Professional Documents
Culture Documents
For the benefits of internal auditors the list of questions to be asked to the respective department is
listed below based on ISO 9001-2015 and ISO 14001-2015 for EQHSMS system. Please note that it is
not exhaustive and it may be considered as guidelines only. Auditors are advised to prepare their own
question list based on the questions listed below.
1. EQHSMS system coordinator and ISO 9001 AND ISO 14001-2015 AND OHSAS 18001
system related areas
How do you arrive at quality and environmental and occupational, health and
1.
safety policy?
Have you identified objectives based on your Quality and environmental and
2.
occupational, health and safety policy?
Is your Quality and environmental and occupational, health and safety policy
3. complies with the requirements of ISO 9001 AND ISO 14001 EMS and OHSAS
18001 standards?
4. How do you ensure prevention of pollution through out the organization?
Have you considered the context of the organization’s overall business activities
? Have you determine external and internal issues in the Environment
management system (EMS)? Does this issues are relevant to its purpose and
5. ability to achieve intended outcome of EQHSMS? Have you considered the
context of the organization’s overall business activities and issues and quality and
environmental and occupational, health and safety conditions affected by your
activities? To whom you have identified your interested parties?
Have you determine the boundaries and applicability of the Environment
6.
management system?
Have you considered the context of the organization’s overall business activities
7. and issues and quality and environmental and occupational, health and safety
conditions affected by your activities?
8. To whom you have identified your interested parties?
Have you conducted environmental aspect and OHS Hazard analysis survey for
your all activities? Are all activities covered? How do you ensure that all activities
9.
are covered? To whom you have included in aspect and OHS Hazard analysis
survey?
What is your mechanism for evaluation of Impacts and Risk associated of each
10.
aspect and OHS Hazards?
Have you identified list of significant aspect and OHS Hazards? Have you done
11.
feasibility analysis for such significant aspect and OHS Hazards?
Have you prepared Environmental aspect and OHS Hazard Register? Is this
12.
register is made available to all employees?
Have you communicated all such Environmental aspect, OHS Hazards, its impact
13.
to all your employees within the organization?
What are the needs and expectations of interested parties in management
14. system? What procedure or process is followed to understand interested parties
requirements?
How do you establish the EQHSMS? How do you bring continual improvement in
15.
Environment management system in accordance of this international standard?
Have you conducted quality and environmental aspect analysis survey for your all
activities? Are all activities and products given in the scope are covered? How do
16.
you ensure that all activities are covered? To whom you have included in aspect
analysis survey?
What is your mechanism for evaluation of impacts of each aspect? Are you
17. having documented information for aspect-impact analysis and risk and
opportunities?
Have you identified list of significant aspect? Have you done feasibility analysis
18.
for such significant aspects?
Have you prepared Environmental Aspect Register? Is this register is made
19.
available to all employees related to their work areas?
Have you communicated significant Environmental aspects, its impact to all your
20.
employees within the organization?
21. Have you prepared documented information of legal and other obligations?
Are you complying all such requirements of compliance obligations? Have you
22. identified non-conformity related to compliance obligations? Is there any action
plan to comply such requirements?
23. Have you have reviewed the applicability of different rules and regulation?
24. Are you having list of applicable and not applicable rules and Acts?
How do you ensure that particular rules are not applicable? Are you having any
25.
justification for the same?
26. Who is looking for the day-to-day compliance of all such legal requirements?
How do you ensure that all objectives are inline with the requirements of your
Quality and environmental and occupational, health and safety policy? Does
27.
environment policy includes the framework for setting up the EQHSMS
objectives? Where do you documented EQHSMS objectives?
Is there any need to take special care for significant environmental aspects ? In
which case the significant environmental aspects are resulted in risk and
28.
opportunities? Can you show us such details and what action is taken for the
same?
What is the mechanism of identification of Environmental Health And Safety
29. Management Programmes? What are the EHSMP at present, frequency of review
and identification of new EHSMPs?
