Why in2pharma

Who we are looking for…

We are a team of highly educated consultants, all holding at least a Master's degree, with a dynamic approach and a passion for problem solving.

We work as a team across Quality Assurance, Regulatory Affairs, Healthcare Compliance, Pharmacovigilance and Medical Affairs, from our offices in Kampenhout and Ghent or at our clients' sites across the Benelux.

Around since 2005

Part of IQVIA

Offices in Kampenhout & Ghent

Benelux coverage

Open positions

Our current vacancies

Junior Consultant

  • Kampenhout / Ghent
  • Full-time
  • Permanent contract

in2pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for the pharmaceutical and healthcare industry in the Benelux. We are looking for a Junior Consultant to join our team.

Main areas of responsibility

As a junior consultant at in2pharma, you will be trained to support more senior colleagues in ensuring the client’s products meet the required standards of quality and safety, and in ensuring regulatory compliance for a defined range of products in the client’s portfolio. This gives you the opportunity to gain experience in one or more of the following domains:

  • Medical & Regulatory Affairs
    • Medical writing: expert reports, clinical evaluations, literature studies
    • Medical education of sales representatives: product training on medicinal or healthcare products
    • Review and approve promotional material for medicinal and healthcare products
    • Adapt SPC, PIL and packaging materials in line with the registration file and legislation
  • Pharmacovigilance (PV)
    • Local literature review for adverse events on the MAH’s medicinal products
    • Assist in the PV quality system set-up or maintenance: PV SOPs, gap analysis, compliance checks against applicable regulations
    • Training of the MAH’s employees in PV awareness
  • Quality Assurance (QA)
    • Support the QP/RP in all aspects related to quality and compliance, ensuring local requirements are met
    • Support the QP/RP in the administrative release to the market in compliance with procedures, including QA check, CoA request, artwork request and contact with warehouse/supply
    • Investigate customer complaints and non-conformance issues

Technical skill requirements

  • Master’s degree in life sciences
  • Good knowledge of national and European regulations and legislation for medicinal products
  • Good communication skills in Dutch, French and English (verbal and written)
  • Strong initiative, problem solver, good organisational skills
  • Accurate & efficient: concern for quality, compliance and consistency
  • Good communicator & team player

Our offer

  • A permanent full-time position with a competitive package and supplementary benefits
  • A challenging and varied job as a consultant within a dynamic team
  • Development opportunities by working on various projects for different pharmaceutical companies

Do you want to join the in2pharma team? Send your CV and motivation to jobs@in2pharma.com.

Apply for this position
Spontaneous application

No matching vacancy?

We are also always open to a spontaneous application. Interested? Send your CV and cover letter to jobs@in2pharma.com.

Apply by email