HSE Supervisor – Biosimilar

About the role

The HSE Supervisor – Biosimilar will ensure a safe working environment across production areas, laboratories and utilities, aligning daily operations with Algerian HSE legislation, biosafety standards and GMP requirements.

Key responsibilities

• Ensure daily HSE presence in production areas, laboratories and utilities, guaranteeing compliance with HSE, biosafety and GMP rules.
• Oversee biological and chemical risk management, including containment, decontamination, and waste handling for biosimilar products and GMOs.
• Maintain regulatory compliance with Algerian HSE legislation, WHO guidelines, ISO 14001 and ISO 45001, and support internal and external audits.
• Lead training, incident investigation, CAPA implementation and HSE KPI reporting.

Required profile

• 6‑10 years or more of experience in HSE supervision within pharmaceutical or biotech manufacturing.
• In‑depth knowledge of Algerian HSE legislation, biosafety levels (BSL‑1 to BSL‑3) and GMP/GLP environments.
• Proven ability to work cross‑functionally with production, engineering, quality and maintenance teams.

Required skills

• Biological risk management and biosafety (BSL‑1, BSL‑2, BSL‑3).
• Chemical hazard management (REACH, CLP/GHS, SDS).
• Environmental and occupational health management systems (ISO 14001, ISO 45001).
• Safety tools such as LOTO, JSA, HAZOP, risk registers and CAPA.
• HSE KPI monitoring and dashboard reporting.
• NEBOSH, IOSH or equivalent HSE certification (strong asset).