Have you determined the risks and opportunities related to EQHSMS issues,
30. environmental aspects and compliance obligations? Have you considered
potential environment situation?
Have you considered significant environmental aspects, compliance obligations
31.
and risk and opportunities in framing this objective?
Show us documented information of risks and opportunities, environmental
32. aspects, criteria defined for significance, list of significant aspects and action
taken.
Is there any documented information for your Quality and environmental and
occupational, health and safety policy Statement, objectives and person
33. responsible for it? How do you communicate environment policy and objectives
within the organization? Interview few people to ensure it is understood and
applied.
How and when do you review such objectives for achieving the targets? Have you
34.
prepared any plan for the same?
35. Are your objectives committing prevention of pollution?
What is the mechanism of identification of risk and opportunities? What is the
36. Quality and environmental and occupational, health and safety plan at present,
frequency of review and identification of new plans?
Who does routine monitoring and implementation of Quality and environmental
37. and occupational, health and safety plans? How the records of such Quality and
environmental and occupational, health and safety plans are maintained?
38. Are you having defined organization structure and responsibility?
39. How do you report to top Management for effective implementation of System?
40. How do you ensure continual improvement in the system?
Do you report to Top Management for effectiveness of Quality and environmental
and occupational, health and safety Management System? How do you measure
effectiveness of system for working of your Organization? How do you collect
41. necessary information for the same? Are you getting information for corrective
action taken on the identified non–compliances and it’s effectiveness for
discussion in the management review meeting? What is the frequency of the
Management Review Meeting?
How do you plan for management review meeting and who are committee
member? Do you circulate agenda for Management review meeting in advance?
Do you prepare minutes of Management review meeting with the actions decided
42.
in management review meeting? How do you monitor effectiveness of the
system? Are you reviewing quality and environmental and occupational, health
and safety objectives in the management review? When do you review it?
Are you doing follow-up for completion of action decided in Management review
43.
meetings? How? What is input and output of Management review meetings?
Does the master list for Documented information and Formats with revision no.
Made and communicated to concern person? Show us latest revision of Quality
and environmental and occupational, health and safety Manual? How do you
maintain master list of page-wise amendment? How do you inform all the persons
44. for changes in any documented information? Who is responsible for approval and
control of different types of documented information? Are you changing whole
document or page-wise amendment? How do you get information for changes in
the documented information / Quality and environmental and occupational, health
and safety Manual? How do you inform to the entire concerned person?
45. How documented information is identified for control / uncontrolled and obsolete?
46. Do you preserve obsolete documented information? Where do you preserve it?
47. Do you have list of trained auditors? Who has given training to them as per ISO
How do you improve the suitability, adequacy, and effectiveness of the QMS to
68. enhance performance? Have you determined is there needs or opportunities that
are addressed as a part of continual improvement?
Are you doing follow-up for completion of action decided in Management review
meetings? How? What is input and output of Management review meetings?
Have you analyzed data for:
a). Customer satisfaction.
69. b). Product conformities like inspection for incoming, in process and final
stage inspection.
c). Process trends and opportunities for the improvement for example yield
control, time cycle reduction etc.
d). Suppliers.
When do you carry out corrective actions? How do you identify causes of
70. nonconformity? Have you documented results of actions taken? Where? How do
you review the effectiveness of the action taken?
71. Have you fixed any action plan for the achievement of Quantifiable criteria? By
which data and how it will be achieved? Show us action plan for achieving the
20. Is all the above testing is being done through competent person?
Have you determine how these compliance obligations apply to your area? Is
there any system followed to include environmental and occupational, health and
21.
safety compliance obligations for establishing, implementing, maintaining and
continually improving the EQHSMS?
Who is responsible to ensure that the legal and other requirements are taken into
22. account in establishing, implementing and maintaining quality and environmental
and occupational, health and safety management system?
