Global Scientific Affairs Manager (Hybrid – Remote)

SuperMicrobiologists; Germany (OH); Remote; USD 90,000 - 130,000; Full time

Job summary

SuperMicrobiologists is seeking a Global Scientific Affairs Manager to develop and implement global strategies for method certification and product development. The ideal candidate will have a Master's or Ph.D. in a relevant field along with at least 5 years of experience in scientific or regulatory affairs. Responsibilities include engaging with regulatory authorities and providing support for validation acceptance. This hybrid role demands exceptional communication skills and the ability to navigate complex scientific data.

Qualifications

• Minimum 5 years of experience in scientific affairs, regulatory affairs, or method validation in food safety or analytical testing.
• Exceptional written and verbal communication skills with a proven ability to engage technical audiences.
• Highly self-motivated and adaptable in a fast-paced organization.

Responsibilities

• Develop and deploy global strategies for method certification and recognition.
• Build and maintain relationships with regulatory authorities.
• Provide scientific evidence and regulatory support for validation acceptance.

Skills

Deep knowledge of ISO 16140

Strong capability in translating complex scientific data

Strong networking skills

Exceptional written and verbal communication skills

Demonstrated strategic thinking

Education

Master's or Ph.D. in Microbiology, Food Science, Analytical Sciences, Biotechnology, or related field

Job description

Global Scientific Affairs Manager (Hybrid – Remote)

YOUR TASKS – BECOME A GAME CHANGER

• Develop and deploy global strategies for method certification and recognition for new product development, product improvement, modification, and scope extension.
• Define method application scopes and study designs in accordance with standards, guidance documents, and applicable technical regulations.
• Develop and ensure procedures for validation approvals to support and improve Hygiena's Product Commercialization Process (PCP).
• Build and maintain relationships with regulatory authorities; act as liaison between Hygiena, regulatory agencies, and industry partners.
• Provide scientific evidence and regulatory support to promote validation acceptance in national regulations and customer facilities.
• Represent Hygiena in scientific committees, standardization working groups, and regulatory meetings; present at industry conferences; engage with AOAC International, ISO, and national committees.
• Monitor regulatory trends, developments, and emerging scientific needs.

YOUR PROFIL – WHAT MAKES YOU SPECIAL

• Master's or Ph.D. in Microbiology, Food Science, Analytical Sciences, Biotechnology, or related field.
• Minimum 5 years of experience in scientific affairs, regulatory affairs, or method validation in food safety, water microbiology, or analytical testing industries.
• Deep knowledge of ISO 16140, AOAC validation studies, food safety and quality regulations.
• Strong capability in translating complex scientific data.
• Strong networking, stakeholder engagement, and relationship‑building skills.
• Exceptional written and verbal communication skills with a proven ability to engage technical audiences.
• Demonstrated strategic thinking, analytical capabilities, and problem‑solving skills.
• Highly self‑motivated and adaptable in a fast‑paced, matrixed organization.
• Excellent verbal and written communication in English.
• Able to travel up to 30%.