Junior Consultant - Pharma

IQVIA; Kampenhout; On-site; EUR 38,000 - 55,000; Full time

Benefits offered by this job

Permanent full-time position

Development opportunities

Job summary

IN2Pharma is seeking a Junior Consultant to join our team in Belgium. You will contribute to Medical & Regulatory Affairs, Pharmacovigilance and Quality Assurance across projects for pharmaceutical clients.

The role involves medical writing, training of sales staff, review of promotional material and ensuring compliance with national and European regulations. Office locations include Kampenhout and Gentbrugge, offering a dynamic consultancy environment.

Qualifications

• Master's degree in life sciences is required.
• Good knowledge of national and European regulations for medicinal products.
• Excellent written and spoken Dutch, French and English.
• Strong initiative, problem solving and organizational skills.
• Accurate and efficient with a focus on quality and compliance.
• Excellent communicator and team player.

Responsibilities

• Medical writing: expert reports, clinical evaluations and 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 to registration files and legislation.
• Local literature review for adverse events on MAH's medicinal products (PV).
• Assist in PV quality system set-up or maintenance: PV SOPs, gap analysis, compliance checks.

Skills

Communication skills

Initiative

Organizational skills

Team player

Accuracy & efficiency

Education

Master's degree in life sciences

Job description

We are looking for a Junior Consultant to join our team.

Main Areas of Responsibility

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. This includes: 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

IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for pharmaceutical and healthcare industry in Benelux.

Our offices are located in Kampenhout at the business center "Hof ter Loonst" and in Gentbrugge.