Team Lead Regulatory Affairs (Division Pharma) (m/f/d)

JR Germany; Ladenburg; Vor Ort; EUR 80.000 - 110.000; Vollzeit

Zusammenfassung

A leading company in the sustainable ingredients sector is seeking a Team Lead for Regulatory Affairs in Ladenburg. The role entails leading a team, ensuring compliance in product development, and engaging with internal and external stakeholders to drive regulatory projects. Candidates should have advanced degrees in relevant fields and significant experience in pharmaceutical regulatory affairs.

Leistungen

Competitive salary

Opportunities for professional growth

Collaborative work environment

Qualifikationen

• 3 years of professional experience in pharmaceutical regulatory affairs.
• 3 years of leadership experience.
• Fluent in German and English, both written and spoken.

Aufgaben

• Lead the Regulatory Affairs Team (Pharma).
• Act as a regulatory key/interface for stakeholders.
• Define and implement regulatory strategies.

Kenntnisse

Leadership

Stakeholder Engagement

Regulatory Compliance

Analytical Mindset

Communication Skills

Ausbildung

Master’s or PhD in food science, chemistry, chemical engineering

Jobbeschreibung

Team Lead Regulatory Affairs (Division Pharma) (m/f/d), Ladenburg

Client:

Location:

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

Posted:

22.06.2025

Expiry Date:

06.08.2025

Job Description:

Jungbunzlauer is a leading producer of high-quality, sustainable ingredients from natural sources, serving industries from food and beverage, nutrition, health, and home and personal care. Headquartered in Basel, Switzerland, with facilities across Europe and North America, we serve over 130 countries worldwide. Founded over 150 years ago, Jungbunzlauer has grown into a CHF 1.3 billion company, driven by nearly 1,400 colleagues committed to a healthier, more sustainable future.

Position: Team Lead Regulatory Affairs (Division Pharma) (m/f/d)

• Leadership: Lead the Regulatory Affairs Team (Pharma)
• Stakeholder Engagement: Act as a regulatory key/interface for internal and external stakeholders including partners, customers, and regulatory authorities (global)
• Project Coordination: Participate proactively in product development, launch, and market entry projects to ensure regulatory compliance
• Regulatory Strategy: Define, communicate, and implement clear regulatory strategies tailored to customer and country-specific requirements
• Documentation: Create and review product documentation, dossiers, and regulatory reports
• Digitalization: Develop and implement strategies for digitalization within regulatory affairs
• Audits: Support and accompany regulatory audits

Qualifications:

• Master’s or PhD in food science, chemistry, chemical engineering, or a comparable field
• At least 3 years of professional experience in pharmaceutical regulatory affairs
• At least 3 years of leadership experience
• Strong understanding of regulations, guidelines, and policies in the pharmaceutical sector
• Experience collaborating with authorities in the pharmaceutical industry
• Analytical mindset with creativity and intuition
• Ability to facilitate decision-making and organizational skills
• Excellent communication and interpersonal skills
• Fluent in German and English, both written and spoken

Additional benefits include a competitive salary, opportunities for professional growth, and a collaborative work environment. Please note that a valid work permit is required if you do not hold citizenship of the country where the job is located.