Conduct routine environmental inspections to ensure construction activities comply with environmental regulations, project requirements, and company procedures. •
Monitor environmental control measures, including dust, noise, waste management, water quality, erosion, sediment control, and housekeeping practices at project sites. •
Assist in implementing the Project Environmental Management Plan (EMP) and Environmental Management System (EMS) requirements. •
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Implement and maintain the Project Safety and Health Management System to ensure compliance with occupational safety and health legislation, company policies, and project requirements. •
Develop and review safety plans, risk assessments (HIRARC/JSA), method statements, and control measures to minimise workplace hazards. •
Conduct routine safety inspections, audits, and compliance assessments to identify hazards and ensure corrective actions are effectively implemented. •
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Bachelor's Degree or Diploma in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Life Sciences, or a related field.
Minimum 1-2 years of experience in pharmaceutical regulatory affairs or product registration. Fresh graduates with relevant internship experience are encourage to apply.
To ensure occupational safety and health activities, monitoring environmental control systems, and ensuring compliance with applicable EHS legislation, local requirements, and management system standards. The role focuses on plant safety, environmental performance, fire safety compliance, and continual improvement of EHS systems.
Prepare, compile, review and submit product registration and variation applications to the relevant regulatory authorities (e.g., NPRA).
Monitor the status of product registrations, renewals, amendments and variations. Ensure all product registrations are maintained in compliance with current regulatory requirements.
Liaise with regulatory authorities regarding product registration matters and respond to queries promptly. Coordinate with internal departments such as R&D, Quality Assurance, Production, Purchasing, Marketing and Sales to obtain required documentation.
...
Prepare, compile, review and submit product registration and variation applications to the relevant regulatory authorities (e.g., NPRA).
Monitor the status of product registrations, renewals, amendments and variations. Ensure all product registrations are maintained in compliance with current regulatory requirements.
Liaise with regulatory authorities regarding product registration matters and respond to queries promptly. Coordinate with internal departments such as R&D, Quality Assurance, Production, Purchasing, Marketing and Sales to obtain required documentation.
...
Prepare, compile, review and submit product registration and variation applications to the relevant regulatory authorities (e.g., NPRA).
Monitor the status of product registrations, renewals, amendments and variations. Ensure all product registrations are maintained in compliance with current regulatory requirements.
Liaise with regulatory authorities regarding product registration matters and respond to queries promptly. Coordinate with internal departments such as R&D, Quality Assurance, Production, Purchasing, Marketing and Sales to obtain required documentation.
...
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