Global Regulatory Affairs Specialist - Chemistry Focus

B-Hive Switzerland; Basel; On-site; CHF 90,000 - 130,000; Full time

Benefits offered by this job

Close-knit team

Engineering expertise

Training opportunities

Career growth

Job summary

B-Hive Switzerland is seeking a Chemist Regulatory Affairs Specialist to join a major project with a client in Switzerland. You will support regulatory documentation and certificates across countries, contributing to global regulatory activities.

You bring a technical or scientific background, hands-on experience in product registration or regulatory docs, and strong MS Office/data management skills. Fluent English and good communication are essential, with a proactive, team-oriented mindset.

Qualifications

• Technical or scientific education related to regulatory affairs.
• First experience in product registration or regulatory documentation.
• Good command of MS Office and data management, along with project management skills.
• Experience in a chemical environment (asset).
• Fluent English; additional languages are a plus.
• Strong communication skills, good organizational sense and motivation.

Responsibilities

• Support supply chain management during the upcoming change of supply sites.
• Support the Global Regulatory team in day-to-day regulatory activities.
• Prepare and provide regulatory certificates for requests from various countries.
• Help resolve certificate and documentation issues worldwide.
• Issue letters of access for Marketing teams, Regulatory teams and third parties.
• Contribute to document management alongside global regulatory specialists.
• Provide operational support to all members of the department.

Skills

Regulatory affairs

English fluency

Communication skills

Project management

Education

Technical or scientific education related to regulatory affairs

Tools

MS Office

Data management

Job description

B-Hive Switzerland is seeking a Chemist Regulatory Affairs Specialist to join a major project with a client in Switzerland. You will support regulatory documentation and certificates across countries, contributing to global regulatory activities.

You bring a technical or scientific background, hands-on experience in product registration or regulatory docs, and strong MS Office/data management skills. Fluent English and good communication are essential, with a proactive, team-oriented mindset.