No deviation

EHS Associate

No deviation  •  Singapore, SG (Onsite)  •  3 hours ago
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Job Description

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

The EHS Associate / Coordinator supports day-to-day Environment, Health & Safety (EHS) operations within a regulated manufacturing environment, ensuring compliance with internal standards and Singapore Workplace Safety and Health (WSH) requirements. This role partners closely with operations, engineering, laboratory, facilities, and project teams to coordinate EHS programs, maintain documentation and compliance readiness, deliver training, support audits and incident management, and promote a strong safety culture. The successful candidate will also contribute to brownfield expansion projects, contractor safety, and continuous improvement initiatives while ensuring EHS actions are effectively tracked and completed

Key Responsibilities

  • Coordinate day-to-day EHS programs, meetings, action tracking, stakeholder follow-ups, reporting, and continuous improvement initiatives.
  • Support site safety campaigns, Serious Injury and Fatality Prevention (SIF) initiatives, safety stand-downs, and EHS performance monitoring.
  • Maintain EHS records, compliance documentation, training records, permits, and data within systems such as Cority, Humantech, INCA, GETS, SharePoint, and Smartsheet.
  • Prepare audit evidence and support regulatory inspections, internal audits, compliance reviews, and management reporting.
  • Deliver EHS training, toolbox talks, safety briefings, and awareness programs while tracking training completion and refresher requirements.
  • Coordinate workplace inspections, audits, incident investigations, risk assessments, CAPA activities, and corrective action follow-up.
  • Support industrial hygiene activities, ergonomics assessments, chemical management, LOTO program reviews, and contractor safety compliance.
  • Conduct workplace walkdowns to identify safety risks, unsafe behaviours, housekeeping issues, and opportunities for improvement.
  • Provide EHS support for laboratory, manufacturing, engineering, facilities, maintenance, and capital project activities.
  • Assist with change management, permit-to-work compliance, pre-start-up safety reviews (PSSR), design safety reviews, commissioning activities, and brownfield expansion projects.

Required Qualifications

  • Diploma or Degree in Environment, Health & Safety (EHS), Engineering, Science, Industrial Hygiene, or a related discipline.
    2–4 years of relevant experience in EHS, safety coordination, or operational support.
  • Experience within regulated manufacturing environments such as pharmaceuticals, semiconductors, laboratories, engineering, facilities, or related industries is preferred.
  • Registered Workplace Safety and Health Officer (WSHO) certification is an advantage.
  • Working knowledge of EHS management systems, risk assessments, audits, CAPA, permit-to-work systems, contractor management, and Singapore WSH regulations.
  • Strong communication, coordination, documentation, stakeholder management, and problem-solving skills.
  • Detail-oriented, proactive, able to work independently, and comfortable engaging with employees, contractors, and cross-functional teams.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.

No deviation

About No deviation

Founded in 2007, No deviation is a trusted partner to pharmaceutical and biotech companies seeking smarter ways to deliver compliance. From engineering consultancy to CQV execution, regulatory compliance, and digital enablement, we support our clients across the entire project lifecycle in Asia, Europe.

We specialise in:

CQV (Commissioning, Qualification & Validation)

Lean, risk-based approaches aligned with GAMP 5, Annex 15, and ASTM E2500.

Quality, Compliance & Regulatory

Audit readiness, QMS remediation, documentation, and training.

Project Management & Technical Support

From operational readiness to vendor coordination.

Digital Enablement

Implementation of paperless validation (e.g. Kneat Gx), data integrity, and process digitalisation.

Specialised Training & Talent Support

Upskilling programs and resource placement to accelerate project success.

Our approach is rooted in patient safety, process understanding, regulatory compliance, and a constant drive for operational excellence in terms of safety, quality, delivery, and cost.

If you’re troubleshooting a deviation, planning a major CQV deployment, or scaling digital validation tools, we work side-by-side with your teams to deliver meaningful outcomes. Our methodology draws from ICHQ9 risk principles, with a hands-on framework: Understand - Observe - Define - Implement.

Want to learn more about paperless CQV, digital QMS, or project-ready resources? We’re happy to talk. Visit nodeviation.com to explore how we can support you.

Industry
Chemicals & Materials
Company Size
51-200 employees
Headquarters
Singapore, SG
Year Founded
2007
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