Risk Manager

Solvexis by Studibo; Region Sjælland; On-site; DKK 520,000 - 900,000; Full time

Job summary

Solvexis Consult is seeking an experienced Risk Coordinator to support a pharmaceutical CQV project, coordinating RAMS, risk assessments, and permit-to-work activities on-site. You will work closely with workstream leads and disciplinary teams to ensure safe planning and execution during turnover and commissioning.

The role emphasizes practical hazard identification, on-site guidance, and collaboration across electrical, mechanical and process safety disciplines to maintain a strong safety

Qualifications

• Bachelor's or Master's degree in Environmental, Health and Safety or related discipline.
• Strong background in EHS management.
• Pharmaceutical CQV/start-up project experience.
• Process Safety Management and risk reduction experience.
• Experience facilitating risk assessments and reviewing RAMS.
• Knowledge of Control of Work, Permit-to-Work, and LOTO.
• Familiarity with GMP environments and regulatory requirements.
• Experience with multidisciplinary construction, commissioning and turnover teams.
• Knowledge of EIDA or equivalent document management systems.
• Strong communication and coordination skills for on-site guidance.

Responsibilities

• Coordinating daily RAMS activities and following up on tasks.
• Facilitating risk assessments across multiple workstreams and CQV activities.
• Reviewing method statements, safe systems of work and RAMS.
• Supporting risk reduction during turnover and CQV with workstream leads.
• Participating in daily work coordination and planning meetings.
• Reviewing Permit-to-Work documentation and risk assessments.
• Collaborating with electrical, mechanical, LOTO and PTW coordinators for safe commissioning.
• Conducting site walks to support risk assessments and maintain EHS presence.
• Providing guidance on hazard identification and safe working practices.
• Promoting safety culture and continuous improvement.

Skills

RAMS facilitation

Risk management

Permit-to-Work

LOTO

EHS management

Hazard identification

Site coordination

Effective communication

Education

Bachelor's/Master's in EHS

Tools

EIDA

Job description

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.