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Correcti

v

e

A

ction

P

rocedure

BOS-PRD-1201.901201

4

.

2

.

4

A

udit correcti

v

e

a

ction

A non-conformity or observation detected during an Audit

shall

be reported in the

Description of Non-

Conformities and Observations

form. The

A

udit Te

a

m

is responsible for describing the situation.

Once the non-conformity or observation is described, the

A

udit Te

a

m Le

a

der

shall

grade in the

Description

of Non-Conformities and Observations

(as part of the Audit Report) as:

x

An observation;

x

A minor non-conformity;

x

Or a major non-conformity.

These conclusions and their supporting audit evidences

shall

be kept and recorded onboard and at the Head

Office.

Once graded, conclusions

shall

be reviewed with the

A

uditee

to obtain acknowledgement that the audit

evidence is accurate, and that the non-conformities and observations are understood. Every attempt

shall

be

made to resolve any diverging opinions concerning the audit evidence and/or findings, and unresolved points

shall

be recorded.

As indicated in the

Internal Audit Guidelines,

the Audit Report illustrates the record evidence of the

conducted audit against the

A

uditee

’s Management System. The

A

udit Te

a

m

shall

present the Audit

Report at the end of the closing meeting in order that the

A

uditee

shall

keep the necessary

information which

shall

allow to immediately identify which corrective actions

shall

be taken to

improve its Management System.

When an observation is detected and understood, the

A

udit Te

a

m Le

a

der

and the

A

uditee

shall

issue a

recommendation for improvement. Recommendations issued from Observations are not binding, although

they represent an opportunity for improvement.

Once understood, minor and major non-conformity

shall

be reviewed by the

A

uditee

and the

A

udit Te

a

m

Le

a

der

for formal agreement. Both

shall

agree, or not, the non-conformity. If the non-conformity is not

agreed, an appeal

shall

be attached to the Audit Report. The appeal and the Audit Report

shall

be sent to

the

Q

H

S

E

S

M

a

n

a

ger

,

P

roce

ss

O

w

ner

a

nd/or De

s

ign

a

ted

P

er

s

on

A

s

hore

depending of the source of the

audits who

shall

determine the need for an audit corrective action. Once agreed, an audit corrective action

shall

be issued by the

A

uditee

. Feedback

shall

be provided to the

A

uditee

of any non-conformity and if

appropriate to other areas within the Organisation.

4

.

3

Detecting

a

nd

a

n

a

l

y

s

ing c

a

u

s

e

s

Each non-conformity or deviation

shall

originate a root cause analysis to establish a corrective action.

A root cause is a source of a deviation or non-conformity, which if removed or mitigated will

respectively disappear or decrease to acceptable levels.

The

P

roce

ss

O

w

ner

shall

designate an

I

mplement

a

tion Re

s

pon

s

i

b

le

in order to identify the root cause.

TapRooT

TM

methodology, which combines incident identification, analysis, and dynamic report,

shall

be used

for investigating all incidents. In this case, the

I

mplement

a

tion Re

s

pon

s

i

b

le

, designated by the

P

roce

ss

O

w

ner

,

shall

be in charge of the root cause analysis in TapRooT

TM

.

The

I

mplement

a

tion Re

s

pon

s

i

b

le

shall

have the necessary competence, availability and legitimacy to

implement the corrective action. He/she

shall:

x

Assess and analyse the cause(s) of each deviation, non-conformity and/or incident raised;

x

Measure the impact of each cause(s) detected;

x

Identify a corrective action per non-conformity, deviation or incident generated to prevent

reoccurrence;

x

Ensure the Management of Change when applicable;

x

Determine an action plan with due date.

Version 02. Original date: 05/06/2012. Version date: 31/12/2014. Valid version only on QMS site. Uncontrolled document when printed.

Procedure prepared by: BOS QHSES Manager. Approved by: Quality Director of BOURBON. Validated by: Quality Director of BOURBON.

This QMS document is validated as compliant to BOURBON standards (

http://intranet.bourbon-online.com/QMS )

.

8 /13

Transposition from Corporate original (last

version date:07/08/12)

729