Scientific Affairs Manager, Regulatory Strategy (Americas)

Bio-Rad Laboratories; Denver (CO); On-site; USD 138,000 - 189,000; Full time

Benefits offered by this job

Competitive medical plans

401k with profit sharing

Employee stock purchase program

Education benefits

Wellbeing programs

Job summary

Bio-Rad Laboratories’ Food Science Division is seeking a Scientific Affairs Officer to lead scientific strategies supporting regulatory submissions and product validations in the Americas. This role requires collaboration across functions to align science with business priorities.

The candidate will manage external validations, coordinate regulatory documents (AOAC, Health Canada), and engage with regulators and key stakeholders while ensuring policy compliance and rigorous scientific rigor.

Qualifications

• Advanced degree in a relevant scientific discipline.
• Minimum 5 years in scientific affairs or related field.
• Experience with regulatory submissions and validation processes.
• Strong written and verbal communication skills.

Responsibilities

• Oversee scientific strategies to support validations and US/AMER submissions.
• Coordinate and prepare scientific documents and regulatory responses.
• Collaborate with Marketing and cross-functional teams to align science with priorities.
• Supervise strategic scientific partnerships in the Americas.
• Stay updated on scientific advances and regulatory guidelines.
• Represent Bio-Rad with regulators and external stakeholders.
• Ensure regulatory compliance and internal policies.

Skills

Scientific writing

Regulatory submissions

Project management

Cross-functional collaboration

Analytical skills

Education

PhD or master's degree

Job description

Bio-Rad Laboratories’ Food Science Division is seeking a Scientific Affairs Officer to lead scientific strategies supporting regulatory submissions and product validations in the Americas. This role requires collaboration across functions to align science with business priorities.

The candidate will manage external validations, coordinate regulatory documents (AOAC, Health Canada), and engage with regulators and key stakeholders while ensuring policy compliance and rigorous scientific rigor.