EHS Coordinator
- Denmark
- Contract
- Compliance / Quality Assurance
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for an EHS Coordinator to join them on their new expansion project. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
As an EHS Coordinator, you will be responsible for the delivery of activities on a complex drug manufacturing extension project.
Responsibilities:
- Be a part of the client's team and represent client in all matters overseeing and liaising with the Engineering Providers/General Contractors
- Review and challenge tender packages with respect to EHS (Environmental, Health & Safety) to ensure designer’s obligations are fulfilled
- Fulfill the roll of the statutory Health and safety coordination in design and provide the final journal of EHS matters
- Support and ensure that design reviews have clear and appropriate Health & Safety focus across disciplines and across project phases to ensure site standards and regulatory compliance to be followed through Detailed Design (ergonomics, accessibility, process hazards, etc)
- Review specifications with respect to EHS matters & regulations in collaboration with the designated CE role
- Participate in EHS related (i.e. with regards to 3D model space management, permitting, mock-up’s) meetings with Engineering Provider/General Contractor and suppliers
- Support Engineering Provider and team to get adequate involvement of end-users
- Support and assist the project EHS Team in overseeing and auditing the General Contractor’s Construction Management team (CM) with respect to the onsite safety procedures and compliance
- 8+ years of EHS experience.
- Ideally have experience with AMK-P or AMK - B
- EHS experience through the delivery of a large scale project.
- Must have knowledge and experience in the use of Denmark WEA (Working Environment Agency) regulations and interpretations.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
To view Quanta's privacy policy, please visit our website
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
Save as job alert
Similar Jobs
Salary
Competitive
Location
Clonmel
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
East
Description
QA Specialist- Life Science – Contract- Clonmel Our Partner in Tipperary area develops and supplies the active ingredients and final formulated product for a range of innovative medicines at its
Reference
31714
Expiry Date
01/01/0001
Author
Tom EvansAuthor
Tom EvansSalary
Competitive
Location
Dublin
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
Dublin
Description
Laboratory Technician - Pharmaceuticals - 12-Month Contract - Dublin Do you want to be involved with exciting Pharmaceutical projects? When it comes to the development and production of
Reference
32113
Expiry Date
01/01/0001
Author
Dawn HosierAuthor
Dawn HosierSalary
Competitive
Location
Arizona
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
Central
Description
Quality Director – Pharmaceuticals - Arizona We have an exciting opportunity for a Quality Director to join a Global biotech company located in Arizona for an initial 24-month contract. An
Reference
31670
Expiry Date
01/01/0001
Author
Annabel NangleAuthor
Annabel NangleInsights
Send us your CV
Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.
Megan
I manage this role.