Lead and manage the Environment, Health & Safety function across the pharmaceutical manufacturing site to ensure full compliance with local regulations, global standards, and company policies. Responsible for developing, implementing, and continuously improving EHS management systems to maintain a safe, healthy, and environmentally responsible workplace.

1. EHS Strategy & Compliance

• Develop and implement EHS policies, procedures, and programs aligned with pharmaceutical GMP requirements.
• Ensure full compliance with local environmental, occupational health, and safety regulations.
• Conduct regular compliance audits, risk assessments, and safety inspections across all departments.
• Lead preparation for external regulatory inspections related to EHS.

2. Safety Management

• Establish and supervise safety processes, including permit-to-work, equipment safety, hazardous substances, and waste management systems.
• Oversee accident/incident investigations, root cause analysis, and corrective action implementation.
• Ensure proper control of high-risk activities (confined space, working at heights, electrical work, etc.).

3. Environmental Management

• Monitor and control environmental aspects including emissions, energy consumption, wastewater, and waste disposal.
• Implement environmental sustainability initiatives in line with company and regulatory expectations.
• Maintain environmental records and reports for regulatory bodies.

4. Training & Development

• Develop EHS training programs for all employees and contractors.
• Conduct awareness sessions on emergency response, hazard identification, PPE usage, and safe practices.
• Build a strong safety culture across the site.

5. Emergency Preparedness

• Lead the site Emergency Response Plan and ensure readiness of fire systems, alarms, evacuation procedures, and emergency teams.
• Conduct emergency drills and revise procedures as needed.

6. Documentation & Reporting

• Maintain EHS documentation, logs, reports, and KPIs in compliance with GMP and internal standards.
• Prepare periodic reports for senior management on incidents, trends, and action plans.
• Oversee EHS internal audits and ensure CAPA completion.

7. Cross-functional Collaboration

• Act as the EHS focal point for production, quality, engineering, and maintenance teams.
• Support engineering projects with EHS assessments and approvals.
• Collaborate with HR, training, and operations to promote a culture of safety.

Qualifications:

• Bachelor’s degree in Science, Engineering, or related field (preferred: Chemical Engineering, Environmental Engineering, Industrial Safety).
• 9–12 years of experience in EHS within pharmaceutical Industry
• Strong knowledge of GMP, ISO 45001, ISO 14001, and regulatory EHS requirements.
• Experience in leading audits, investigations, and safety programs.
• Certified safety or environmental professional is a plus (NEBOSH, OSHA, IOSH).

Experience from 9-12 Years

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