Does the organization respond to relevant communication on its quality and
environmental and occupational, health and safety management system? Is there
23.
any documented information of this communication? Do you ensure such
communication enables persons to contribute for continual improvement? How
Have you externally communicate information relevant to EQHSMS? Show us
24. what kind of communication is done by you externally? Does it cover all
information required by all applicable compliance obligations?
Have you established the process to evaluate fulfilment of organizations
compliance obligations? At what frequency you evaluate the compliance of
25.
organization? Do you have competent person for monitoring and understanding
of compliance status?
How do you retain documented information of compliance evaluation results?
Show us evidences that you fulfil such requirements against your obligations.
26.
What is evaluated for your compliance obligations? What records are maintained
for evaluation of compliance?
Are you having list of fire extinguishers, HOSE reel, fix hydrant system etc.? Are
27.
they covered under Preventive Maintenance?
Have you prepared Major Emergency Preparedness plan? Does it covers fire and
accidents? Is the training related to MEP is given to all employees? Have you
28.
conducted mock drill? What are the findings of mock drill? Show me records of
Mock drill?
Have you prepared Major Emergency Preparedness plan? Is the training related
29. to MEP is given to all employees? Is all the above testing is being done through
competent person?
3. Training and HR
Are you having list of employees? Have you identified personnel doing specific
1.
work affects environment?
Are such employees are competent to do the same? Are you having documented
2.
information of employee’s competence?
Have you determine competence of personnel performing work affecting
3. conformity to the product requirements? How? Based on that how do you identify
training needs or recruitment of new person for the various levels of employees?
What are the parameters covered under competence? Are you having
4. competence chart for the various levels of employees? How do you ensure the
competence and are you having annual appraisal to ensure competence of
Can you show us documented information for annual training as well as routine
24.
training? How do you prepare training calendar? Can you show us the same?
Do you implement action from risks and opportunities? Have you update risks
25.
based on such investigation in documented information?
Have you identified any training need for special activity based on multi skill
26.
analysis?
Do you get timely resources or delay to get resources? What are the steps at the
27.
time of un availability of resources?
4. Operation / Production
Are you having aspect / impact register of your all-applicable activities? Show me
1.
aspect impact register?
Is all aspect and its impacts are communicated to all your employees within the
2.
department?
Are you having list of significant aspects of your department? How the impact
3.
evaluation is done for all such aspects?
4. Have you plan, implemented processes as per ISO 9001 AND ISO 14001:2015
QMS and EMS and OHSAS 18001 system Standard? Have you establish the
Have you identified risk and opportunity and what action is planned and
22.
implemented for the same?
Are all employees are aware of all such precautions to reduce environmental
23.
impacts? How they become aware? Is there any periodical plan for such things?
How do you come to know that the pressure vessels / receivers and lifting tools
24.
and tackles are tested as per the factory acts, periodically?
25. Are your employees are aware of fire frightening and use of fire extinguishers?
Is access to such fire fighting equipments and personal protective equipments are
26.
open? Have you trained all employees for not to block such access way?
How are you disposing output wastages generated by your department? Where
27.
do you store such wastages?
How do you sold chemical contaminated packages? Is there any mechanism to
28. sell such packages after neutralizing it? Are you selling such products to the
authorized processor?
Are you having list of registered Re-processor/ Re cycler as required under
29.
compliance obligation?
30. What do you do for old batteries? How do you dispose it?
Who is authorized for periodic disposal of scrap? Are you having method of
31.
disposal of all such water / warn- out parts etc.?
Are you having material safety data sheet for all Raw Materials and finish
32. products manufactured by you? Are training related to MSDS is given to all
employees of your department?
33. Are all employees using personal protective equipments during routine activities?
What is the rate of accident? Are you maintaining documented information of
34. accident, near miss etc.? Is there any mechanism for review and analysis of
accidents, near miss etc.?
Have you defined requirements of temperatures, pressures, and other process
35. parameters during the production, which could directly/ indirectly affects
environment?
