HSE Lead for Pharma Manufacturing & Compliance

Amaris Consulting; Eigenbrakel; Hybride; EUR 70 000 - 100 000; Plein temps

Avantages offerts par ce poste

Health insurance

Remote work

Meal vouchers

Time savings account

Referral bonus

Résumé du poste

Amaris Consulting seeks an experienced HSE professional to join the Bio Drug Substance Manufacturing B7 team in Belgium. You will define priorities, manage permits, and drive compliance during shutdowns and ramp-ups, collaborating with production, engineering, and site teams to ensure a safe start-up and increased capacity.

The role requires 5–8 years in HSE, risk management, and strong project coordination, plus fluent French and a hands-on, solution‑oriented approach.

Qualifications

• Minimum 5 to 8 years of relevant HSE experience.
• Strong knowledge of environmental health and safety requirements in pharma/manufacturing.
• Experience managing incidents, CAPAs, audits, and risk assessments.
• Ability to lead HSE topics independently in a complex manufacturing environment.
• Fluent French with structured, hands-on, solution-oriented approach.

Responsabilités

• Define and coordinate HSE priorities, action plans, and prevention plans for the B7 organization.
• Coordinate work permits, fire permits, contractor activities, and co-activities during shutdown and ramp-up.
• Support incident, near-miss, deviation, CAPA, audit, and risk assessment activities, including investigation and follow-up.
• Maintain HSE compliance activities, workstation risk assessments, safety equipment inspections, and legal requirements.
• Organize HSE communications, training sessions, awareness initiatives, GEMBA walks, and participation in HAZOP activities.
• Lead project planning, task tracking, KPI monitoring, and stakeholder coordination for remediation, equipment implementation, and facility projects.

Connaissances

HSE management

EHS compliance

Risk management

Project coordination

Incident investigation

Stakeholder mgmt

French language

Description du poste

Amaris Consulting seeks an experienced HSE professional to join the Bio Drug Substance Manufacturing B7 team in Belgium. You will define priorities, manage permits, and drive compliance during shutdowns and ramp-ups, collaborating with production, engineering, and site teams to ensure a safe start-up and increased capacity.

The role requires 5–8 years in HSE, risk management, and strong project coordination, plus fluent French and a hands-on, solution‑oriented approach.