Are you a QC Analyst with experience in a one or more of the following QC activities; Reagent management, media preparation, GMP document review and management, sample and data management and some analytical testing?
This is a contract role based in Dublin.
If you have the relevant experience, please forward your CV to View email address on jobcontax.com for review or call Show phone number to discuss in confidence.
QC Analyst - Bioanalytical Sciences - 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 on 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.
Additionally, the role may involve carrying out additional work functions that are not described in this specification but are associated with their role.
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.
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 Techniques
Requirements
Bachelor’s degree in a science discipline.
1-2 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.
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)
Package
Contract role
Hourly Rate €20 - €25 per hour
Minimum 12 month contract
Contact
Karen McHugh is the consultant managing this position.
If you are a QC Analyst interested in roles based in Dublin, you can contact Karen by e-mail View email address on jobcontax.com or phone Show phone number for a confidential chat.
JobContax do not send CVs to clients without candidate permission.
With over 50 years of technical recruitment experience, JobContax is the leading recruiter of QC Analyst s in Dublin and Ireland.
Due to the large volume of applications, JobContax may not be able to respond to every individual.
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