36. Are you having documented information for plant shut down and start – up?
Are you having emergency plant shut down documented information? Is this
37.
standard operating procedure is communicated to all employees?
Are you having defined and documented processes for each manufacturing
38.
activities for all products? Are care of environment is taken in all such processes?
What are the associated utilities are used by your department for manufacturing
39.
of products? Are there defined documented information for all such utilities?
Have you done loss analysis of such utilities, which directly affects environment /
40.
resources of your organization?
Are aspects identified and impact evaluated for all such utilities? Are you
41.
employees aware of all such aspects?
42. How do you come to know that the pressure vessels/receivers and lifting tools
6. Stores
Have you under gone training related to Material safety date sheet? Are your
1. employees trained for it? Are you having copy of all MSDS of
Row materials?
Have you defined stack height for raw materials stored by you? What is method of
2.
storage and handling through out the stores?
Do you know which two categories of chemicals cannot be stored together? What
3. is mechanism of storage of such raw materials? Are your all employees aware of
it?
Have you prepared Aspect / Impact register? What are the significant aspects of
4.
your department?
Where do you stare liquid materials? Do you have defined standard operating
5.
procedure for loading, unloading and storage for such liquid materials?
Where do you store solvents? Are they in open area? Whether “ No smoking “
6.
Board is displayed near solvent storage area?
Have you prepared Environmental aspects, OHS Hazards, impacts and risk
7. associated register? What are the significant aspect and OHS Hazards of your
department?
Where do you store waste oil / grease? Are such covered in Aspect register?
8.
What is the method of disposal of such waste oil / grease? To whom do you sold?
What is the care taken by you during receipt and issue of the materials from the
9.
stores?
Are your all raw materials stored on pallets? Is the method for Preserving material
10.
adequate? How do you take care for the preservation of materials?
What are the care taken by your during all your activities to prevent pollution?
How do you maintain account for job work materials send with gate pass? What
11.
types of controls are established to avoid deterioration of Quality of material
during storage? What controls are followed for self-life material used?
What are the objectives of your department? What is the plan to achieve it? Have
12.
your identified any EMP in your department?
Do you maintain proper inspection and test status for materials lying in store
area? Which methods are followed for receipt and issue of materials form store?
13.
Are you having persons list for the issue of materials for the same? How do you
maintain documented information for the issue and receipt of material?
How do you prevent, or reduce, undesired effects related to risk? Have you define
a quality risk assessment process? Show me. Have you update risks based on
14.
such investigation in documented information? Do you implement action from
risks and opportunities?
How do you identify uninspected, O.K. & not O.K. materials? How do you inform
15. concern department person for arrival of materials to carry out necessary
inspection? How do you control shelf life material?
Have you specified minimum inventory level at any place for critical items? Are
16. you involved in raising the indent for follow up of indent for the indent raised by
various departments? How do you keep tack for the pending indents?
What is the process approach in your department? What is the input in the
various activities done by you? Have you prepared Quantifiable criteria for your
17.
department to monitor the effectiveness? How do you monitor it? Have you
conveyed the same to the concerned staff members in your departments?
Are you having MSDS for all the chemicals stored in the raw materials stores?
How do you take care for the various symbols put on the packing of raw materials
18.
and what is the meaning of the same? Have you got any training for the safety
issues?
7. Engineering
Are you having preventive maintenance schedule? Are you having defined
preventive maintenance checking points for all equipments? Is it based on
manufacturer’s suggestions? Are you timely following it? Where is it documented?
1.
Are you having equipment history data? Are you maintaining breakdown
maintenance data? Are such checkpoints covers the quality and environmental
and occupational, health and safety issues considering operating condition?
Are you all moving parts covered by moving guard? Are you having any action
2. plan, where the guards are not there? Are you doing using personal protective
equipments? Is it verified?
What is the process approach in your maintenance activity? What is the input and
output in your various processes of your utilities as well as plants? Have you
prepared Quantifiable criteria for your department to monitor the effectiveness?
3.
