Manager EHS Compliance & Site Security EMEA at Clairo

Hanover, Lower-Saxony, Germany

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Automotive, ManufacturingIndustries

Requirements

Master’s degree in a relevant engineering discipline or equivalent qualification
Extensive experience with the European regulatory landscape, particularly in the industrial and manufacturing context
Several years of professional experience in an industrial environment
Proven management capabilities with strong management and organizational skills
Solid project management experience
Excellent communication and interpersonal skills, with the ability to engage effectively across all levels of the organization
Fluent in English and German

Responsibilities

Monitoring EHS regulations, assessing their impact, developing plans to implement changes, and follow-up on the progress
Reviewing and reporting on EHS compliance across all Clarios EMEA sites to ensure consistent standards and performance
Training affected stakeholders and building awareness around regulatory changes and resulting opportunities
Supporting the integration of regulatory changes into Clarios Management System procedures and instructions
Driving innovation in sustainability and compliance practices
Conducting site security reviews and implementing risk-based improvements
Evaluating and deploying new technologies aligned with business needs
Tracking security KPIs and incidents to optimize systems and reduce risks
Collaborating with insurance partners to ensure and maintain HPR fire protection status

Skills

EHS Compliance

Regulatory Monitoring

Risk Management

Site Security

Fire Protection

Audits

Stakeholder Training

Compliance Reporting

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters

1972Year Founded

$29.9MTotal Funding

GROWTH_EQUITY_VCCompany Stage

Biotechnology, HealthcareIndustries

5,001-10,000Employees

Benefits

Competitive and equitable total rewards package

Physical, mental and financial health and wellness

Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.

The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.

AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.

The company has nearly 50 years of experience in clinical trial technology solutions.

Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.

The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.

Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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