Job Details: Quality Executive


JobsIreland
Jervis Street
Dublin 1
jobsireland.ie
Quality Executive
JOB DESCRIPTION

QUALITY EXECUTIVE Quality Process Management and Support (QPMS)

My client, a Pharmaceutical manufacturing company based in Dublin have
a new opportunity for a Quality Executive to join the team. Your role
will become a part of building a strategically important global
function for the company.

By joining this organisation, you will get the opportunity to create
results, develop yourself among highly skilled colleagues while taking
on their common quest to become the preferred care partner improving
peoples lives around the world.

Your new role

As a Quality Executive in the QPMS department, you will report to the
QPMS Department Manager.

The successful candidate will be responsible for a range of GMP
Activities which may include the following

Ownership of quality systems on site; training, oversight and
implementation

Quality SAP Master Data input

Produce and provide reports and metrics for review

Updates to certificates of analysis and specifications for raw
materials and finished products

Manage the service provider inspection program on site

Provide GMP Training as required

Provide regulatory support as required

Participate in GMP inspections by partners and regulatory authorities

Support the Customer Complaint process

Collate information and assist in the preparation of reports in
relation to Annual Product Reviews for all products manufactured on
site.

Liaise with other Department representatives to promote improvements
in GMP and Quality standards.

Keep abreast of latest developments from Regulatory Authorities

Support and deliver continuous improvements and to employ problem
solving tools including root cause analyses and CAPA identification.

Qualifications & Experience:

A minimum of an honours degree in Chemistry, Biology, Engineering or
equivalent third level degree qualification.

SAP and Track Wise experience are an advantage.

At least three years experience in a quality or manufacturing function
within the pharmaceutical industry.

Strong understanding of pharmaceutical quality processes and systems,
manufacturing processes and other support/control systems is
desirable.

The successful candidate will be a demonstrated self-starter with a
proactive, hands-on approach, possessing excellent interpersonal,
decision-making, teamwork, and communication skills.

They will be capable of delivering to tight and often multiple
deadlines in a dynamic, challenging work environment.

For full details, contact Tina on +**Apply on the website** or **Apply
on the website** or email (Please contact us using the "Apply for this
Job Posting" box below)

Thornshaw Scientific is a division of the CPL group. Log on to for a
list of active vacancies
JOB DESCRIPTION

QUALITY EXECUTIVE Quality Process Management and Support (QPMS)

My client, a Pharmaceutical manufacturing company based in Dublin have
a new opportunity for a Quality Executive to join the team. Your role
will become a part of building a strategically important global
function for the company.

By joining this organisation, you will get the opportunity to create
results, develop yourself among highly skilled colleagues while taking
on their common quest to become the preferred care partner improving
peoples lives around the world.

Your new role

As a Quality Executive in the QPMS department, you will report to the
QPMS Department Manager.

The successful candidate will be responsible for a range of GMP
Activities which may include the following

Ownership of quality systems on site; training, oversight and
implementation

Quality SAP Master Data input

Produce and provide reports and metrics for review

Updates to certificates of analysis and specifications for raw
materials and finished products

Manage the service provider inspection program on site

Provide GMP Training as required

Provide regulatory support as required

Participate in GMP inspections by partners and regulatory authorities

Support the Customer Complaint process

Collate information and assist in the preparation of reports in
relation to Annual Product Reviews for all products manufactured on
site.

Liaise with other Department representatives to promote improvements
in GMP and Quality standards.

Keep abreast of latest developments from Regulatory Authorities

Support and deliver continuous improvements and to employ problem
solving tools including root cause analyses and CAPA identification.

Qualifications & Experience:

A minimum of an honours degree in Chemistry, Biology, Engineering or
equivalent third level degree qualification.

SAP and Track Wise experience are an advantage.

At least three years experience in a quality or manufacturing function
within the pharmaceutical industry.

Strong understanding of pharmaceutical quality processes and systems,
manufacturing processes and other support/control systems is
desirable.

The successful candidate will be a demonstrated self-starter with a
proactive, hands-on approach, possessing excellent interpersonal,
decision-making, teamwork, and communication skills.

They will be capable of delivering to tight and often multiple
deadlines in a dynamic, challenging work environment.

For full details, contact Tina on +**Apply on the website** or **Apply
on the website** or email (Please contact us using the "Apply for this
Job Posting" box below)

Thornshaw Scientific is a division of the CPL group. Log on to for a
list of active vacancies


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Type: Permanent
Payment:
Category: Others

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