How do you monitor it? Have you conveyed the same to the concerned person
like supervisors and workers? What is action plan for achievement of quantifiable
criteria? How do you achieve it?
Are you following methods for process control and process monitoring on utility
4.
equipment? What is the control parameter during the processes?
Have you prepared Aspect / Impact register as well as Hazard and risk records
considering your all activities? Are you having any significant aspects? Are you
5.
having plans in your department? Do you monitor the progress on such plan?
How?
Have you prepared Environmental aspects, OHS Hazards, impacts and risk
associated register considering your all activities? Are you having any significant
6.
aspect and OHS Hazards? Are you having OHSMP and EMP in your
department? Do you monitor the progress on such EMP? How?
Where do you store maintenance wastes, waste oil and grease? How do you
7.
dispose such waste? To who do you sold waste oil and grease?
Where do you store maintenance wastes, waste oil and grease? How do you
8.
dispose such waste? To who do you sold waste oil and grease?
What are utilities operated and controlled by you? Which type of waste generated
9.
during operation of such utilities? Where do you dispose such waste?
Are you having aspects / Impacts for all such utilities and waste disposal and your
10.
activity? What are your significant aspects and what actions taken for the same??
Do you have system of work permit? Who is authorized to issue work permit? Is
11.
there any standard operation procedure for such work permitting system?
Are you having all PPEs considering type and nature of work done by you? How
12.
do you issue such PPEs to your employees?
Is there appropriate control of materials, equipment and critical parameters of
13. utility process? How do you monitor and control your processes? Are you
maintaining documented information for process control monitoring?
Have you attended management review meetings? What was discussion related
14. to your areas? Have you completed actions decided in management review
meeting in your area?
Have you define a quality risk assessment process? Show me.
15. How do you prevent, or reduce, undesired effects related to risk? Do you
implement action from risks and opportunities? Have you update risks based on
such investigation in documented information?
What competence, education and experience are required for your employees?
16. What have your documented it? Based on that any gap is found in your
department? How do you maintain the documented information for the same?
How do you ensure competence of persons performing work affecting the
17. Quality? What kind of infrastructure do you provide? How do you identify and
convey your need your need for the resources?
How do you get information for the customer requirements and ensure its
8. fulfillment? Are you inspecting reprocessed material? Show us documented
information?
Are you carrying out testing of all the critical incoming material, in process and
9. final stages for each lot? How do you maintain documented information? How do
you maintain status of inspection?
What action have you taken after receiving customer complaints? How do you
10.
analyse customer complaints?
How do you ensure that product has passed through all the inspection & meet
customer requirements? How do you carry out final inspection of product to be
11.
supplied to different segment like replacement market, defence, exports etc.?
Where are you keeping documented information?
Have you attended management review meetings? Which was discussion related
12. to your areas? Have you completed actions decided in management review
meeting in your area?
How do you get special test requirements of customers and how it is carried out?
13. Do you get any test method for testing of product from the customer? How do you
follow it?
How do you maintain master list of documented information with retention period?
All type of documented information including computerized documented
14. information maintained by you is covered in the master list of documented
information? In your all the files record name and format no. (If applicable) is
written? Proper document control is established by you?
Have you been audited? How many NCR’s given to you? Have you taken actions
15.
to close the same?
Are you using any subjective criteria for inspection and testing? How do you
16.
establish control for the same?
What is the process approach in your department? What is the input and output in
your laboratory? Have you prepared Quantifiable criteria for you area? How do
17.
you monitor it? Have you conveyed the same to the concerned person? Have you
prepared any action plan for the achievement of Quantifiable criteria?
18. How do you carryout process audit?
How do you prevent, or reduce, undesired effects related to risk? What is
19. significant environmental aspect in your areas and what action is taken for the
same?
Have you define a risk assessment process? Show me. Have you covered all
20.
issues and periodically monitoring it?
What are the things you consider in your department at the time of change in
21.
organization?
Is there necessary infrastructure and environment in your department for the
22.
operation of process?
