Junior Consultant - Pharma

IQVIA; Kampenhout; Sur place; EUR 35 000 - 50 000; Plein temps

Avantages offerts par ce poste

Competitive salary and benefits

Development opportunities

Résumé du poste

IQVIA in Kampenhout is looking for a Junior Consultant to support senior colleagues with quality assurance, medical writing, and regulatory compliance tasks. This role offers you the opportunity to engage in various domains such as Pharmacovigilance and Quality Assurance, providing essential services within the pharmaceutical sector.

We offer a permanent full-time position with a competitive package, development opportunities, and a chance to work with a dynamic team on challenging projects.

Qualifications

• Master's degree in life sciences required.
• Good communication skills in Dutch, French, and English (verbal and written).
• Ability to problem-solve and show initiative.

Responsabilités

• Support more senior colleagues in ensuring product quality and safety.
• Assist in regulatory compliance for a range of products.
• Support the Quality Assurance (QA) processes and investigations.

Connaissances

Good knowledge of national and European regulations

Good communication skills in Dutch, French, and English

Strong initiative and problem-solver

Accurate & efficient

Good communicator & team player

Formation

Master’s degree in life sciences

Description du poste

Junior Consultant

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 of the client’s portfolio. This gives you the opportunity to acquire experience within one or several of the following domains:

Medical & Regulatory Affairs

• Medical writing: expert reports, clinical evaluations, literature study
• 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 check with applicable regulations
• Training of 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 (QA check, CoA request, artwork request, contact with warehouse/supply, …)
• Investigate customer complaints and non-conformance issues

Technical Skill Requirements

• Master degree in life sciences
• Good knowledge of national and European regulations and legislations for medicinal products
• Good communication skills in Dutch, French and English (both verbal and written)
• Strong initiative, problem solver and good organizational 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
• Challenging and alternating job as consultant within a dynamic team
• Development opportunities by working on various projects for different pharmaceutical companies

Our offices are located in Kampenhout at the business center “Hof ter Loonst”.