QC Chemistry Analyst

HERO

Job Detail

Location Limerick Limerick
Salary Negotiable
Posted
Role Type Fixed Term Contract
Contact Katie Kilbane
email network@hero.ie

QC Chemistry Analyst

Apply Now

Job ID: JOB-12867

QC Chemistry Analyst

Limerick

Finding the right company that aligns to your career aspirations and values is so important. It’s worth taking the time to get this right. This QC Chemistry Analyst job opportunity located on the outskirts of Limerick city is one of those stand out positions that don’t come along every day. Let us tell you more….

 

Our client is a market leader, and as a QC Chemistry Analyst you will be required to perform a wide variety of analytical chemistry tests to support in-process and bulk drug substance manufacturing in a cGMP regulatory environment.

 

Responsibilities:

Reporting to the QC Chemistry Lead, the person will be responsible for the following;

  • Performing a wide variety of analytical chemistry testing to support in process and bulk drug substance release.
  • Ensures that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs).
  • Completes own test records on time and peer reviews data from other analysts for accuracy and completeness.
  • Maintains laboratory reagents and supplies.
  • Calibration of laboratory instruments.
  • Participates in the transfer of methodology from other test facilities.
  • Provides support and advice to manufacturing on QC related topics.
  • Conducts laboratory investigations and generates reports in response to invalid assays, Deviations, OOS/OOT.
  • Initiates and completes CAPAs and Change Controls in accordance with site procedure.
  • Writes new and updates current SOPs as needed.
  • Provides training to other analysts in the QC group.
  • Presents analytical data reports clearly and concisely to management.
  • Proactively identifies and implements lab process improvements, lean initiatives.
  • Performs other duties relevant to the QC laboratory position as required.


Requirements:

  • A third level qualification in a scientific/technical discipline.
  • At least 1 year hands-on work experience in a regulated QC laboratory-testing environment within the biopharmaceutical/pharmaceutical industry.
  • Excellent Communication skills, both verbal & written.
  • Experience with electronic systems such as LIMS, Empower, Qumas, eDoc, Trackwise etc., is an advantage.
  • Adaptable and flexible, willing to travel when needed.
  • Collaboration and team work. Maintains the highest standards of ethical behaviour.
  • Results and performance driven.
  • Strong analytical ability and associated problem solving.
  • Good time management and attention to detail.
  • Knowledge and proficient in the use of Microsoft products including, Excel, Word and PowerPoint.


Preferred Laboratory Experience in one or more of the following areas:

  • Analytical
  • HPLC
  • UPLC
  • UV-Vis spectrophotometry
  • Densitometry
  • Wet chemistry testing techniques including pH, conductivity, appearance and osmolality
  • Familiar with USP, JP and EP methodology.


Benefits:

  • Competitive base salary
  • Health Insurance for you and your family
  • Dental & Optical care
  • Pension Scheme
  • Bonuses
  • 26 days holidays
  • Onsite Gym
  • Subsidized meals

 

For further information on this role please contact Katie Kilbane on 086 1283368  / network@hero.ie

 

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

 

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

 

Katie Kilbane

JOB-12867

Apply Now

QC Chemistry Analyst

Katie Kilbane

Role Type Fixed Term Contract
Contact Katie Kilbane
email network@hero.ie
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