Job Details: QC Analyst - Lab Testing - Dublin


jobContax

104 Upper Drumcondra Road,
Dublin 9
http://www.jobcontax.com
Please contact: Karen
JobContax was founded in 2001 by Karen McHugh, an engineer passionate about offering quality opportunities to the jobseeker and an intelligent service to the client. Jobcontax has successfully operated as a global market leader and technical specialist within the following sectors:

Construction and Infrastructure

Engineering and Design

Mining - Oil and Gas

Biotechnology and Pharmaceutical

During the past 10 years Jobcontax have expanded our international network across 5 continents. In 2005 we began recruiting for the Australian market and in 2011 we set up our first strategic partnership in WA. In March 2010, we opened our Shanghai office to strengthen our presence in the rapidly expanding Chinese market for highly skilled professionals. JobContax has a strong presence in Canada, Europe and the Middle East.

Jobcontax has built its reputation on its consultative approach. Our understanding of the industries and the businesses and individuals within these industries enables us to facilitate the perfect match between client and jobseeker. From global multinationals to SME?, Jobcontax has become the trusted recruitment partner.
QC Analyst - Lab Testing - Dublin
Are you a QC Analyst with 2+ years experience in a wide variety of
analytical techniques including but not limited to Cell-Based Potency
Bioassays, Immunoassays, Cell Culture and Aseptic Technique?

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 - LAB TESTING - 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, responsible for one or more of the
following activities in QC including: Reagent management, media
preparation, GMP document review and management, sample and data
management and some analytical testing.

Contributes to team by ensuring the quality of the tasks/services
provided by self.

Contributes to the completion of milestones associated with specific
projects or activities within team

The role undertakes implementing continuous improvement projects and
supporting a lean culture and Right First Time (RFT). 

The role also represents the QC unit by liaising with internal and
external customers.

With a high degree of technical flexibility, work across diverse areas
within the lab

Plan and perform routine tasks with efficiency and accuracy.

Review, evaluate, back-up/archive, and approve analytical data.

Troubleshoot, solve problems and communicate with stakeholders.

Participate in audits, initiatives, and projects that may be
departmental or organizational in scope.

Evaluate lab practices for compliance and operational excellence
improvement on a continuous basis.

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

Bachelor’s degree in a science discipline.

2+ years of biopharmaceutical QC experience or related quality control
or GMP laboratory experience in the pharmaceutical or medical device
industry.

Experience with regulatory compliance in cGMP manufacturing and
testing of pharmaceutical products.

Demonstrated ability to work independently and deliver right first
time results

Works under minimal direction 

Work is guided by objectives of the department or assignment

Follows procedures

Refers to technical standards, principles, theories and precedents as
needed

May set project timeframes and priorities based on project objectives
and ongoing assignments. Recognizes and escalates problems

Demonstrated leadership and communication skills

Auditing documentation and operation process

Demonstrated ability to interact with regulatory agencies

Understanding and application of principles, concepts, theories and
standards of GMP QC analytical laboratories. 

Deepens technical knowledge through exposure and continuous learning

Knowledge of related regulatory/industry considerations, compliance
issues and/or scientific discovery

Some / limited experience in a wide variety of analytical techniques
including but not limited to Cell-Based Potency Bioassays,
Immunoassays, Cell Culture and Aseptic Technique

Take initiative to identify and drive improvements

Excellent verbal and written communication skills

Strong Technical writing skills for GMP documentation (e.g.
investigations, procedures, change controls)

Presentation skills

Escalate issues professionally and on a timely basis

Decision Making skills

Teamwork and Coaching others

Negotiation and Influence skills

Project Management and organizational skills, including ability to
follow assignments through to completion

PACKAGE

Contract role

Hourly Rate € * - € *
per hour

Minimum * month contract

Onsite requirement is 5 days a week as this is a lab-based role.

There are no shift requirements.

The core working hours are *:**Apply on the
website** to *: *.



We need : English (Good)

Type: Permanent
Payment: EUR 25 - 32 Per Hour
Category: Construction

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Email: (*) 
Phone: (*) 
Please Provide a Cover in the English Language.
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