EHS Manager-Pharma Sligo

at  Dillon Engineering Services

OVERVIEW

Dillon Engineering Services are seeking an experienced EHS Manager to join our client, a global biopharmaceutical company in Sligo. Reporting to the Site Director, you will be responsible for the overall direction of the EHS group onsite and managing site safety and environmental activities in line with relevant corporate and regulatory requirements.
This is an exciting opportunity join a dynamic and progressive company where you will lead and deliver programs, policies, and procedures to ensure that the site complies with all EHS requirements.

QUALIFICATIONS

• BSc in Occupational Safety & Health Level 8, or equivalent, or a degree in a related discipline is essential.
• MSc in Environmental Health and Safety Management (Level 9) is desirable.
• 3 - 5 years in an EHS role with detailed knowledge of cGMP and regulatory requirements relating to the pharma/med device industry.
• 5+ years of demonstrated project management experience, including the ability to deliver projects on schedule, within budget, and to predefined quality requirements.
• Minimum 2 years people management experience.
  Our client is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.

• The role emphasizes detailed knowledge of current Good Manufacturing Practices (cGMP), which are critical in biopharmaceutical operations to ensure product quality and safety.
• It involves compliance with stringent regulatory standards that govern the pharmaceutical industry, highlighting expertise in navigating complex legal and environmental requirements.
• Active participation in the introduction of new products or technical/product transfers reflects the dynamic nature of biopharmaceutical operations.
• The role applies EHS expertise to process design and redesign, ensuring adherence to pharmaceutical safety and environmental standards.
• afety risk assessments for processes and occupational activities, as well as environmental risk evaluations, are integral for meeting pharmaceutical production standards.
• Focus on process safety and occupational hygiene aligns with the biopharma industry’s high-stakes operational environment.
• Managing and maintaining permits related to environmental and health safety is essential for pharmaceutical sites, given the strict oversight by regulatory bodies.
• Development of Emergency Response and Occupational Health Services specifically tailored for biopharmaceutical contexts.
• Emphasis on EHS programs that align with operational needs of capital expenditure and large-scale site projects, ensuring they meet pharmaceutical compliance and operational standards.
• Harmonizing site EHS operations with broader corporate and pharmaceutical industry standards (e.g., ISO 14001, ISO 45001) ensures alignment with global quality and safety expectations.