At Excelya, we embody Audacity, Care, and Energy in all that we do. We offer a dynamic and inclusive environment where innovation and collaboration drive success.

The Pharmacovigilance Associate ensures drug safety compliance by managing safety reports, supporting risk management activities, and communicating with stakeholders. The role requires a life sciences background, pharmacovigilance experience, and strong organizational, communication, and teamwork skills.

Main responsibilities:

• Ensure compliance with pharmacovigilance regulations, company procedures, and quality standards.
• Manage Individual Case Safety Reports (ICSRs) in accordance with local legislation and internal guidelines.
• Communicate relevant safety information to health authorities, stakeholders, and external partners.
• Support safety surveillance activities, including risk management, safety issues, and product-related alerts.
• Contribute to the creation and maintenance of quality documents and ensure proper documentation practices.
• Deliver training on pharmacovigilance processes to internal employees.
• Collaborate with third parties involved in pharmacovigilance activities.
• Promote adherence to corporate policies, values, and compliance standards, including HSE requirements.

Requirements

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities:

• Support the operational management of ongoing clinical studies.
• Contribute to study oversight and coordination activities.
• Collaborate with internal and external stakeholders, including CRO partners and study teams.
• Ensure compliance with applicable regulations, GCP and study procedures.
• Assist with workload management and operational delivery during a peak activity period.

Requirements

Own Your Internship Adventure at DOF

We would like to invite enthusiastic, curious, forward-thinking engineering students from NTU Singapore to join us on a 20-week Credit Bearing internship program. The Intern Engineer is one of the best ways to gain deep understanding and insights into the offshore industry and operations.

Responsibilities

·       Learn about offshore industry standards and their practical applications

·       Join Project Management Teams and contribute to fruition of ongoing projects

·       Development of technical deliverables that will be utilized in both live operations and tendering applications

·       Possible secondment to relevant teams, such as Structure, Naval and/or Drafting

Requirements

·       3rd or 4th Year student from B.Eng Civil or Mechanical Engineering currently studying at NTU Singapore

·       Proficient in Microsoft Word, Excel and Powerpoint

·       Excellent communication with strong analytical skills

·       Enjoy working in collaborative environment where we share success / focus on teamwork

·       Identify with DOF core values of Respect, Integrity, Teamwork, Excellence and above all, we are SAFE

Location: Singapore

Commencement: Semester 2 Internship : January 2027 - May 2027

Antipollution, a member of

V Group (Vasileiadis Group), is a leading provider of environmental and

integrated waste management solutions in the Eastern Mediterranean, Egypt,

and the Balkans. Through our commitment to sustainability, innovation, and

operational excellence, we deliver specialized environmental services across

a wide range of industrial and infrastructure projects.

As part of our continuous

growth, we are seeking a highly motivated Site Supervisor to join our team,

based at our Headquarters in Piraeus.

Role Overview

The successful candidate

will be responsible for supporting and supervising asbestos removal projects

throughout all implementation phases, including site inspections, project

costing, work planning, and on-site supervision, ensuring full compliance

with health, safety, and environmental requirements.

Requirements

Key Responsibilities

1. Site Inspections & Project Assessment

Join Excelya, a dynamic and innovative company committed to excellence and collaboration in the field of translational research.

As a Research Assistant in Histopathology, you will contribute to the preparation, processing, and analysis of biological tissue samples to support research projects across various therapeutic areas.

Key responsibilities include:

With several long-term projects secured, DOF continues to grow and we are now looking for a Project Procurement Lead to join our Subsea project organisation.

Responsibilities:  

As Project Procurement Lead, you will be responsible for planning and managing procurement activities for assigned subsea projects, from tender support and project start-up through execution and close-out. You will work closely with Project Managers, Engineering, Commercial, Finance, Legal, Operations and Supply Chain teams to ensure procurement is aligned with project scope, schedule, budget, risk and client requirements.

This is primarily a project procurement management role. You will develop procurement plans, manage procurement forecasts, lead sourcing and subcontracting activities, follow up suppliers and subcontractors, and ensure procurement risks are identified, communicated and managed.

Join the Skandi Mercury team as Master (Internal applicants only)

Application Deadline 17.06.2026

DOF is pleased to announce an internal opportunity on board Skandi Mercury as we continue to deliver safe and efficient offshore operations for one charter.

We are looking for a Master to join the vessel from 21.07.2026
A 2-3 week handover period prior to embarking may be expected.

Rotation: 4 weeks
Operational area: Brazil

As part of the crew on Skandi Mercury, you will play an important role in day‑to‑day operations, contributing to safe execution of work and maintaining DOF’s high operational standards.

We value our employees and aim to provide an environment that supports teamwork, development, and professional growth. This role offers an opportunity for internal candidates who wish to further develop their career within DOF.

Who we are 

DOF is a leading provider of integrated marine and subsea services to the global offshore energy market. We combine expertise, assets, and technology to execute integrated subsea and offshore operations safely, and reliably - every time. 

At Excelya, we are committed to fostering an environment defined by Audacity, Care, and Energy. As a Clinical Operations Lead , you will play a vital role in enhancing our clinical research strategies and ensuring operational excellence across our studies.

This position offers a unique opportunity to lead strategic CMC regulatory initiatives while collaborating with cross-functional stakeholders to ensure the highest standards of quality and compliance. You will play a key role in driving regulatory excellence, supporting complex global submissions, and contributing to innovative development and lifecycle management strategies that shape the future of medicines.

Main responsibilities :

Join Excelya, a company driven by Audacity, Care, and Energy, where innovation and collaboration are at the heart of everything we do. As a Clinical Scientist, you will be a key player in supporting clinical trials and contributing to the advancement of clinical research projects.

You will work alongside cross-functional teams to ensure clinical studies are conducted in accordance with protocol, regulatory requirements, and company standards. Your role will involve reviewing clinical data, supporting medical monitoring activities, and contributing to the development and review of clinical trial documents.

• Support clinical trial activities from study start-up to close-out, ensuring adherence to clinical and regulatory standards.
• Contribute to the preparation and review of protocols, informed consent forms, and amendments.
• Perform medical review of clinical data, including patient profiles and adverse event narratives.
• Collaborate with pharmacovigilance, clinical operations, and biostatistics teams for data review and interpretation.
• Assist in medical writing and review of study-related documents such as clinical study reports and briefing documents.
• Ensure proper documentation and filing of study-related materials into Trial Master Files.
• Support preparation for audits, inspections, and regulatory submissions.

Requirements

About You

Join the Skandi Vega team as AB

Application Deadline 28.06.2026

DOF is pleased to announce an internal opportunity on board Skandi Vega, as we continue to deliver safe and efficient offshore operations.

We are looking for a AB to join the vessel from 22.07.2026. AHTS experience preferred.
A handover period prior to embarking may be expected.

Rotation: 4 weeks
Operational area: North Sea

As part of the crew on Skandi Vega, you will play an important role in day‑to‑day operations, contributing to safe execution of work and maintaining DOF’s high operational standards.

We value our employees and aim to provide an environment that supports teamwork, development, and professional growth. This role offers an opportunity for internal candidates who wish to further develop their career within DOF.

Who we are 

DOF is a leading provider of integrated marine and subsea services to the global offshore energy market. We combine expertise, assets, and technology to execute integrated subsea and offshore operations safely, and reliably - every time.