microbiology lab?
This is a contract role based in Dun Laoghaire, Dublin.
If you have the relevant experience, please forward your CV to **Apply
on the website** for review or call *-**Apply
on the website** to discuss in confidence.
QC ANALYST - MICROBIOLOGY LAB - DUBLIN
JOB DESCRIPTION
Our client is a leading international Biotechnology company with a
state of the art aseptic manufacturing facility in Dun Laoighaire,
South Dublin.
The plant is one of the most dynamic in Ireland and is currently
undergoing rapid expansion and capital investment.
This is an excellent opportunity to get experience into
Ireland&# *;s leading aseptic manufacturing
plant.
Under minimal supervision, successful candidate would be responsible
for one or more of the following activities in QC including
microbiological testing, method transfers, sample and data management
and equipment maintenance.
This role is for an experienced and technically strong associate who
will spend *% of their work day performing
testing.
The successful candidate would contribute to team by ensuring the
quality of the tasks/services provided by self and contribute to the
completion of milestones associated with specific projects or
activities within team.
This role will support manufacturing operations, as such some extended
hours, shift and weekend work may be necessary as required.
Endotoxin testing of water, in-process and drug product release
samples
Bioburden testing of water & in-process drug product samples
Sterility testing
Water sampling
Lab Support duties such as Biological Indicator testing, Growth
Promotion, Media Preparation, Identifications and Autoclave.
Writing technical reports
Perform analytical testing as a main priority with efficiency and
accuracy
With a high degree of technical flexibility, work across diverse areas
within the lab
Plan and perform multiple routine/ non-routine methods and procedures
with a large variety of assays.
Report, evaluate, archive, trend and approve analytical data.
Troubleshoot, solve problems and communicate with stakeholders.
Initiate and/or implement changes in controlled documents.
Participate in audits, initiatives, and projects that may be
departmental or organizational in scope.
Write protocols and perform assay validation.
Introduce new techniques to the lab, including method transfers,
reports, validations and protocols.
Evaluate lab practices for compliance and operational excellence
improvement on a continuous basis.
Review and Approve lab results
May participate in lab investigations.
May provide technical guidance.
May train others.
May contribute to regulatory filings.
May represent the department/organization on various teams
May interact with outside resources
REQUIREMENTS
Bachelors degree in a science discipline
Biopharmaceutical QC experience in a microbiology lab
Experience with regulatory compliance in cGMP manufacturing and
testing of pharmaceutical products
Sterility testing
Proficient in identifications
NPI Validation Work
PACKAGE
Contract role
Hourly Rate € * - € *
per hour
Minimum * month contract
Days Role (Mon-Fri), however on-call is required to support Bioburden
testing at the weekend.
We need : English (Good)
Type: Permanent
Payment: EUR 25 - 32 Per Hour
Category: Construction