23. Do you implement action from risks and opportunities?
24. Have you update risks based on such investigation in documented information?
10. Marketing
How do you carryout marketing of your product? Are you having agents? How do
1. you select such channel of distribution? Who is authorised for selection of them?
Are you having list of approved Dealer / Agent list for the same?
Have you prepared your company brochure? Are you having price list? Who
2.
approve it? How do you finalize price for the new product?
How do you participate in defining requirements for new products? How do you
3. get information for new products? How do you provide information for your
product to you customer as well as plant people?
Have you define customer expectations & product requirements? How do you
4.
communicate it to Design, Manufacturing, Q.C., packing etc?
How do you sale your products? How do you understand requirements related to
the products as below:
1. Requirements specified by the customer.
2. Requirements not specified by the customer for intended use.
3. Statutory and regulatory requirements applicable to the product.
5.
4. Any additional requirements considered necessary by the organisation.
Can you show us evidence that above 4 types of requirements is determined,
understood before execution of order? How do you ensure your capability for the
above requirements? How do you maintain contract review report? How do you
keep tract for completion of order and compilation of all such orders?
What are the Quantifiable criteria for your department? How do you monitor it?
Have you given any further criteria for your other sales staff? What process
6. approach do you adopt? What is input and output of your department? Have you
done any analysis for timely completion of orders or delay is delivery? How do
you amend the order?
How do you monitor effectiveness of department? Can you show us your action
7. plan for achievement of your quantifiable criteria? How do you monitor your
results for achievement of Quantifiable criteria vs. planned action?
How do you know plant capability for manufacture of different types of product?
How do you given delivery schedule? Have you done internal contract review any
8. time? Where are contract review report? How do you convey the same to the
plant? How do you confirm capability for new product development with the
customer as well as convey the same to plant?
What are the things you consider in your department at the time of change in
9.
organization?
How do you handle customer complaints? Any documented information are
maintained? When do you close such complaints? How fast you close the
10. customer complaints? Have you done any analysis for customer complaints and
warranty claims attended by the company? What corrective actions are taken for
the same?
How do you convert customer inquiry in to contract? Does the total requirements
11.
laid down?
12. How do you prevent, or reduce, undesired effects related to risk?
How do you identify country specific legal requirements at inquiry or order
13.
finalization stages?
14. Have you define a quality risk assessment process? Show me.
Is there necessary infrastructure and environment in your department for the
15.
operation of process?
16. Do you implement action from risks and opportunities?
Who has attended management review meeting? Have you decided any action
17. for your department? How? Does marketing monitor & report customer feedback
in management review meeting?
18. How do you maintain documented information in your area ?
Have you been audited? How many NCRs are given to you? Have you taken
19.
actions to close the same?
Have you update risks register based on such investigation in documented
20.
information?
How do you determine and implement effective arrangements for communicating
customers for product information (List of your brand products), order handling,
21.
complaints etc. Have you fixed any timeframe for the effective communication
with customer?
How do you measure customer satisfaction? Have you defined methods for the
same? Have you analysed such data? Have you taken any corrective action for
22.
the same? What is input for customer satisfaction survey? Have you fixed any
criteria for customer satisfaction?]
11. Purchase
Have you selected vendor and suppliers? Have you prepared Approved Vendor
1. List? What is a selection criterion? Do you maintain documented information for
AVL & Vendor selection/ evaluation?
How do you prevent, or reduce, undesired effects related to risk for your
2.
vendors/subcontractors?
What are the things you consider in your department at the time of change in
3.
organization?
4. Have you update risks based on such investigation in documented information?
Have you prepared any questionnaire for selection of vendor? Can you show the
5.
same?
Have you prepared clear specification for all the purchase items? How do you get
information on purchasing data form user department? Have you prepared
purchase specification for raw materials and are you referring the same document
6.
in the purchase order? How are you getting details for the spares and hardware
and job work items? How are you getting specification for the same? How do you
give codification for part number?
