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GMP professional

AJ Vaccines


Are you keen to make a difference in your role and have strong problem-solving and communication skills? If so, AJ Vaccines is looking for a GMP Support Professional to join the Inspection & Packaging department.

As part of this role, you will primarily support daily production activities and review GMP documentation. You will work closely with a dedicated team to ensure that production runs smoothly and meets GMP regulations, while also participating in projects aimed at optimizing production flow.

Team Responsibilities and Ambitions

The core responsibility of our team is to review and ensure the integrity of batch documentation while supporting the production processes. We make sure that production is performed and documented according to GMP regulations and internal guidelines. Additionally, the team is involved in failure investigations, initiating and investigating deviations, and implementing changes, corrective actions, and preventative actions.

Alongside these daily tasks, you will also support the team in internal and external projects aimed at continuous improvement. Strong collaboration and communication skills are essential, as you will work closely with cross-functional teams such as QA, Engineering Maintenance, and other departments.

Your Work Tasks

Together with your team, you will be responsible for the following tasks:

  • Supporting daily production
    by troubleshooting issues and ensuring documentation aligns with GMP standards.
  • Reviewing batch documentation
    to maintain compliance and accuracy.
  • Initiating deviations
    and performing root cause analysis to resolve production issues.
  • Writing, reviewing, and approving
    GMP documentation.
  • Participating in optimization projects
    on processes and equipment.
  • Initiating problem-solving activities
    to ensure production flow remains efficient and smooth.

Who Are You?

We expect you to have an education such as cand.pharm or a similar qualification, along with a general understanding of GMP production and documentation. You should have a proactive, thorough, and analytical approach to problem-solving. Fluency in both written and oral Danish and English is essential for the role.

In addition, the following experience and skills are an advantage:

  • Experience with GMP.
  • Experience with documentation.
  • Experience with production equipment.
  • Strong people skills.

We Offer

An exciting and challenging job in a company with a high degree of professionalism, where you will work in a collaborative environment with a team of talented and experienced professionals. You will have the opportunity to take responsibility and grow your skills, making a positive impact on the company's operations and the lives of patients.

Interested?
Please submit your application online by uploading your CV. While a Cover Letter is not mandatory for this position, we encourage you to express your motivation in a few lines within your CV. As we are reviewing applications and conducting interviews continuously, we recommend applying at your earliest convenience.

At AJ Vaccines, we are committed to an inclusive recruitment process, ensuring equal opportunities for all applicants. Consequently, we kindly request that you refrain from including a photo in your CV.

If you have any questions or need further information, please contact Director Serkan Gokce at +45 61816700 or .

Department: Artillerivej 5, København S



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AJ Vaccines

Artillerivej 5, 2300 København S

AJ Vaccines is a global pharmaceutical company. We develop and manufacture vaccines against serious infectious diseases as well as diagnostic and therapeutic solutions.


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