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MSD QC Bioanalytical Senior Technician 
Ireland, Dublin 
39755170

11.08.2024

Job Description

What You Will Do:

Bring energy, knowledge and innovation to carry out the following:

  • Executing and Supporting routine analytical testing with assays such as HPLC Analysis (IEX, SEC, RPLC), UV analysis, Capillary Electrophoresis and a wide range of compendial methods on Release, In-process, Raw Materials and Stability samples.
  • Support technical writing tasks such as deviation, protocol, report and procedure authorisation.
  • Participate in continuous improvement and laboratory transformation projects.
  • Support GMP, EHS and audits on site.
  • Maintain good housekeeping and hygiene within the laboratory.
  • Calibrate and maintain all designated laboratory instruments.
  • Follow up-to-date practices with reference to pharmacopoeias, specifications, regulations and industry standards.
  • Ensure training is current for all job functions performed.
  • Maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.
  • Ensure that cGMP standards are maintained at all times.
  • Promote and participate the implementation and maintenance of the relevant safety programmes.
  • Maintain Operational Excellence/Lean Lab standards within the laboratory.
  • Support with various QC related Initiatives.

What skills you will need:

In order to excel in this role, you will more than likely have:

  • Science/Chemical Engineering/Biological Engineering.
  • 1 - 5 years experience in the Pharmaceutical industry.
  • Experience in performing Laboratory testing.
  • Relevant experience and skill sets in their area of expertise that adds value to the business; ideally in a manufacturing, preferably in a GMP setting.
  • Experience and critical skills in the area of expertise that add value to the business; ideally analytical biochemistry, in a GMP setting.
  • Knowledge of regulatory/ code requirements to Irish, European and International Codes, Standards and Practices.
  • Knowledge of cGMP & Laboratory Quality Systems.
  • Report, standards, policy writing skills required.
  • Lean Six Sigma Methodology experience.
  • Effective communication, presentation and interpersonal skills, to interface effectively with all levels of colleagues and with external customers in a team orientated manner.

So, if you are ready to:

Current Contingent Workers apply


Not Applicable


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.



A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.