Have you made agreement for quality assurance with your subcontractor? Have
7. you established any control on them? How do you select subcontractor for job
contract? How do you establish control on them?
Can you show me documented information for the trial run or sample approval for
8.
the vendor selection/evaluation?
How do you ensure that outsourced process is controller or influenced. What type
and extent of control or influence is applied to the Process is defined within the
9. EQHSMS for such outsourced process? Have you established system for
selection of vendors and outsourced activities and how do you communicate such
controls to them?
Have you done periodic evaluation and vendor rating of your supplier? Which
10.
items are included for the same?
How do you carry out cash purchase? Who is authorised to purchase against
11.
letter of indent?
Is there necessary infrastructure and environment in your department for the
12.
operation of process?
Who is reviewing and approving purchase order for adequacy of the specified
13. requirements prior to release? Where is the list of authorised person for the
same?
How do you carry out purchase of service like labour contract, calibration of
14. instrument, transport etc.? Do you prepare P.O.? Contract / work order for the
same?
Are you going to vendor’s place for inspection of the product and are you
15.
conveying vendors for test certificate requirement as required by you?
How do you keep track for requirement vs. purchase order release vs. materials
receipt and monitor your purchase activity? How do you keep track for pending
16. requirements and describe purchase order cancellation procedure? How do you
keep track for pending purchase order? How do you amend the purchase order?
Show us documented information?
Are you using any vendor’s standard documents or master sample and who is
17.
controlling the same?
18. Do you Out sourced any of the processes?
19. How do you control the subcontracted processes?
Have you been audited? How many NCR’s are given to you? Have you take
20.
actions to close the same?
21. Do you implement action from risks and opportunities?
Have you attended management review meetings? What was discussion related
22. to your areas? Have you completed actions decided in management review
meeting in your area?
Have you documented job description with authority and responsibility to all the
23.
concerned persons in your department?
What is the process approach in your department? What is the input and output in
your various activities done by you? Have you prepared Quantifiable criteria for
your department to monitor the effectiveness? How do you monitor it? Have you
24.
conveyed the same to the concerned person staff members in your department?
What is action plan for achievement of quantifiable criteria? By which data? What
is action plan for the same?
What kind of communication process is established within the organisation? How
the communication takes place regarding the effectiveness of Quality
25.
Management System? Have you made any documented information for the
same? How is it implemented?
How do you control and store materials in the packing area? Have you identified
14.
areas for storage of different materials? How do you maintain stock for the same?
What is input to your department? What is output from your department? Have
15.
you identified any Quantifiable criteria? How do you monitor the same?
What are the things you consider in your department at the time of change and
16.
what is the change management process followed by you?
Is there necessary infrastructure and environment in your department for the
17.
operation of process?
How do you plan for trial production, R & D experiments and new jig development
11. during R & D stage? Where do you maintain the documented information? How
do you monitor performance of the trial run?
Hoe do you document design output covering information related to purchase,
production etc. Where do you document acceptance criteria for the products?
12.
How do you ensure product application for example paper, textile, plastic etc. for
the various pigments developed by you?
Where do you document stages of design review in the design plan? How do you
carry out design review? Who are the team members for the design review? Are
13.
you making any action plan? Where do you document information results of
review?
How do you carry our design and development verification? Before releasing the
14. product from laboratory are you documenting product specification in documented
form? How do you monitor the same?
How do you validate the design? Where do you maintain the documented
15.
information for the same?
Is there necessary infrastructure and environment in your department for the
16.
operation of process?
What is the different document generated from your departments? How do you
17.
establish control for design and development changes?
What is the process approach made by you? What is input to your department?
What is output from your department? How do you monitor your quantifiable
18.
criteria? How do you analyse results? What is action plant for achieving the
same?
When do you take corrective actions for the effect of the potential problems? How
19. do you determine potential nonconformities and their causes? How do you
document information results of action taken?
20. Do you implement action from risks and opportunities?