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Product Safety Specialist - Job Opportunity at BD

Le Pont-de-Claix, France
Full-time
Mid-level
Posted: April 3, 2025
On-site
EUR 36,400 - 65,500 per year

Benefits

Competitive compensation package
Professional development opportunities
Global healthcare company exposure
Cross-functional project work

Key Responsibilities

Lead product safety strategy and compliance for medical device development
Represent medical affairs in cross-functional project teams
Develop and validate product safety testing protocols
Evaluate biocompatibility requirements for product changes
Coordinate with international stakeholders on safety standards
Author technical documentation and safety reports
Manage relationships with external testing partners

Requirements

Education

Master's degree in toxicology or biochemistry applied to health

Experience

2+ years in pharmaceutical product development

Required Skills

Knowledge of ISO 13485, design control, ISO 14971, ISO 10993, IEC 62366, and biocompatibility Scientific information review and synthesis English and French communication skills Computer proficiency Cross-cultural collaboration Project management

Certifications

ISO standards knowledge (10993, 13485, 14971) IEC 62366 familiarity
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Sauge AI Market Intelligence

Industry Trends

Increasing regulatory scrutiny in medical device safety is driving demand for specialized safety expertise Growing emphasis on biocompatibility in medical device development creates need for advanced toxicological knowledge Shift towards integrated safety assessment throughout product lifecycle requires broader skill sets Rising importance of international standards compliance due to global market access requirements

Salary Evaluation

The offered salary range aligns with market standards for medical device safety specialists in France, though top performers with advanced degrees can command higher compensation in major medical technology hubs

Role Significance

Typically part of a 5-10 person medical affairs team, collaborating with 20-30 cross-functional team members
Mid to senior-level position with significant influence on product development decisions and regulatory compliance strategy

Key Projects

New medical device safety validation programs Product modification safety assessments Regulatory documentation preparation Safety testing protocol development Cross-functional safety review processes

Success Factors

Deep understanding of international safety standards and regulations Strong project management capabilities in complex regulatory environments Excellent cross-cultural communication skills Ability to translate technical requirements into practical testing protocols Strategic thinking in risk assessment and mitigation

Market Demand

High demand driven by expanding medical device market and increasing regulatory requirements for safety documentation and testing

Important Skills

Critical Skills

Regulatory standards expertise is fundamental for ensuring compliant product development Cross-cultural communication enables effective global team collaboration Technical documentation skills ensure proper safety validation records

Beneficial Skills

Project management capabilities enhance cross-functional coordination Understanding of manufacturing processes aids in safety assessment Knowledge of emerging safety testing methodologies provides competitive advantage

Unique Aspects

Combination of technical expertise and cross-cultural collaboration requirements
Direct impact on patient safety through product development
Exposure to cutting-edge medical device technologies
International regulatory environment navigation

Career Growth

2-4 years in role before advancement, depending on project success and regulatory expertise development

Potential Next Roles

Senior Product Safety Manager Medical Affairs Director Regulatory Affairs Manager Quality Assurance Director Product Development Lead

Company Overview

BD

BD is a leading global medical technology company with significant market presence in medical supplies, devices, and laboratory systems

Fortune 500 company with strong international presence and reputation for innovation in healthcare technology
Strategic location in French medical technology hub with connections to European regulatory bodies
Matrix organization emphasizing cross-functional collaboration and international project teams
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