Site Administrator at BMD & CO

BMD & CO; Athlone; On-site; EUR 32,000 - 42,000; Full time

Job summary

BMD & CO in Athlone, Ireland, is seeking a diligent Site Administrator to support the project team on a full-time, on-site basis.

The role focuses on accurate daily record-keeping, maintaining the site diary, recording craft time, and ensuring quality records are filed and submitted on time.

You'll handle document management, control critical documents via the project database, manage inductions and training records, and assist with general office duties on site.

Qualifications

• Leaving Certificate with higher level education desirable.
• Experience in Life Sciences Industry is beneficial.
• Knowledge of ISO9001:2015 helpful.

Responsibilities

• Oversee document management processes for the business.
• Maintain the site diary and track daily activities.
• Record craft time accurately for payroll and cost reporting.
• Liaise with visitors on site and support general office duties.
• Input site instructions on M-Site and archive files.

Skills

Attention to detail

Document management

Time management

Communication

Organisational skills

Education

Leaving Certificate (higher level desirable)

Life Sciences industry experience beneficial

ISO9001 knowledge beneficial

Tools

Microsoft Word

Microsoft Excel

Outlook

M-Site

Job description

Apply for Site Administrator at BMD & CO in Athlone, WH, IE.

This Full time on site position offers great opportunities for career growth.

We're looking for a diligent, detail-focused Site Administrator to support our project team, with a strong emphasis on accurate daily record-keeping. The core of this role is maintaining the site diary and recording craft time - accurate, detailed work that our cost and payroll processes depend on, so a genuine eye for detail and consistency is essential.

Alongside this, you'll support document management and control, quality records and Good Documentation Practices, ensuring critical project documents are filed, tracked, and submitted on time. This is a role that suits someone highly organised and methodical, who takes pride in getting the detail right and maintaining accuracy across repetitive, high-volume tasks.

A typical day looks like: Oversee and manage document management processes for the business. Filing of company quality records. Control of critical documents via the project database Submission and tracking of documentation. Calendar/diary management Good Documentation Practices. Responsible for induction planning of new starters. Responsible for processing all training records. Complete other administrative tasks to support the overall business which may arise.

General office duties including liaising with visitors on site, monitoring the site telephone document scanning and filing, Sending reports to client and sub-contractors, inputting site instructions on M-Site and archiving files.

Education, Training & Experience Leaving Certificate, with higher level education desirable. Experience in Life Sciences Industry. Knowledge of ISO9001:2015 beneficial. PC literate with competency in Microsoft Office Suite (Word/Excel) Outlook. Knowledge of document controls systems beneficial.

Competencies: Diligent, has a high level of attention to detail, and sets a high standard of quality for themselves and others. Strong Communicator, written and verbal. Strong numeracy skills. Personable, and a team player. Hard working and able to work in fast paced work environment. Ability to handle multitask and work well under pressure Accountable, someone who take ownership of tasks from beginning to end. Organised person who can self-prioritise work. Decisive, able to make decisions while lacking some information. Able to positively influence others to support shared goals.