Project Manager. AGC is a very dynamic and fast-moving company you will be exposed to many interesting Project Management related aspects and tasks. Furthermore, you will get great insight into the biopharmaceutical industry.

Who are we looking for:

You are diplomatic, detail-oriented, service-minded, and driven by the opportunity to provide first class support. You have a positive can-do attitude, as you will have to juggle the various demands of a fast-paced and versatile business environment. It is expected of you to work flexible working hours, on-call, if needed as the projects demands.

We expect you to have:

  • Bachelor's Degree
  • 3+ years' experience with MS Office and relevant Microsoft Technologies
  • Flexible, solution oriented approach
  • Are self-driven and with an ability to adapt to change quickly and comfortable dealing with ambiguity
  • Excellent communication skills
  • An ability to translate complex concepts into easily digestible written summaries
  • Professional appearance and can-do attitude. Positive demeanor.

We imagine that you are having a Bachelor’s degree, or being with the last year of a Bachelor’s study in Biotechnology, Chemical Engineering, or related studies.

We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible.

Application

We continuously evaluate incoming applications and conduct interviews accordingly. Therefore, please submit your application and CV as soon as possible. When the right candidate are found, the ad will close.

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 team

The open position is within a team supporting all the manufacturing departments with production. We work within cGMP and handle tasks related to creating and updating production documentation and supporting the production team. The team comprise of 16 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 position

As a scientist in the team, you will build competences to become a specialist in the portfolio of task related to production. You will be responsible for:

  • Creating production documentation
  • Handling deviations
  • Implementing improvements and handling Changes and CAPA’s
  • Training of manufacturing associates
  • Support to the manufacturing team
  • Participate in regulatory inspections and audits
  • Participate in board meetings, KPI delivery and follow-up
  • Optimization and standardization of work processes related to facility compliance

Experience and competencies

The ideal candidate have the right “can-do” mindset, is eager to learn and happy to work in a fast-paced environment. As a person you are driven by continuously improving processes and procedures. Experience with applied Lean is an advantage. Furthermore, you are curious, have a good overview, is eager to learn and is a team player. An academic degree within science, pharmacy or engineering forms the basis of the on-the-job training that will be provided.

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 "Projektleder", og befinder sig i kategorien "Ledelse og personale".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 30.6.2023, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Projektleder
  • København
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