Clause 7.1 of ISO 14001:2015 requires organization to determine and provide the resources needed for the establishment, implementation, maintenance and continual improvement of the environmental management system (EMS). There is no requirement to document this clause but rather to determine what resources are necessary for the implementation, maintenance and improvement of the EMS. Resource include people, equipment, finance, infrastructure, etc.
The best way to determine resources for the implementation is to develop project plan for the implementation and define what is necessary in the project plan. In case of maintenance of the EMS, resources are determined according to annual plan of activities within EMS, this includes environmental objectives and plans for achieving them, application of operational controls, internal audit, etc.
Old version of ISO 9001 required following six mandatory procedures:
- Control of documents (4.2.3)
- Control of records (4.2.4)
- Internal audit (8.2.2)
- Control of nonconforming product (8.3)
- Corrective action (8.5.2)
- Preventive action (8.5.3)
ISO 14001 doesn't have such specific requirements for the construction sites or any other type of business. But, if such activity is defined by the organization as an operational control for handling waste, it is compulsory to follow this control, otherwise it would be considered as nonconformity.
There is no requirement in the standard for internal auditors to be trained by exemplar certified organization. The only requirement in this regard is for organization to retain documented information about the trainer competency, but it refers to the trainer alone, not to the organization to which the trainer belongs.
How long do you have to repeal a Minor Finding with your registrar?
I assume you are asking, how much time does the organization have to remove minor nonconformity found during the certification audit. Usually the deadline for removing nonconformities is agreed with the certification body, and it depends on the scale of the nonconformity. In case of minor nonconformities, the deadline is usually one week, but there is no rule that defines the time frame explicitly.
Documentation required for Internal External and Interested parties
Answer: The new clauses introduced in the main part of ISO 27001:2013 do not require any specific documentation to be kept related to Internal, External and Interested parties.
Regarding Annex A, control A.18.1.1 - Identification of applicable legislation and contractual requirements, previously control A.15.1.1 on ISO 27001:2005), requires the documentation of Internal, External and Interested parties requirements, such as statutory, regulatory, contractual requirements, but you only have to do that if this control is considered applicable in your Statement of Applicability.
Answer: Considering ISO standards, I'd suggest you the ISO 22301 Lead Auditor and ISO 22301 Lead Implementer certifications. Other certifications you should consider are DRI Certified Business Continuity Professional (CBCP) and Certificate of the Business Continuity Institute (CBCI) from BCI.
Remote monitoring of Kronos Cloud and hosted environmnets
Remote monitoring of Microsoft Windows 2003/2008/2012 and Linux servers, which includes of Performance, uptime, SQL DB, website status, web based application & server resources
Responding to Alerts on monitoring tools
Identify the root cause and troubleshoot the server performance issues.
Handle Level1 Escalations, and adhere to escalation matrix
Good Administration skills over Windows and Linux OS.
Ensure operating standards are developed, maintained, and adhered to.
Can you please suggest is lead implementer certification will benefit me as I have interested in this course.
Answer: Yes. Besides helping you to understand and implement an ISO 27001 ISMS, a lead implementer course can help you understand how to apply controls in Annex A, which will help you evaluate and improve the activities you perform according your job description (e.g., controls from section A.12.4, related to logging and monito ring, and controls from section A.16, about Information security incident management)
DHF is abbreviation for Design History File which is a formal document that is prepared for each medical device. The DHF can be either a collection of the actual documents generated in the product development (PD) process or an index of documents and their storage location.
When it comes to risks and opportunities, the standard doesn't require full scale risk management that includes documented procedure, criteria for evaluation, etc. It only requires organization to determine risks and opportunities and take actions to address them. This can be done by arranging brainstorming session with relevant peo ple in the company and talking about risks and opportunities or using some tools like SWOT or PEST analysis. For more information, see: How to address risks and opportunities in ISO 9001 https://advisera.com/9001academy/blog/2016/06/21/how-to-address-risks-and-opportunities-in-iso-9001/