Job Type: Perm
Job ID: JO-1908-19265
Consultant: Karen McHugh
Are you an Analyst with 2+ years experience working in a GMP pharma environment?
Do you have HPLC, method development and optimization experience?
If you have the relevant experience, please forward your CV to firstname.lastname@example.org for review or call 353 1 7978720 to discuss in confidence.
QC Analyst - HPLC - Biopharma - Athlone
Our client is a leading Contract Research Organization (CRO), working with pharmaceutical, biotechnology and medical device sectors.
The role will primarily involve supporting method development and optimization activities for finished product testing, transfer and validation according to regulatory guidelines and may include routine testing for example dissolution and HPLC testing.
A degree in Chemistry or a related discipline is required
HPLC and dissolution experience is essential
Method development and optimization experience is required
A minimum of 2-3 years’ experience in a GMP pharma environment
Experience with technical transfers and validation is desirable
Demonstrate problem solving in delivering process and analytical understanding.
Good understanding of requirements for working in a GMP environment.
Good understanding of Empower 3 Software
Ability to quickly learn new processes.
Ability to communicate clearly and to form strong working relationships with colleagues.
Ability to work on own initiative and be capable of developing solutions to problems
Willing to operate in a flexible manner and be able to switch priorities at short notice.
Good team player, organised, accurate, have strong documentation skills.
Passionate about quality and customer service.
Good communication skills both internally and externally.
Permanent Full time position
Benefits include medical insurance, pension and life assurance.
Karen McHugh is the consultant managing this position.
If you have any queries about this role, you can contact him by e-mail email@example.com or phone +353-1-7978720
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