GMP professional

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

You will be joining a close knitted team and your tasks will include reviewing GMP-documentation, supporting daily operations, and participate in projects focused to optimize the production flow.

Team responsibilities and ambitions
The core task for our team is to review and ensure the integrity of batch documentation whilst supporting the production. The team ensures that the production is performed and documented according to GMP regulations and internal guidelines. Other tasks include failure investigation, initiation and investigation of deviations, and implementation of changes and corrective and preventative actions.

Alongside daily tasks you are expected to participate in both internal and external projects aimed to boost continuous improvement. You must have strong collaboration and communication skills as you will be collaborating with QA, Engineering Maintenance, and other departments.

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

• Review of batch documentation
• Support daily production
• Initiate deviations and perform root cause analysis
• Write, review, and approve GMP documentation
• Initiate problem-solving activities
• Participate in optimization activities on processes and equipment

Who are you?

We expect you to have an education as a cand.pharm or similar as well as general understanding of GMP production and documentation. We expect that you have a proactive, thorough, and analytical approach to problem solving. Furthermore, you must be fluent in written and oral Danish and English.

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

• Experience with GMP
• Experience with documentation
• Experience with production equipment
• Good people skills

We offer
An exciting and challenging job in a company with high 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 on +45 61816700 or [email protected]

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

You will be joining a close knitted team and your tasks will include reviewing GMP-documentation, supporting daily operations, and participate in projects focused to optimize the production flow.

Team responsibilities and ambitions
The core task for our team is to review and ensure the integrity of batch documentation whilst supporting the production. The team ensures that the production is performed and documented according to GMP regulations and internal guidelines. Other tasks include failure investigation, initiation and investigation of deviations, and implementation of changes and corrective and preventative actions.

Alongside daily tasks you are expected to participate in both internal and external projects aimed to boost continuous improvement. You must have strong collaboration and communication skills as you will be collaborating with QA, Engineering Maintenance, and other departments.

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

• Review of batch documentation
• Support daily production
• Initiate deviations and perform root cause analysis
• Write, review, and approve GMP documentation
• Initiate problem-solving activities
• Participate in optimization activities on processes and equipment

Who are you?

We expect you to have an education as a cand.pharm or similar as well as general understanding of GMP production and documentation. We expect that you have a proactive, thorough, and analytical approach to problem solving. Furthermore, you must be fluent in written and oral Danish and English.

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

• Experience with GMP
• Experience with documentation
• Experience with production equipment
• Good people skills

We offer
An exciting and challenging job in a company with high 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 on +45 61816700 or [email protected]

Department: Artillerivej 5, København S