Risk Coordinator - Pharmaceutical Project

Solvexis Consult; Hillerød; On-site; DKK 600,000 - 900,000; Full time

Benefits offered by this job

Structured onboarding

Administrative support

Documentation assistance

Regular follow-up

Job summary

Solvexis Consult is seeking an experienced Risk Coordinator to support a pharmaceutical project during turnover, commissioning, qualification and validation (CQV). You will coordinate RAMS, assess low/medium risks, and assist with high‑risk activities on site.

The role emphasizes structured risk management, collaboration with discipline leads, and ensuring safe commissioning and regulatory compliance throughout CQV.

Qualifications

• A bachelor’s or master’s degree in Environmental, Health and Safety, or a closely related discipline.
• Strong background in EHS management and pharmaceutical CQV projects.
• Experience facilitating RAMS and reviewing risk documentation.
• Familiarity with Permit-to-Work, LOTO and GMP regulatory expectations.

Responsibilities

• Coordinate daily RAMS activities and follow up on tasks.
• Facilitate risk assessments across multiple workstreams and high‑risk activities.
• Review method statements and safe systems of work.
• Support turnover and CQV risk reduction with workstream leads.
• Participate in daily planning meetings and on‑site coordination.
• Ensure QA of risk management and control documentation.

Skills

RAMS facilitation

EHS management

Risk assessment

CQV experience

Permit-to-Work

LOTO

Regulatory knowledge

GMP understanding

Cross-functional coordination

On-site governance

Education

Bachelor’s or Master’s in Environmental, Health and Safety

Tools

EIDA

Job description

Risk Coordinator - Pharmaceutical Project

Full time | Solvexis Consult | Denmark

Posted On 17-09-2026

Job Information

Job Opening Status In-progress

Construction

Work Experience 4-5 years

City Hillerød

State/Province Sjælland

030353

Job Description

Risk Coordinator – Pharmaceutical Project

Working hours: 40 hours per week

Start: As soon as possible

Assignment duration: Until 28 February 2027

About the position

Solvexis Consult is looking for an experienced Risk Coordinator to support a pharmaceutical project during turnover, commissioning, qualification and validation (CQV).

You will coordinate the daily preparation and review of risk assessments and method statements (RAMS), conduct assessments for low- and medium-risk activities, and support the assessment of high-risk work.

The role combines structured risk management with an active presence on site. Working closely with workstream leads, technical disciplines and Permit-to-Work and LOTO Coordinators, you will help ensure that activities are properly assessed, planned and executed safely.

Responsibilities

Your primary responsibilities will include:

• Coordinating daily RAMS activities and following up on outstanding tasks.
  
• Facilitating risk assessments across multiple workstreams, including conducting low- and medium-risk assessments and supporting high-risk activities.
  
• Reviewing method statements, safe systems of work and task-specific risk assessments.
  
• Supporting workstream leads in identifying, evaluating and reducing operational, process safety and EHS risks during turnover and CQV.
  
• Participating in daily work coordination and planning meetings.
  
• Supporting the review of Permit-to-Work documentation and associated risk assessments.
  
• Working closely with electrical, mechanical, LOTO and Permit-to-Work Coordinators to support safe commissioning and qualification activities.
  
• Conducting site walks to support risk assessments and maintain a visible EHS presence.
  
• Providing practical guidance on hazard identification, safe working practices and compliance with project and regulatory requirements.
  
• Checking the quality and completeness of risk management and Control of Work documentation.
  
• Promoting a strong safety culture and contributing to continuous improvement.
  

Qualifications and experience

We expect that you have:

• A bachelor’s or master’s degree in Environmental, Health and Safety, or a closely related discipline.
  
• A strong background in EHS management.
  
• Experience from pharmaceutical projects during CQV and/or start-up.
  
• Experience in Process Safety Management, including hazard identification and risk reduction.
  
• Practical experience facilitating risk assessments and reviewing RAMS.
  
• A sound understanding of Control of Work, Permit-to-Work systems and LOTO.
  
• Familiarity with pharmaceutical regulatory requirements, EHS expectations and GMP environments.
  
• Experience supporting multidisciplinary construction, commissioning and turnover teams.
  
• Knowledge of digital project information platforms such as EIDA or equivalent engineering and document management systems.
  
• Strong communication and coordination skills, with the ability to translate risk requirements into practical site guidance.
  

What we offer

At Solvexis, you will be supported throughout your assignment through structured onboarding, administrative support, documentation assistance and regular follow-up.

You will join a pharmaceutical project where your contribution directly supports safe working practices and coordination across technical disciplines.

Employment terms will be agreed based on your qualifications, experience and the conditions of the assignment.