are looking for a Quality Operations Manager to join their team.
The Company
A Global biopharmaceutical company focused on improving
patients&#**Apply on the website**; lives through commercialising
quality, innovative medicines prescribed by primary care physicians,
specialists and those who treat patients with rare diseases.
The company markets a portfolio of medicines through its orphan,
primary care and rheumatology business units. The company&#**Apply on
the website**;s global headquarters are in Dublin. The company also
has offices in the US and Europe. This role will be based in their
start-up manufacturing facility in Waterford.
The Position:
As a Quality Operations Manager you will be responsible for supporting
the maintenance and management the Pharmaceutical Quality System and
that it is consistently deployed and maintained for operations and
supporting functions.
_YOU WILL_ also initiate action to correct quality and or compliance
concerns, inform as appropriate through the Quality Leadership Team.
RESPONSIBILITIES:
Ensure review of all Quality and production batch documentation is
completed correctly, to achieve a high level of customer service and
cGMP
Ensure that Batch documentation, Laboratory results and related
Quality System documentation is correct and approved prior to QA/QP
release
Ensure customer / contract services Technical Agreements are
implemented and maintained according to established procedures
Provide support for management of complaints, deviations,
CAPA&#**Apply on the website**;s and change controls associated with
commercial products
_QUALIFICATIONS_ and Skills
REQUIRED:
Bachelor&#**Apply on the website**;s degree in chemistry, biology or a
related discipline is desirable.
7 years&#**Apply on the website**; experience working in Quality or
Manufacturing, with a minimum of 2 years in a sterile manufacturing
environment.
_EXPERIENCE WITH_ investigations, change controls and CAPAs.
Thorough understanding of quality systems and GMPs.
To find out more about Real please visit
Real Staffing, a trading division of SThree Partnership LLP is acting
as an Employment Agency in relation to this vacancy| Registered office
| 1st Floor, **Apply on the website** King William Street, London,
EC4N 7BE, United Kingdom | Partnership Number | OC(phone number
removed) England and Wales My client, a start-up biologics manufacturing facility in Waterford,
are looking for a Quality Operations Manager to join their team.
The Company
A Global biopharmaceutical company focused on improving
patients&#**Apply on the website**; lives through commercialising
quality, innovative medicines prescribed by primary care physicians,
specialists and those who treat patients with rare diseases.
The company markets a portfolio of medicines through its orphan,
primary care and rheumatology business units. The company&#**Apply on
the website**;s global headquarters are in Dublin. The company also
has offices in the US and Europe. This role will be based in their
start-up manufacturing facility in Waterford.
The Position:
As a Quality Operations Manager you will be responsible for supporting
the maintenance and management the Pharmaceutical Quality System and
that it is consistently deployed and maintained for operations and
supporting functions.
_YOU WILL_ also initiate action to correct quality and or compliance
concerns, inform as appropriate through the Quality Leadership Team.
RESPONSIBILITIES:
Ensure review of all Quality and production batch documentation is
completed correctly, to achieve a high level of customer service and
cGMP
Ensure that Batch documentation, Laboratory results and related
Quality System documentation is correct and approved prior to QA/QP
release
Ensure customer / contract services Technical Agreements are
implemented and maintained according to established procedures
Provide support for management of complaints, deviations,
CAPA&#**Apply on the website**;s and change controls associated with
commercial products
_QUALIFICATIONS_ and Skills
REQUIRED:
Bachelor&#**Apply on the website**;s degree in chemistry, biology or a
related discipline is desirable.
7 years&#**Apply on the website**; experience working in Quality or
Manufacturing, with a minimum of 2 years in a sterile manufacturing
environment.
_EXPERIENCE WITH_ investigations, change controls and CAPAs.
Thorough understanding of quality systems and GMPs.
To find out more about Real please visit
Real Staffing, a trading division of SThree Partnership LLP is acting
as an Employment Agency in relation to this vacancy| Registered office
| 1st Floor, **Apply on the website** King William Street, London,
EC4N 7BE, United Kingdom | Partnership Number | OC(phone number
removed) England and Wales
We need : English (Good)
Type: Permanent
Payment:
Category: Others
