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The OHS Specialist is responsible for driving and proactively lead efforts to create and maintain a safe working environment and safety culture. Contributes to OHS leadership and provides technical expertise to ensure ongoing regulatory compliance and continuously OHS improvements.
About the Team / The department
The EHS function is part of the global EHS organization and is responsible for all EHS tasks for site Copenhagen including the EHS management system (ISO 140001, ISO 450001 & ISO 50001). The EHS function is headed by senior EHS manager with reference to CPH site head.
Due to being a must to know Danish Legislation for the performance of this role, it is required that you possess full proficiency in Danish, both oral and written.
Your responsibilities:
- Leads site efforts to build a safe work culture. Partners closely with the senior EHS manager, site leadership and management staff to create a safe working environment and minimize operational risk.
- Mentors and supports the site safety organizations including OHS Committee and serves as OHS subject matter expert
- Responsible for coordinating the day to day occupational health and safety work at AGC Biologics A/S
- Advises the organisation on relevant issues concerning occupational health and safety and coordinates this, as well as being the contact person to the authorities.
- Evaluates regulatory requirements and establishes appropriate working environment programs and processes to ensure ongoing compliance.
- Analyzes and evaluates working environment performance to identify and implement opportunities for continuous improvement and facilitates OHS groups in the use of safety analysis tools and methods.
- Participates in maintaining and improving the ISO 45001 management system
- Technical OHS support in small and large engineering projects and changes to ensure compliance with OHS regulatory requirements and company policies and review safety work plans to ensure a safe design.
- Performs OHS risk assessments of new equipment, processes and projects to ensure compliance with regulatory requirements, reduce the potential for injury and minimize working environmental impacts
- Establishes an effective OHS reporting, incident investigation, root cause analysis and corrective action process. Able to lead/champion investigations involving serious incidents.
- Evaluates new client molecules for occupational health and safety risk.
- Provides oversight of the site emergency preparedness and planning process, procedures, and the formation and training of an emergency response team.
You should have:
- Comprehensive knowledge of health and safety laws and regulations including emergency planning
- Expertise within working environment aspects, behavior-based safety, industrial hygiene, and safety analysis methods (i.e. job safety incident analysis, risk assessment tools, WPA and control strategies)
- Knowledge and experience of ISO 45001
- Effective training techniques and skills
- Good communication skills and fluency in English
- Well-developed interpersonal, written communication, presentation and facilitation skills with ability to partner with all levels of the organization
- Ability to collect and analyze data, assess risk factors and identify solutions to complex problems
- Ability to work independently and in a team environment.
- Ability to work on a flexible work schedule including an on-call basis
- Computer proficiency in software applications required for analyzing, monitoring, reporting and presentations.
Your experience and educational background:
- Bachelor or Master's degree in Chemical, Process, or Technical Engineering or equivalent
- Minimum of 7 years’ experience in health and safety management
- Experience from process industry or biopharmaceuticals or chemical industries is preferred.
Join an international and agile organization
At AGC, you will get great opportunities to work with a wide array of tasks and challenges, and you will get experience with our various departments. Furthermore, as we plan projects and tasks together in the team, you will get the opportunity to influence your daily work. AGC offers an informal working environment where high energy and enthusiasm is part of the daily work life. We respect each other and our individual differences. At AGC, we have a flexible attitude and we help each other reach deadlines as a team.
Contact and application
For any further questions, your are more than welcome to contact the Hiring Manager for this role: Shahida Hamid at [email protected]. Please be aware that we take in consideration only the applications send via our career page and, not via email. We will process the applications as they arrive.
Want to keep posted about our growth and to learn more about our company?
We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !
AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.
Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 3.2.2022, men kan have været deaktiveret og genaktiveret igen.
- Øvrige
- København
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