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INTE

R

N

A

L

A

UD

IT

PR

OCE

DUR

E

BOS-

P

RD-1202.90020

3

x

T

o

conf

i

rm

the author

i

ty

to

conduct

the aud

i

t

;

x

T

o prov

i

de

i

nformat

i

on

on

the proposed

t

i

m

i

ng and Aud

i

t

T

eam

compos

i

t

i

on

;

x

T

o

re

q

uest access

to

re

l

evant documents

, i

nc

l

ud

i

ng

records

;

x

T

o determ

i

ne app

li

cab

l

e

s

i

te

safety and

secur

i

ty

ru

l

es

;

x

T

o ma

k

e arrangements

for

the aud

i

t

;

and

,

x

T

o announce an

eventua

l

attendance

of

O

bservers

and

the

need

for

G

u

i

des

for

the Aud

i

t

T

eam

.

4.

3

C

onducting document

re

v

iew

T

he

A

uditee

’

s

documentat

i

on

shall

be

rev

i

ewed

to

determ

i

ne

the

conform

i

ty

of

the

system

,

as

documented

,

w

i

th

aud

i

t

cr

i

ter

i

a

. T

he

documentat

i

on

shall

i

nc

l

ude

re

l

evant management

system

documents

and

records

,

and

prev

i

ous

audit reports

. T

he

rev

i

ew

shall

ta

k

e

i

nto account

the ob

j

ect

i

ves

and

scope of

the

aud

i

t

.

I

f

the

documentat

i

on

i

s

found

to

be

i

nade

q

uate

,

the

QM

S

A

udit

T

eam

Leader

shall

i

nform

the

A

uditee

,

and

the

Q

ua

l

it

y

Re

p

resentati

v

e

.

A

dec

i

s

i

on

should

be

made

as

to

whether

the

Q

M

S

aud

i

t

should

be

cont

i

nued

or

suspended unt

il

documentat

i

on

concerns

are

reso

l

ved

.

4.4

Pre

p

aring

for

t

h

e on-site

audit acti

v

ities

4.4.1

Pre

p

aring

t

h

e

audit

pl

an

T

he

QM

S

A

udit

T

eam

Leader

shall

prepare

the

Audit Plan

to

prov

i

de

the

bas

i

s

for

the

agreement

among

the

A

uditee

and

the

Q

M

S

Aud

i

t

T

eam

regard

i

ng

the

conduct

of

the

Q

M

S

aud

i

t

. T

he

p

l

an

shall

fac

ili

tate

schedu

li

ng

and

coord

i

nat

i

on

of

the aud

i

t act

i

v

i

t

i

es

.

T

he

amount

of

deta

il

prov

i

ded

i

n

the

Audit Plan shall

ref

l

ect

the

scope

and

comp

l

e

xi

ty

of

the

aud

i

t

. T

he

Audit Plan

shall

be

suff

i

c

i

ent

l

y

f

l

e

xi

b

l

e

to

perm

i

t

changes

,

such

as

changes

i

n

the

aud

i

t

scope

,

wh

i

ch

can

become

necessary

as

the on

-

s

i

te

Q

M

S

aud

i

t

act

i

v

i

t

i

es

progress

.

x

T

he

Audit Plan shall

cover

the

fo

ll

ow

i

ng:

x

T

he aud

i

t

ob

j

ect

i

ves

;

x

T

he

Q

M

S

aud

i

t

cr

i

ter

i

a and

any

reference documents

;

x

F

or

an e

x

terna

l

supp

li

er

aud

i

t

,

the

“

ISO 9001

standard

”

shall

be

used

at

l

east

;

x

T

he use of

spec

i

f

i

c

chec

kli

sts

i

f

needed

(

e

.

g

.

supp

li

er

,

mann

i

ng and

crew

sourc

i

ng

,

etc

.);

x

T

he

Q

M

S

aud

i

t

scope

, i

nc

l

ud

i

ng

i

dent

i

f

i

cat

i

on

of

the

O

rgan

i

zat

i

ona

l

and

funct

i

ona

l

un

i

ts

and

processes

to

be

aud

i

ted

;

x

T

he

Q

M

S

aud

i

t

samp

li

ng

cr

i

ter

i

a

;

x

T

he dates

and p

l

aces where

the

on

-

s

i

te aud

i

t act

i

v

i

t

i

es

are

to

be

conducted

;

x

T

he

e

x

pected

t

i

me

and

durat

i

on

of

on

-

s

i

te

Q

M

S

aud

i

t

act

i

v

i

t

i

es

, i

nc

l

ud

i

ng

meet

i

ngs

w

i

th

the

A

uditee

’

s

management and Aud

i

t

T

eam meet

i

ngs

;

x

T

he

ro

l

es

and

respons

i

b

ili

t

i

es

of

the

QM

S

A

udit

T

eam members

and accompany

i

ng

persons

;

x

T

he a

ll

ocat

i

on of

appropr

i

ate

resources

to

cr

i

t

i

ca

l

areas

of

the aud

i

t

;

x

I

dent

i

f

i

cat

i

on of

the

A

uditee

’

s

representat

i

ve

for

the

aud

i

t

;

x

T

he

wor

ki

ng

and

report

i

ng

l

anguage

of

the

aud

i

t

where

th

i

s

i

s

d

i

fferent

from

the

l

anguage

of

the

A

uditor

and/or

the

A

uditee

;

x

T

he aud

i

t

report

top

i

cs

;

x

L

og

i

st

i

c

arrangements

(

trave

l,

on

-

s

i

te

fac

ili

t

i

es

,

etc

.).

T

he

Audit Plan shall

be

comp

l

eted

and

agreed by

the

QM

S

A

udit

T

eam

Leader

(and

e

v

entua

lly

t

h

e

A

udit

Cl

ient

)

and

the

A

uditee

between

1

5

and

3

0

days

pr

i

or

the

f

i

rst

aud

i

t

day

. F

urther

changes may

occur

but

shall

have

a

ll

part

i

es

’

agreement

.

Any ob

j

ect

i

ons

by

the

A

uditee

shall

be

reso

l

ved

between

the

QM

S

A

udit

T

eam Leader

and

the

A

uditee

.

Any

rev

i

sed

Audit Plan shall

be

agreed

among

the

part

i

es

concerned

before

cont

i

nu

i

ng

the aud

i

t

.

Vers

i

on

SF (BOS-

P

RD-1202.0001-

ver

.0

4

). O

r

i

g

i

na

l

date:

2011-0

3

-2

3

.

Vers

i

on

date:

201

5

-12-10.

Va

li

d

vers

i

on

on

l

y

on

Q

M

S

s

i

te

.

Uncontro

ll

ed

document

when

pr

i

nted

.

Procedure prepared by:

BOS

Aud

i

t Manager

.

Approved

by:

BOS Q

H

S

E Manager

.

Va

li

dated by:

BOS Q

ua

li

ty

R

epresentat

i

ve

.

Page

7

of

20

977