Documentation Specialist Vaccines

What will your job be

As Documentation Specialist Vaccines you will be part of the Quality Assurance department to improve processes and focus on the customer. Key responsibilities:

• TruVault superuser; Process TruVault access requests, review/approve documentation and make documents effective in the system
• Summit superuser; process access requests, act as contact point, assign trainings, usergroups and curricula based on the required access
• TrackWise superuser; process access requests
  
• Represents the Docs&Data department in operational meetings when needed
  

What are we looking for

For this position as Documentation Specialist Vaccines we are looking for a motivated candidate with a relevant BSc in a scientific discipline, for example pharmacy or bio-pharmaceutical sciences. Furthermore you:

• Have 1-5 years of quality assurance/quality control experience in a pharmaceutical GMP setting, by preference vaccines
• Are used to work according to specific protocols and standards
• Have experience with review activities in a regulated environment is a plus
• Are independent and organized accurate worker, with eye for detail
• Are pro-active in the identification of issues, has problem-solving capabilities, and timely implements solutions
• Communicate effectively with professional staff and leadership across departments

What do we offer

• A contract starting for 12 months via CheckMark with the possibility of extension
  
• Salary range starts at €3139,- gross per month based on 40 hours/week
• Full-time position
  
• Dayshift

Where will you work

Our client is one of the biggest companies in health care, specialized in the development, production, and marketing of vaccines to prevent and combat infectious diseases. The Quality Assurane department is currently involved in for example COVID-19 vaccine development and is responsible for overseeing and supporting quality systems, projects and facilities.

More information

Ref.nr: 7455