Global Regulatory Affairs Specialist - Full Lifecycle

Interchemie; Waalre; On-site; EUR 41,000 - 49,000; Full time

Benefits offered by this job

Salary up to €4,000 gross per month

International working environment

Close collaboration with QA, QC,物流 and

Job summary

Interchemie in Waalre, Netherlands, seeks a Regulatory Affairs Specialist to manage regulatory dossiers from A to Z across international markets. English is the working language in the RA team, and you will collaborate daily with QA, QC, logistics and sales to ensure registrations move smoothly from submission to market release.

A one-hour commute to Waalre is expected. With 1 to 3 years of experience in a regulated life sciences environment, you will own ownership, accuracy and structured

Qualifications

• Master’s degree in Life Sciences.
• 1–3 years of relevant Regulatory Affairs experience.
• Fluency in English; Dutch not required.

Responsibilities

• Prepare, compile and submit regulatory dossiers for new registrations across international markets.
• Manage the full lifecycle of regulatory dossiers including variations and renewals.
• Take ownership of a portfolio of countries and ensure registrations remain compliant and up to date.
• Collaborate with QA, QC, logistics and sales to ensure registrations, release and supply to the market.

Skills

Regulatory affairs experience

English fluency

Russian language (nice to have)

Education

Master’s degree in Life Sciences

Job description

Interchemie in Waalre, Netherlands, seeks a Regulatory Affairs Specialist to manage regulatory dossiers from A to Z across international markets. English is the working language in the RA team, and you will collaborate daily with QA, QC, logistics and sales to ensure registrations move smoothly from submission to market release.

A one-hour commute to Waalre is expected. With 1 to 3 years of experience in a regulated life sciences environment, you will own ownership, accuracy and structured